WO2021127044A1 - Combinations - Google Patents
Combinations Download PDFInfo
- Publication number
- WO2021127044A1 WO2021127044A1 PCT/US2020/065409 US2020065409W WO2021127044A1 WO 2021127044 A1 WO2021127044 A1 WO 2021127044A1 US 2020065409 W US2020065409 W US 2020065409W WO 2021127044 A1 WO2021127044 A1 WO 2021127044A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- unsubstituted
- substituted
- alkyl
- group
- cancer
- Prior art date
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- 125000000623 heterocyclic group Chemical group 0.000 claims description 114
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Classifications
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5355—Non-condensed oxazines and containing further heterocyclic rings
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/63—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide
- A61K31/635—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide having a heterocyclic ring, e.g. sulfadiazine
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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Definitions
- Cancer treatments today include surgery, hormone therapy, radiation, chemotherapy, immunotherapy, targeted therapy and combinations thereof. Survival rates vary by cancer type and by the stage at which the cancer is diagnosed. In 2019, roughly 1.8 million people will be diagnosed with cancer, and an estimated 606,880 people will die of cancer in the United States. Thus, there still exists a need for effective cancer treatments.
- SUMMARY [0004] Some embodiments described herein relate to a combination of compounds that can include an effective amount of Compound (A), or a pharmaceutically acceptable salt thereof, and an effective amount of one or more of Compound (B), or a pharmaceutically acceptable salt thereof.
- Some embodiments described herein relate to the use of a combination of compounds for treating a disease or condition, wherein the combination includes an effective amount of Compound (A), or a pharmaceutically acceptable salt thereof, and an effective amount of one or more of Compound (B), or a pharmaceutically acceptable salt thereof.
- the combination includes an effective amount of Compound (A), or a pharmaceutically acceptable salt thereof, and an effective amount of one or more of Compound (B), or a pharmaceutically acceptable salt thereof.
- inventions described herein relate to the use of a combination of compounds in the manufacture of a medicament for treating a disease or condition, wherein the combination includes an effective amount of Compound (A), or a pharmaceutically acceptable salt thereof, and an effective amount of one or more of Compound (B), or a pharmaceutically acceptable salt thereof.
- the disease or condition can be a cancer described herein.
- Figure 1 provides examples of Compound (A).
- Figure 2 provides examples of Compound (B).
- Figure 3 shows inhibition of monotherapy and combination therapy against RS4;11, DMS053, MV4-11 and Toledo cell lines.
- Figure 4 shows inhibition of monotherapy and combination therapy against the MCF-7 cell line.
- Figure 5 shows tumor volume in response to monotherapy and combination therapy in an HL-60 (AML) mouse model.
- DETAILED DESCRIPTION Definitions for Compound (A), and pharmaceutically acceptable salts thereof [0012] Unless defined otherwise, all technical and scientific terms used herein have the same meaning as is commonly understood by one of ordinary skill in the art. All patents, applications, published applications and other publications referenced herein are incorporated by reference in their entirety unless stated otherwise. In the event that there are a plurality of definitions for a term herein, those in this section prevail unless stated otherwise. [0013] Whenever a group is described as being “optionally substituted” that group may be unsubstituted or substituted with one or more of the indicated substituents.
- the substituent(s) may be selected from one or more the indicated substituents. If no substituents are indicated, it is meant that the indicated “optionally substituted” or “substituted” group may be substituted with one or more group(s) individually and independently selected from alkyl, alkenyl, alkynyl, -2- cycloalkyl, cycloalkenyl, aryl, heteroaryl, heterocyclyl, aryl(alkyl), cycloalkyl(alkyl), heteroaryl(alkyl), heterocyclyl(alkyl), hydroxy, alkoxy, acyl, cyano, halogen, thiocarbonyl, O- carbamyl, N-carbamyl, O-thiocarbamyl, N-thiocarbamyl, C-amido, N-amido, S-sulfonamido, N
- C a to C b in which “a” and “b” are integers refer to the number of carbon atoms in a group.
- the indicated group can contain from “a” to “b”, inclusive, carbon atoms.
- a “Ci to C4 alkyl” group refers to all alkyl groups having from 1 to 4 carbons, that is, CH 3 -, CH 3 CH 2 -, CH 3 CH 2 CH 2 -, (CH ) 2 CH-, CH 3 CH 2 CH 2 CH 2 -, CH3CH2CH(CH3)- and (CH3)3C-. If no “a” and “b” are designated, the broadest range described in these definitions is to be assumed.
- R groups are described as being “taken together” the R groups and the atoms they are attached to can form a cycloalkyl, cycloalkenyl, aryl, heteroaryl or heterocycle.
- R a and R b of an NR a R b group are indicated to be “taken together,” it means that they are covalently bonded to one another to form a ring:
- alkyl refers to a fully saturated aliphatic hydrocarbon group.
- the alkyl moiety may be branched or straight chain.
- branched alkyl groups include, but are not limited to, iso-propyl, sec-butyl, t-butyl and the like.
- straight chain alkyl groups include, but are not limited to, methyl, ethyl, n-propyl, n-butyl, n- pentyl, n-hexyl, n-heptyl and the like.
- the alkyl group may have 1 to 30 carbon atoms (whenever it appears herein, a numerical range such as “1 to 30 refers to each integer in the given range; e.g., “1 to 30 carbon atoms” means that the alkyl group may consist of 1 carbon atom, 2 carbon atoms, 3 carbon atoms, etc., up to and including 30 carbon atoms, although the present definition also covers the occurrence of the term “alkyl” where no numerical range is designated).
- the alkyl group may also be a medium size alkyl having 1 to 12 carbon atoms.
- the alkyl group could also be a lower alkyl having 1 to 6 carbon atoms.
- An alkyl group may be substituted or unsubstituted.
- alkylene refers to a bivalent fully saturated straight chain aliphatic hydrocarbon group.
- alkylene groups include, but are not limited to, methylene, ethylene, propylene, butylene, pentylene, hexylene, heptylene and octylene.
- An alkylene group may be represented by , followed by the number of carbon atoms, followed by a . For example, to represent ethylene.
- the alkylene group may have 1 to 30 carbon atoms (whenever it appears herein, a numerical range such as “1 to 30” refers to each integer in the given range; e.g., “1 to 30 carbon atoms” means that the alkyl group may consist of 1 carbon atom, 2 carbon atoms, 3 carbon atoms, etc., up to and including 30 carbon atoms, although the present definition also covers the occurrence of the term “alkylene” where no numerical range is designated).
- the alkylene group may also be a medium size alkyl having 1 to 12 carbon atoms.
- the alkylene group could also be a lower alkyl having 1 to 4 carbon atoms.
- An alkylene group may be substituted or unsubstituted.
- a lower alkylene group can be substituted by replacing one or more hydrogen of the lower alkylene group and/or by substituting both hydrogens on the same carbon with a C 3-6 monocyclic cycloalkyl group (e.g., ).
- alkenyl used herein refers to a monovalent straight or branched chain radical of from two to twenty carbon atoms containing a carbon double bond(s) including, but not limited to, 1-propenyl, 2-propenyl, 2-methyl-1-propenyl, 1-butenyl, 2-butenyl and the like. An alkenyl group may be unsubstituted or substituted.
- alkynyl refers to a monovalent straight or branched chain radical of from two to twenty carbon atoms containing a carbon triple bond(s) including, but not limited to, 1-propynyl, 1-butynyl, 2-butynyl and the like. An alkynyl group may be unsubstituted or substituted.
- cycloalkyl refers to a completely saturated (no double or triple bonds) mono- or multi- cyclic (such as bicyclic) hydrocarbon ring system. When composed of two or more rings, the rings may be joined together in a fused, bridged or spiro fashion.
- the term “fused” refers to two rings which have two atoms and one bond in common.
- the term “bridged cycloalkyl” refers to compounds wherein the cycloalkyl contains a linkage of one or more atoms connecting non-adjacent atoms.
- the term “spiro” refers to two rings which have one atom in common and the two rings are not linked by a bridge. Cycloalkyl groups can contain 3 to 30 atoms in the ring(s), 3 to 20 atoms in the ring(s), 3 to 10 atoms in the ring(s), 3 to 8 atoms in the ring(s) or 3 to 6 atoms in the ring(s).
- a cycloalkyl group may be unsubstituted or substituted.
- mono-cycloalkyl groups include, but are in no way limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl.
- fused cycloalkyl groups are decahydronaphthalenyl, dodecahydro-1H-phenalenyl and tetradecahydroanthracenyl; examples of bridged cycloalkyl groups are bicyclo[1.1.1]pentyl, adamantanyl and norbornanyl; and examples of spiro cycloalkyl groups include spiro[3.3]heptane and spiro[4.5]decane.
- cycloalkenyl refers to a mono- or multi- cyclic (such as bicyclic) hydrocarbon ring system that contains one or more double bonds in at least one ring; although, if there is more than one, the double bonds cannot form a fully delocalized pi-electron system throughout all the rings (otherwise the group would be “aryl,” as defined herein). Cycloalkenyl groups can contain 3 to 10 atoms in the ring(s), 3 to 8 atoms in the ring(s) or 3 to 6 atoms in the ring(s). When composed of two or more rings, the rings may be connected together in a fused, bridged or spiro fashion.
- aryl refers to a carbocyclic (all carbon) monocyclic or multicyclic (such as bicyclic) aromatic ring system (including fused ring systems where two carbocyclic rings share a chemical bond) that has a fully delocalized pi-electron system throughout all the rings.
- the number of carbon atoms in an aryl group can vary.
- the aryl group can be a C6-C14 aryl group, a C6-C10 aryl group or a C6 aryl group.
- aryl groups include, but are not limited to, benzene, naphthalene and azulene.
- An aryl group may be substituted or unsubstituted.
- heteroaryl refers to a monocyclic or multicyclic (such as bicyclic) aromatic ring system (a ring system with fully delocalized pi-electron system) that contain(s) one or more heteroatoms (for example, 1, 2 or 3 heteroatoms), that is, an element other than carbon, including but not limited to, nitrogen, oxygen and sulfur.
- the number of atoms in the ring(s) of a heteroaryl group can vary.
- the heteroaryl group can contain 4 to 14 atoms in the ring(s), 5 to 10 atoms in the ring(s) or 5 to 6 atoms in the ring(s), such as nine carbon atoms and one heteroatom; eight carbon atoms and two heteroatoms; seven carbon atoms and three heteroatoms; eight carbon atoms and one heteroatom; seven carbon atoms and two heteroatoms; six carbon atoms and three heteroatoms; five carbon atoms and four heteroatoms; five carbon atoms and one heteroatom; four carbon atoms and two heteroatoms; three carbon atoms and three heteroatoms; four carbon atoms and one heteroatom; three carbon atoms and two heteroatoms; or two carbon atoms and three heteroatoms.
- heteroaryl includes fused ring systems where two rings, such as at least one aryl ring and at least one heteroaryl ring or at least two heteroaryl rings, share at least one chemical bond.
- heteroaryl rings include, but are not limited to, furan, furazan, thiophene, benzothiophene, phthalazine, pyrrole, oxazole, benzoxazole, 1,2,3-oxadiazole, 1,2,4-oxadiazole, thiazole, 1,2,3- thiadiazole, 1,2,4-thiadiazole, benzothiazole, imidazole, benzimidazole, indole, indazole, pyrazole, benzopyrazole, isoxazole, benzoisoxazole, isothiazole, triazole, benzotriazole, thiadiazole, tetrazole, pyridine, pyridazine, pyrimidine
- heteroaryl group may be substituted or unsubstituted.
- heterocyclyl or “heteroalicyclyl” refers to three-, four-, five- , six-, seven-, eight-, nine-, ten-, up to 18-membered monocyclic, bicyclic and tricyclic ring system wherein carbon atoms together with from 1 to 5 heteroatoms constitute said ring system.
- a heterocycle may optionally contain one or more unsaturated bonds situated in such a way, however, that a fully delocalized pi-electron system does not occur throughout all the rings.
- the heteroatom(s) is an element other than carbon including, but not limited to, oxygen, sulfur and nitrogen.
- a heterocycle may further contain one or more carbonyl or thiocarbonyl functionalities, so as to make the definition include oxo-systems and thio-systems such as lactams, lactones, cyclic imides, cyclic thioimides and cyclic carbamates.
- oxo-systems and thio-systems such as lactams, lactones, cyclic imides, cyclic thioimides and cyclic carbamates.
- the rings When composed of two or more rings, the rings may be joined together in a fused, bridged or spiro fashion.
- the term “fused” refers to two rings which have two atoms and one bond in common.
- bridged heterocyclyl or “bridged heteroalicyclyl” refers to compounds wherein the heterocyclyl or heteroalicyclyl contains a linkage of one or more atoms connecting non-adjacent atoms.
- spiro refers to two rings which have one atom in common and the two rings are not linked by a bridge.
- Heterocyclyl and heteroalicyclyl groups can contain 3 to 30 atoms in the ring(s), 3 to 20 atoms in the ring(s), 3 to 10 atoms in the ring(s), 3 to 8 atoms in the ring(s) or 3 to 6 atoms in the ring(s).
- any nitrogens in a heteroalicyclic may be quaternized.
- Heterocyclyl or heteroalicyclic groups may be unsubstituted or substituted.
- heterocyclyl or “heteroalicyclyl” groups include but are not limited to, 1,3- dioxin, 1,3-dioxane, 1,4-dioxane, 1,2-dioxolane, 1,3-dioxolane, 1,4-dioxolane, 1,3-oxathiane, 1,4-oxathiin, 1,3-oxathiolane, 1,3-dithiole, 1,3-dithiolane, 1,4-oxathiane, tetrahydro-1,4-thiazine, 2H-1,2-oxazine, maleimide, succinimide, barbituric acid, thiobarbituric acid, dioxopiperazine, hydantoin, dihydrouracil, trioxane, hexahydro-1,3,5-triazine, imidazoline, imidazolidine, isoxazoline, isoxazolidine
- spiro heterocyclyl groups examples include 2-azaspiro[3.3]heptane, 2-oxaspiro[3.3]heptane, 2-oxa-6-azaspiro[3.3]heptane, 2,6- diazaspiro[3.3]heptane, 2-oxaspiro[3.4]octane and 2-azaspiro[3.4]octane.
- aralkyl and “aryl(alkyl)” refer to an aryl group connected, as a substituent, via a lower alkylene group. The lower alkylene and aryl group of an aralkyl may be substituted or unsubstituted.
- heteroarylkyl and “heteroaryl(alkyl)” refer to a heteroaryl group connected, as a substituent, via a lower alkylene group.
- the lower alkylene and heteroaryl group of heteroaralkyl may be substituted or unsubstituted.
- heteroalicyclyl(alkyl) and “heterocyclyl(alkyl)” refer to a heterocyclic or a heteroalicyclic group connected, as a substituent, via a lower alkylene group.
- the lower alkylene and heterocyclyl of a (heteroalicyclyl)alkyl may be substituted or unsubstituted.
- hydroxy refers to a –OH group.
- alkoxy refers to the Formula –OR wherein R is an alkyl, an alkenyl, an alkynyl, a cycloalkyl, a cycloalkenyl, aryl, heteroaryl, heterocyclyl, cycloalkyl(alkyl), aryl(alkyl), heteroaryl(alkyl) or heterocyclyl(alkyl) is defined herein.
- R is an alkyl, an alkenyl, an alkynyl, a cycloalkyl, a cycloalkenyl, aryl, heteroaryl, heterocyclyl, cycloalkyl(alkyl), aryl(alkyl), heteroaryl(alkyl) or heterocyclyl(alkyl) is defined herein.
- a non-limiting list of alkoxys are methoxy, ethoxy, n-propoxy, 1-methylethoxy (isopropoxy), n-butoxy, iso-butoxy,
- acyl refers to a hydrogen, alkyl, alkenyl, alkynyl, aryl, heteroaryl, heterocyclyl, aryl(alkyl), heteroaryl(alkyl) and heterocyclyl(alkyl) connected, as substituents, via a carbonyl group. Examples include formyl, acetyl, propanoyl, benzoyl and acryl. An acyl may be substituted or unsubstituted.
- a “cyano” group refers to a “-CN” group.
- halogen atom or “halogen” as used herein, means any one of the radio-stable atoms of column 7 of the Periodic Table of the Elements, such as, fluorine, chlorine, bromine and iodine.
- An O-carbamyl may be substituted or unsubstituted.
- An N-carbamyl may be substituted or unsubstituted.
- An O-thiocarbamyl may be substituted or unsubstituted.
- An N-thiocarbamyl may be substituted or unsubstituted.
- a C-amido may be substituted or unsubstituted.
- R and RA can be independently hydrogen, an alkyl, an alkenyl, an alkynyl, a cycloalkyl, a cycloalkenyl, aryl, heteroaryl, heterocyclyl, cycloalkyl(alkyl), aryl(alkyl), heteroaryl(alkyl) or heterocyclyl(alkyl).
- An N-amido may be substituted or unsubstituted.
- S-sulfonamido refers to a “-SO2N(RARB)” group in which RA and R B can be independently hydrogen, an alkyl, an alkenyl, an alkynyl, a cycloalkyl, a cycloalkenyl, aryl, heteroaryl, heterocyclyl, cycloalkyl(alkyl), aryl(alkyl), heteroaryl(alkyl) or heterocyclyl(alkyl).
- An S-sulfonamido may be substituted or unsubstituted.
- N-sulfonamido refers to a “RSO2N(RA)-” group in which R and R A can be independently hydrogen, an alkyl, an alkenyl, an alkynyl, a cycloalkyl, a cycloalkenyl, aryl, heteroaryl, heterocyclyl, cycloalkyl(alkyl), aryl(alkyl), heteroaryl(alkyl) or heterocyclyl(alkyl).
- R and R A can be independently hydrogen, an alkyl, an alkenyl, an alkynyl, a cycloalkyl, a cycloalkenyl, aryl, heteroaryl, heterocyclyl, cycloalkyl(alkyl), aryl(alkyl), heteroaryl(alkyl) or heterocyclyl(alkyl).
- An N-sulfonamido may be substituted or unsubstituted.
- An O-carboxy may be substituted or unsubstituted.
- a “sulfenyl” group refers to an “-SR” group in which R can be hydrogen, an alkyl, an alkenyl, an alkynyl, a cycloalkyl, a cycloalkenyl, aryl, heteroaryl, heterocyclyl, cycloalkyl(alkyl), aryl(alkyl), heteroaryl(alkyl) or heterocyclyl(alkyl).
- a sulfenyl may be substituted or unsubstituted.
- a sulfinyl may be substituted or unsubstituted.
- a “sulfonyl” group refers to an “SO 2 R” group in which R can be the same as defined with respect to sulfenyl.
- a sulfonyl may be substituted or unsubstituted.
- haloalkyl refers to an alkyl group in which one or more of the hydrogen atoms are replaced by a halogen (e.g., mono-haloalkyl, di-haloalkyl, tri-haloalkyl and polyhaloalkyl).
- haloalkyl may be substituted or unsubstituted.
- haloalkoxy refers to an alkoxy group in which one or more of the hydrogen atoms are replaced by a halogen (e.g., mono-haloalkoxy, di- haloalkoxy and tri- haloalkoxy).
- Such groups include but are not limited to, chloromethoxy, fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1-chloro-2-fluoromethoxy and 2-fluoroisobutoxy.
- a haloalkoxy may be substituted or unsubstituted.
- a “mono-substituted amine” group refers to a “-NHRA” group in which RA can be an alkyl, an alkenyl, an alkynyl, a cycloalkyl, a cycloalkenyl, aryl, heteroaryl, heterocyclyl, cycloalkyl(alkyl), aryl(alkyl), heteroaryl(alkyl) or heterocyclyl(alkyl), as defined herein.
- the RA may be substituted or unsubstituted.
- a mono-substituted amine group can include, for example, a mono-alkylamine group, a mono-C1-C6 alkylamine group, a mono- arylamine group, a mono-C 6 -C 10 arylamine group and the like.
- Examples of mono-substituted amine groups include, but are not limited to, ⁇ NH(methyl), ⁇ NH(phenyl) and the like.
- a “di-substituted amine” group refers to a “-NRARB” group in which RA and RB can be independently an alkyl, an alkenyl, an alkynyl, a cycloalkyl, a cycloalkenyl, aryl, heteroaryl, heterocyclyl, cycloalkyl(alkyl), aryl(alkyl), heteroaryl(alkyl) or heterocyclyl(alkyl), as defined herein.
- RA and RB can independently be substituted or unsubstituted.
- a di-substituted amine group can include, for example, a di-alkylamine group, a di-C1-C6 alkylamine group, a di- arylamine group, a di-C 6 -C 10 arylamine group and the like.
- Examples of di-substituted amine groups include, but are not limited to, ⁇ N(methyl)2, ⁇ N(phenyl)(methyl), ⁇ N(ethyl)(methyl) and the like.
- “mono-substituted amine(alkyl)” group refers to a mono-substituted amine as provided herein connected, as a substituent, via a lower alkylene group.
- a mono-substituted amine(alkyl) may be substituted or unsubstituted.
- a mono-substituted amine(alkyl) group can include, for example, a mono-alkylamine(alkyl) group, a mono-C1-C6 alkylamine(C1-C6 alkyl) group, a mono-arylamine(alkyl group), a mono-C6-C10 arylamine(C1-C6 alkyl) group and the like.
- Examples of mono-substituted amine(alkyl) groups include, but are not limited to, ⁇ CH2NH(methyl), ⁇ CH2NH(phenyl), ⁇ CH2CH2NH(methyl), ⁇ CH2CH2NH(phenyl) and the like.
- di-substituted amine(alkyl) refers to a di-substituted amine as provided herein connected, as a substituent, via a lower alkylene group.
- a di-substituted amine(alkyl) may be substituted or unsubstituted.
- a di-substituted amine(alkyl) group can include, for example, a dialkylamine(alkyl) group, a di-C 1 -C 6 alkylamine(C 1 -C 6 alkyl) group, a di-arylamine(alkyl) group, a di-C 6 -C 10 arylamine(C 1 -C 6 alkyl) group and the like.
- di-substituted amine(alkyl)groups include, but are not limited to, ⁇ CH2N(methyl)2, ⁇ CH2N(phenyl)(methyl), ⁇ NCH2(ethyl)(methyl), ⁇ CH2CH2N(methyl)2, ⁇ CH 2 CH 2 N(phenyl)(methyl), ⁇ NCH 2 CH 2 (ethyl)(methyl) and the like.
- substituents e.g. haloalkyl
- substituents there may be one or more substituents present.
- “haloalkyl” may include one or more of the same or different halogens.
- C 1 -C 3 alkoxyphenyl may include one or more of the same or different alkoxy groups containing one, two or three atoms.
- a radical indicates species with a single, unpaired electron such that the species containing the radical can be covalently bonded to another species.
- a radical is not necessarily a free radical. Rather, a radical indicates a specific portion of a larger molecule.
- the term “radical” can be used interchangeably with the term “group.”
- pharmaceutically acceptable salt refers to a salt of a compound that does not cause significant irritation to an organism to which it is administered and does not abrogate the biological activity and properties of the compound.
- the salt is an acid addition salt of the compound.
- Pharmaceutical salts can be obtained by reacting a compound with inorganic acids such as hydrohalic acid (e.g., hydrochloric acid or hydrobromic acid), a sulfuric acid, a nitric acid and a phosphoric acid (such as 2,3-dihydroxypropyl dihydrogen phosphate).
- hydrohalic acid e.g., hydrochloric acid or hydrobromic acid
- sulfuric acid e.g., a sulfuric acid, a nitric acid and a phosphoric acid (such as 2,3-dihydroxypropyl dihydrogen phosphate).
- Pharmaceutical salts can also be obtained by reacting a compound with an organic acid such as aliphatic or aromatic carboxylic or sulfonic acids, for example formic, acetic, succinic, lactic, malic, tartaric, citric, ascorbic, nicotinic, methanesulfonic, ethanesulfonic, p-toluensulfonic, trifluoroacetic, benzoic, salicylic, 2-oxopentanedioic or naphthalenesulfonic acid.
- an organic acid such as aliphatic or aromatic carboxylic or sulfonic acids
- Pharmaceutical salts can also be obtained by reacting a compound with a base to form a salt such as an ammonium salt, an alkali metal salt, such as a sodium, a potassium or a lithium salt, an alkaline earth metal salt, such as a calcium or a magnesium salt, a salt of a carbonate, a salt of a bicarbonate, a salt of organic bases such as dicyclohexylamine, N-methyl-D-glucamine, tris(hydroxymethyl)methylamine, C 1 -C 7 alkylamine, cyclohexylamine, triethanolamine, ethylenediamine and salts with amino acids such as arginine and lysine.
- a salt such as an ammonium salt, an alkali metal salt, such as a sodium, a potassium or a lithium salt, an alkaline earth metal salt, such as a calcium or a magnesium salt, a salt of a carbonate, a salt of a bicarbonate, a salt of organic bases such as
- each center may independently be of R-configuration or S-configuration or a mixture thereof.
- the compounds provided herein may be enantiomerically pure, enantiomerically enriched, racemic mixture, diastereomerically pure, diastereomerically enriched or a stereoisomeric mixture.
- each double bond may independently be E or Z a mixture thereof.
- all tautomeric forms are also intended to be included.
- valencies are to be filled with hydrogens or isotopes thereof, e.g., hydrogen-1 (protium) and hydrogen-2 (deuterium).
- hydrogens or isotopes thereof e.g., hydrogen-1 (protium) and hydrogen-2 (deuterium).
- the compounds described herein can be labeled isotopically. Substitution with isotopes such as deuterium may afford certain therapeutic advantages resulting from greater metabolic stability, such as, for example, increased in vivo half-life or reduced dosage requirements.
- Each chemical element as represented in a compound structure may include any isotope of said element.
- a hydrogen atom may be explicitly disclosed or understood to be present in the compound.
- the hydrogen atom can be any isotope of hydrogen, including but not limited to hydrogen-1 (protium) and hydrogen-2 (deuterium).
- reference herein to a compound encompasses all potential isotopic forms unless the context clearly dictates otherwise.
- the methods and combinations described herein include crystalline forms (also known as polymorphs, which include the different crystal packing arrangements of the same elemental composition of a compound), amorphous phases, salts, solvates and hydrates.
- the compounds described herein exist in solvated forms with pharmaceutically acceptable solvents such as water, ethanol or the like. In other embodiments, the compounds described herein exist in unsolvated form.
- Solvates contain either stoichiometric or non-stoichiometric amounts of a solvent, and may be formed during the process of crystallization with pharmaceutically acceptable solvents such as water, ethanol or the like. Hydrates are formed when the solvent is water or alcoholates are formed when the solvent is alcohol.
- the compounds provided herein can exist in unsolvated as well as solvated forms. In general, the solvated forms are considered equivalent to the unsolvated forms for the purposes of the compounds and methods provided herein. [0062] Where a range of values is provided, it is understood that the upper and lower limit, and each intervening value between the upper and lower limit of the range is encompassed within the embodiments.
- the term “comprising” is to be interpreted synonymously with the phrases “having at least” or “including at least”.
- the term “comprising” means that the compound, composition or device includes at least the recited features or components, but may also include additional features or components.
- Compound (A) [0065] Some embodiments disclosed herein relate to the use of a combination of compounds for treating a disease or condition, wherein the combination can include an effective amount of Compound (A), or a pharmaceutically acceptable salt thereof, and an effective amount of one or more of Compound (B), or a pharmaceutically acceptable salt thereof, wherein: the Compound (A) has the structure: wherein: R 1 can be selected from hydrogen, halogen, a substituted or unsubstituted C1-C6 alkyl, a substituted or unsubstituted C1-C6 haloalkyl, a substituted or unsubstituted C3-C6 cycloalkyl, a substituted or unsubstituted C 1 -C 6 alkoxy, an unsubstituted mono-
- R 1 can be halogen, for example, fluoro, chloro, bromo or iodo. In some embodiments, R 1 can be fluoro. In some embodiments, R 1 can be chloro. In some embodiments, R 1 can be hydrogen. [0067] In some embodiments, R 1 can be a substituted or unsubstituted C1-C6 alkyl. For example, in some embodiments, R 1 can be a substituted C 1 -C 6 alkyl. In other embodiments, R 1 can be an unsubstituted C1-C6 alkyl.
- C1-C6 alkyl groups include, but are not limited to methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, pentyl (branched and straight-chained) and hexyl (branched and straight-chained).
- R 1 can be an unsubstituted methyl or an unsubstituted ethyl.
- R 1 can be a substituted or unsubstituted C1-C6 haloalkyl, for example, a substituted or unsubstituted mono-halo C 1 -C 6 alkyl, a substituted or unsubstituted di-halo C 1 -C 6 alkyl, a substituted or unsubstituted tri-halo C 1 -C 6 alkyl, a substituted or unsubstituted tetra-halo C 1 -C 6 alkyl or a substituted or unsubstituted penta-halo C 1 -C 6 alkyl.
- R 1 can be an unsubstituted –CHF2, –CF3, –CH2CF3 or –CF2CH3.
- R 1 can be a substituted or unsubstituted monocyclic or bicyclic C3-C6 cycloalkyl.
- R 1 can be a substituted monocyclic C3-C6 cycloalkyl.
- R 1 can be an unsubstituted monocyclic C3- C 6 cycloalkyl.
- R 1 can be a substituted or unsubstituted C1-C6 alkoxy.
- R 1 can be a substituted C 1 -C 6 alkoxy.
- R 1 can be an unsubstituted C 1 -C 6 alkoxy.
- R 1 can be an unsubstituted methoxy or an unsubstituted ethoxy.
- R 1 can be an unsubstituted mono-C1-C6 alkylamine, for example, methylamine, ethylamine, n-propylamine, isopropylamine, n-butylamine, isobutylamine, tert-butylamine, pentylamine (branched and straight-chained) and hexylamine (branched and straight-chained).
- R 1 can be methylamine or ethylamine.
- R 1 can be an unsubstituted di-C1-C6 alkylamine.
- each C 1 -C 6 alkyl in the di-C 1 -C 6 alkylamine is the same. In other embodiments, each C 1 -C 6 alkyl in the di-C 1 -C 6 alkylamine is different.
- suitable di- C1-C6 alkylamine groups include, but are not limited to di-methylamine, di-ethylamine, (methyl)(ethyl)amine, (methyl)(isopropyl)amine and (ethyl)(isopropyl)amine.
- m can be 0. When m is 0, those skilled in the art understand that the ring to which R 2 is attached is unsubstituted. In some embodiments, m can be 1.
- one R 2 can be an unsubstituted C 1 -C 6 alkyl (for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, pentyl (branched and straight-chained) and hexyl (branched and straight-chained)) and any other R 2 , if present, can be independently selected from halogen (for example, fluoro or chloro), a substituted or unsubstituted C 1 -C 6 alkyl (such as those described herein), a substituted or unsubstituted C 1 -C 6 haloalkyl (such as those described herein) and a substituted or unsubstituted monocyclic or bicyclic C3-C6 cycloalkyl (such as those described herein).
- halogen for example, fluoro or chloro
- each R 2 can be independently selected from an unsubstituted C1-C6 alkyl, such as those described herein.
- m can be 2; and each R 2 can be geminal.
- m can be 2; and each R 2 can be vicinal.
- m can be 2; and each R 2 can be an unsubstituted methyl.
- m can be 2; and each R 2 can be a geminal unsubstituted methyl.
- two R 2 groups can be taken together with the atom(s) to which they are attached to form a substituted or unsubstituted monocyclic C3-C6 cycloalkyl.
- two R 2 groups can be taken together with the atom(s) to which they are attached to form a substituted monocyclic C 3 -C 6 cycloalkyl, such as those described herein.
- two R 2 groups can be taken together with the atom(s) to which they are attached to form an unsubstituted monocyclic C3-C6 cycloalkyl, such as those described herein.
- two R 2 groups can be taken together with the atom to which they are attached to form an unsubstituted cyclopropyl.
- two R 2 groups can be taken together with the atom(s) to which they are attached to form a substituted or unsubstituted monocyclic 3 to 6 membered heterocyclyl.
- two R 2 groups can be taken together with the atom(s) to which they are attached to form a substituted monocyclic 3 to 6 membered heterocyclyl.
- two R 2 groups can be taken together with the atom(s) to which they are attached to form an unsubstituted monocyclic 3 to 6 membered monocyclic heterocyclyl.
- the substituted monocyclic 3 to 6 membered heterocyclyl can be substituted on one or more nitrogen atoms.
- R 4 can be NO 2 .
- R 4 can be cyano.
- R 4 can be halogen.
- R 4 can be an unsubstituted C1-C6 haloalkyl, such as those described herein. In some embodiments, R 4 can be –CF 3 . [0080] In some embodiments, R 4 can be S(O)R 6 . In some embodiments, R 4 can be SO2R 6 . In some embodiments, R 4 can be SO2CF3. [0081] In some embodiments, R 6 can be a substituted or unsubstituted C1-C6 alkyl. For example, in some embodiments, R 6 can be a substituted C 1 -C 6 alkyl, such as those described herein.
- R 6 can be an unsubstituted C1-C6 alkyl, such as those described herein.
- R 6 can be a substituted or unsubstituted monocyclic or bicyclic C3-C6 cycloalkyl.
- R 6 can be a substituted monocyclic or bicyclic C3-C6 cycloalkyl.
- R 6 can be an unsubstituted monocyclic or bicyclic C 3 -C 6 cycloalkyl.
- R 6 can be a substituted or unsubstituted C1-C6 haloalkyl, such as those described herein. In some embodiments, R 6 can be –CF 3 .
- R 5 can be –X 1 -(Alk 1 )n-R 7 . In some embodiments, X 1 can be –O–. In some embodiments, X 1 can be –S–.
- X 1 can be –NH–.
- Alk 1 can be unsubstituted ⁇ (CH2)1-4 ⁇ * for which “*” represents the point of attachment to R 7 .
- Alk 1 can be , , [0086]
- Alk 1 can be a substituted for which “ ” represents the point of attachment to R 7 .
- Alk 1 can be a substituted methylene, a substituted ethylene, a substituted propylene or a substituted butylene.
- Alk 1 can be mono-substituted, di-substituted or tri-substituted.
- Alk 1 can be mono-substituted with a halogen (such as fluoro or chloro) or unsubstituted C 1 -C 3 alkyl, such as those described herein. In other embodiments, Alk 1 can be mono-substituted unsubstituted C 1 -C 3 haloalkyl, such as those described herein. In some embodiments, Alk 1 can be mono-substituted with fluoro or unsubstituted methyl. In some embodiments, Alk 1 can be di-substituted with one fluoro and one unsubstituted C 1 -C 3 alkyl, such as those described herein.
- a halogen such as fluoro or chloro
- Alk 1 can be di-substituted with one unsubstituted C 1 -C 3 haloalkyl, such as those described herein, and one unsubstituted C 1 -C 3 alkyl, such as those described herein. In some embodiments, Alk 1 can be di-substituted with one fluoro and one unsubstituted methyl. In some embodiments, Alk 1 can be di-substituted with two independently selected unsubstituted C 1 -C 3 alkyl groups, such as those described herein. In some embodiments, Alk 1 can be di-substituted with unsubstituted methyl.
- Alk 1 can be selected from: , , , , [0088]
- n can be 0. When n is 0, those skilled in the art understand that X 1 is directly connected to R 7 . In some embodiments, n can be 1.
- R 7 can be a substituted or unsubstituted mono- substituted amine group.
- R 7 can be an amino group mono-substituted with a substituted or unsubstituted C1-C6 alkyl, a substituted or unsubstituted C2-C6 alkenyl, a substituted or unsubstituted C2-C6 alkynyl, a substituted or unsubstituted monocyclic or bicyclic C 3 -C 6 cycloalkyl, a substituted or unsubstituted monocyclic or bicyclic C 6 -C 10 aryl, a substituted or unsubstituted monocyclic or bicyclic 5 to 10 membered heteroaryl, a substituted or unsubstituted monocyclic or bicyclic 3 to 10 membered heterocyclyl, a substituted or unsubstituted monocyclic or bicyclic C 3 -C 6 cycloalkyl(unsubstituted C 1 -C 6 alkyl), a substituted or unsubstituted monocycl
- R 7 can be a substituted or unsubstituted di-substituted amine group.
- R 7 can be an amino group substituted with two substituents independently selected from a substituted or unsubstituted C1-C6 alkyl, a substituted or unsubstituted C 2 -C 6 alkenyl, a substituted or unsubstituted C 2 -C 6 alkynyl, a substituted or unsubstituted monocyclic or bicyclic C3-C6 cycloalkyl, a substituted or unsubstituted monocyclic or bicyclic C6-C10 aryl, a substituted or unsubstituted monocyclic or bicyclic 5 to 10 membered heteroaryl, a substituted or unsubstituted monocyclic or bicyclic 3 to 10 membered heterocyclyl, a substituted or unsubstituted monocyclic or bicyclic C3-C6 cycloalkyl(unsubstituted C1-C6 alkyl), a substituted or unsubstituted
- the two substituents can be the same. In other embodiments the two substituents can be different.
- suitable di-substituted amine groups include, but are not limited to, ⁇ N(methyl) 2 , ⁇ N(ethyl)2, ⁇ N(isopropyl)2, ⁇ N(benzyl)2, ⁇ N(ethyl)(methyl), ⁇ N(isopropyl)(methyl), ⁇ N(ethyl)(isopropyl), ⁇ N(phenyl)(methyl) and ⁇ N(benzyl)(methyl).
- R 7 can be selected from a substituted or unsubstituted N-carbamyl, a substituted or unsubstituted C-amido and a substituted or unsubstituted N-amido.
- R 7 can be a substituted or unsubstituted C3-C10 cycloalkyl.
- R 7 can be a substituted or unsubstituted monocyclic C 3 -C 10 cycloalkyl.
- R 7 can be a substituted or unsubstituted bicyclic C3-C10 cycloalkyl, for example, a bridged, fused or spiro C3-C10 cycloalkyl.
- Suitable substituted or unsubstituted monocyclic or bicyclic C 3 -C 10 cycloalkyl groups include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl, cyclodecyl, spiro[3.3]heptyl, spiro[2.3]hexyl, spiro[3.4]octyl, spiro[3.5]nonyl, spiro[3.6]decyl, spiro[2.4]heptyl, spiro[4.4]nonyl, spiro[4.5]de
- R 7 can be a substituted or unsubstituted C 6 -C 10 spirocycloalkyl. In some embodiments, R 7 can be a substituted C6-C10 spirocycloalkyl. In other embodiments, R 7 can be an unsubstituted C6-C10 spirocycloalkyl.
- R 7 can be a substituted or unsubstituted –cyclopropyl–cyclobutyl spiroalkyl, –cyclopropyl–cyclopentyl spiroalkyl, –cyclopropyl–cyclohexyl spiroalkyl, –cyclopropyl– cycloheptyl spiroalkyl, –cyclopropyl–cyclooctyl spiroalkyl, –cyclobutyl–cyclopropyl spiroalkyl, –cyclobutyl–cyclobutyl spiroalkyl, –cyclobutyl–cyclopentyl spiroalkyl, –cyclobutyl–cyclohexyl spiroalkyl, –cyclobutyl–cycloheptyl spiroalkyl, –cyclopentyl– cyclopropyl spiroalkyl,
- R 7 can be a substituted or unsubstituted 3 to 10 membered heterocyclyl. In some embodiments, R 7 can be a substituted 3 to 10 membered heterocyclyl. In other embodiments, R 7 can be an unsubstituted 3 to 10 membered heterocyclyl. In some embodiments, R 7 can be a substituted or unsubstituted monocyclic 3 to 10 membered heterocyclyl. In other embodiments, R 7 can be a substituted or unsubstituted bicyclic 5 to 10 membered heterocyclyl, for example, a fused, bridged or spiro 5 to 10 membered heterocyclyl.
- Suitable substituted or unsubstituted 3 to 10 membered heterocyclyl groups include, but are not limited to, azidirine, oxirane, azetidine, oxetane, pyrrolidine, tetrahydrofuran, imidazoline, pyrazolidine, piperidine, tetrahydropyran, piperazine, morpholine, thiomorpholine, dioxane, 2- azaspiro[3.3]heptane, 2-oxaspiro[3.3]heptane, 2,6-diazaspiro[3.3]heptane, 2-oxa-6- azaspiro[3.3]heptane, 2-azaspiro[3.4]octane, 6-oxaspiro[3.4]octane, 6-oxa-2-azaspiro[3.4]octane, 7-oxa-2-azaspiro[3.5]nonane, 7-oxaspiro
- the substituted or unsubstituted monocyclic or bicyclic 3 to 10 membered heterocyclyl can be connected to the rest of the molecule through a nitrogen atom. In other embodiments, the substituted or unsubstituted monocyclic or bicyclic 3 to 10 membered heterocyclyl can be connected to the rest of the molecule through a carbon atom. In some embodiments, the substituted monocyclic or bicyclic 3 to 10 membered heterocyclyl can be substituted on one or more nitrogen atoms. [0095] In some embodiments, R 7 can be a substituted or unsubstituted 6 to 10 membered spiro heterocyclyl.
- R 7 can be a substituted 6 to 10 membered spiro heterocyclyl. In other embodiments, R 7 can be an unsubstituted 6 to 10 membered spiro heterocyclyl. In some embodiments, R 7 can be a substituted or unsubstituted azaspirohexane, azaspiroheptane, azaspirooctane, oxaspirohexane, oxaspiroheptane, oxaspirooctane, diazaspirohexane, diazaspiroheptane, diazaspirooctane, dioxaspirohexane, dioxaspiroheptane, dioxaspirooctane, oxa-azaspirohexane, oxa-azaspiroheptane or oxa-azaspirooct
- Suitable substituted or unsubstituted 3 to 10 membered heterocyclyl groups include, but are not limited to, 2-azaspiro[3.3]heptane, 2-oxaspiro[3.3]heptane, 2,6-diazaspiro[3.3]heptane, 2-oxa-6- azaspiro[3.3]heptane, 2-azaspiro[3.4]octane, 6-oxaspiro[3.4]octane, 6-oxa-2-azaspiro[3.4]octane, 7-oxa-2-azaspiro[3.5]nonane, 7-oxaspiro[3.5]nonane and 2-oxa-8-azaspiro[4.5]decane.
- the substituted or unsubstituted 6 to 10 membered spiro heterocyclyl can be connected to the rest of the molecule through a nitrogen atom. In other embodiments, the substituted or unsubstituted 6 to 10 membered spiro heterocyclyl can be connected to the rest of the molecule through a carbon atom. In some embodiments, the substituted 6 to 10 membered spiroheterocyclyl can be substituted on one or more nitrogen atoms. [0096] In some embodiments, R 7 can be hydroxy or amino. [0097] In some embodiments, R 7 can be unsubstituted. In other embodiments, R 7 can be substituted.
- R 7 can be substituted with 1 or 2 substituents independently selected from an unsubstituted C1-C6 alkyl (such as those described herein), an unsubstituted C1-C6 alkoxy (such as those described herein), fluoro, chloro, hydroxy and -SO2- (unsubstituted C 1 -C 6 alkyl).
- the C 1 -C 6 alkoxy, C 3 -C 10 cycloalkyl, 3 to 10 membered heterocyclyl, mono-substituted amine group, di-substituted amine group, N-carbamyl, C-amido and N-amido groups of R 7 can be substituted with 1 or 2 substituents independently selected from any of the aforementioned substituents. [0098] In some embodiments, R 7 can be , , , o .
- R 7 can be [0100] In some embodiments, R 7 can be For example, in some O embodiments R 7 can be or In some embodiment 7 s R can be For example, in some embodiments R 7 can be or In some embodiments R 7 can be In some embodi 7 ments R can be For example, in some embodiments R 7 can be or 7 . In some embodiments R can be . For exam 7 ple, in some embodiments R can be or , such as or [0101]
- Compound (A), or a pharmaceutically acceptable salt thereof can be selected from a compound of Formula (AA), Formula (BB), Formula (CC) and Formula (DD): or pharmaceutically acceptable salts of any of the foregoing. [0102] A non-limiting list of Bcl-2 inhibitors of Compound (A) are described herein, and include those provided in Figure 1. [0103] Examples of Compound (A) include the following: ,
- Compound (A), along with pharmaceutically acceptable salts thereof, can be prepared as described herein and in WO 2019/139902, WO 2019/139900, WO 2019/139907 and WO 2019/139899, which are each hereby incorporated by reference in their entireties. As described in WO 2019/139902, WO 2019/139900, WO 2019/139907 and WO 2019/139899, Compound (A) is a Bcl-2 inhibitor. Definitions for Compound (B), and pharmaceutically acceptable salts thereof [0105] Unless defined otherwise, all technical and scientific terms used herein have the same meaning as is commonly understood by one of ordinary skill in the art.
- the indicated “optionally substituted” or “substituted” group may be substituted with one or more group(s) individually and independently selected from alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heterocyclyl, aryl(alkyl), cycloalkyl(alkyl), heteroaryl(alkyl), heterocyclyl(alkyl), hydroxy, alkoxy, acyl, cyano, halogen, thiocarbonyl, O- carbamyl, N-carbamyl, O-thiocarbamyl, N-thiocarbamyl, C-amido, N-amido, S-sulfonamido, N-sulfonamido, C-carboxy, O-carboxy, nitro, sulfenyl, sulfinyl, sulfonyl,
- C a to C b in which “a” and “b” are integers refer to the number of carbon atoms in a group.
- the indicated group can contain from “a” to “b”, inclusive, carbon atoms.
- a “C1 to C4 alkyl” group refers to all alkyl groups having from 1 to 4 carbons, that is, CH 3 -, CH 3 CH 2 -, CH 3 CH 2 CH 2 -, (CH 3 ) 2 CH-, CH 3 CH 2 CH 2 CH 2 -, CH3CH2CH(CH3)- and (CH3)3C-. If no “a” and “b” are designated, the broadest range described in these definitions is to be assumed.
- R groups are described as being “taken together” the R groups and the atoms they are attached to can form a cycloalkyl, cycloalkenyl, aryl, heteroaryl or heterocycle.
- R a and R b of an NR a R b group are indicated to be “taken together,” it means that they are covalently bonded to one another to form a ring:
- alkyl refers to a fully saturated aliphatic hydrocarbon group. The alkyl moiety may be branched or straight chain.
- Examples of branched alkyl groups include, but are not limited to, iso-propyl, sec-butyl, t-butyl and the like.
- Examples of straight chain alkyl groups include, but are not limited to, methyl, ethyl, n-propyl, n-butyl, n- pentyl, n-hexyl, n-heptyl and the like.
- the alkyl group may have 1 to 30 carbon atoms (whenever it appears herein, a numerical range such as “1 to 30” refers to each integer in the given range; e.g., “1 to 30 carbon atoms” means that the alkyl group may consist of 1 carbon atom, 2 carbon atoms, 3 carbon atoms, etc., up to and including 30 carbon atoms, although the present definition also covers the occurrence of the term “alkyl” where no numerical range is designated).
- the alkyl group may also be a medium size alkyl having 1 to 12 carbon atoms.
- the alkyl group could also be a lower alkyl having 1 to 6 carbon atoms.
- An alkyl group may be substituted or unsubstituted.
- alkenyl used herein refers to a monovalent straight or branched chain radical of from two to twenty carbon atoms containing a carbon double bond(s) including, but not limited to, 1-propenyl, 2-propenyl, 2-methyl-1-propenyl, 1-butenyl, 2-butenyl and the like. An alkenyl group may be unsubstituted or substituted.
- alkynyl used herein refers to a monovalent straight or branched chain radical of from two to twenty carbon atoms containing a carbon triple bond(s) including, but not limited to, 1-propynyl, 1-butynyl, 2-butynyl and the like.
- alkynyl group may be unsubstituted or substituted.
- cycloalkyl refers to a completely saturated (no double or triple bonds) mono- or multi- cyclic hydrocarbon ring system. When composed of two or more rings, the rings may be joined together in a fused, bridged or spiro fashion.
- fused refers to two rings which have two atoms and one bond in common.
- bridged cycloalkyl refers to compounds wherein the cycloalkyl contains a linkage of one or more atoms connecting non-adjacent atoms.
- Cycloalkyl groups can contain 3 to 30 atoms in the ring(s), 3 to 20 atoms in the ring(s), 3 to 10 atoms in the ring(s), 3 to 8 atoms in the ring(s) or 3 to 6 atoms in the ring(s).
- a cycloalkyl group may be unsubstituted or substituted.
- Examples of mono-cycloalkyl groups include, but are in no way limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl.
- Examples of fused cycloalkyl groups are decahydronaphthalenyl, dodecahydro-1H-phenalenyl and tetradecahydroanthracenyl;
- examples of bridged cycloalkyl groups are bicyclo[1.1.1]pentyl, adamantanyl and norbornanyl; and examples of spiro cycloalkyl groups include spiro[3.3]heptane and spiro[4.5]decane.
- cycloalkenyl refers to a mono- or multi- cyclic hydrocarbon ring system that contains one or more double bonds in at least one ring; although, if there is more than one, the double bonds cannot form a fully delocalized pi-electron system throughout all the rings (otherwise the group would be “aryl,” as defined herein). Cycloalkenyl groups can contain 3 to 10 atoms in the ring(s), 3 to 8 atoms in the ring(s) or 3 to 6 atoms in the ring(s). When composed of two or more rings, the rings may be connected together in a fused, bridged or spiro fashion.
- a cycloalkenyl group may be unsubstituted or substituted.
- “carbocyclyl” refers to a non-aromatic a mono- or multi- cyclic hydrocarbon ring system. When composed of two or more rings, the rings may be joined together in a fused, bridged or spiro fashion, as described herein. Carbocyclyl groups can contain 3 to 30 atoms in the ring(s), 3 to 20 atoms in the ring(s), 3 to 10 atoms in the ring(s), 3 to 8 atoms in the ring(s) or 3 to 6 atoms in the ring(s). A carbocyclyl group may be unsubstituted or substituted.
- carbocyclyl groups include, but are in no way limited to, cycloalkyl groups and cycloalkenyl groups, as defined herein, and the non-aromatic portions of 1,2,3,4- tetrahydronaphthalene, 2,3-dihydro-1H-indene, 5,6,7,8-tetrahydroquinoline and 6,7-dihydro-5H- cyclopenta[b]pyridine.
- aryl refers to a carbocyclic (all carbon) monocyclic or multicyclic aromatic ring system (including fused ring systems where two carbocyclic rings share a chemical bond) that has a fully delocalized pi-electron system throughout all the rings.
- the number of carbon atoms in an aryl group can vary.
- the aryl group can be a C6- C14 aryl group, a C6-C10 aryl group or a C6 aryl group.
- Examples of aryl groups include, but are not limited to, benzene, naphthalene and azulene.
- An aryl group may be substituted or unsubstituted.
- heteroaryl refers to a monocyclic or multicyclic aromatic ring system (a ring system with fully delocalized pi-electron system) that contain(s) one or more heteroatoms (for example, 1, 2 or 3 heteroatoms), that is, an element other than carbon, including but not limited to, nitrogen, oxygen and sulfur.
- heteroatoms for example, 1, 2 or 3 heteroatoms
- the number of atoms in the ring(s) of a heteroaryl group can vary.
- the heteroaryl group can contain 4 to 14 atoms in the ring(s), 5 to 10 atoms in the ring(s) or 5 to 6 atoms in the ring(s), such as nine carbon atoms and one heteroatom; eight carbon atoms and two heteroatoms; seven carbon atoms and three heteroatoms; eight carbon atoms and one heteroatom; seven carbon atoms and two heteroatoms; six carbon atoms and three heteroatoms; five carbon atoms and four heteroatoms; five carbon atoms and one heteroatom; four carbon atoms and two heteroatoms; three carbon atoms and three heteroatoms; four carbon atoms and one heteroatom; three carbon atoms and two heteroatoms; or two carbon atoms and three heteroatoms.
- heteroaryl includes fused ring systems where two rings, such as at least one aryl ring and at least one heteroaryl ring or at least two heteroaryl rings, share at least one chemical bond.
- heteroaryl rings include, but are not limited to, furan, furazan, thiophene, benzothiophene, phthalazine, pyrrole, oxazole, benzoxazole, 1,2,3-oxadiazole, 1,2,4-oxadiazole, thiazole, 1,2,3-thiadiazole, 1,2,4-thiadiazole, benzothiazole, imidazole, benzimidazole, indole, indazole, pyrazole, benzopyrazole, isoxazole, benzoisoxazole, isothiazole, triazole, benzotriazole, thiadiazole, tetrazole, pyridine, pyridazine, pyrimidine,
- heteroaryl group may be substituted or unsubstituted.
- heterocyclyl or “heteroalicyclyl” refers to three-, four-, five- , six-, seven-, eight-, nine-, ten-, up to 18-membered monocyclic, bicyclic and tricyclic ring system wherein carbon atoms together with from 1 to 5 heteroatoms constitute said ring system.
- a heterocycle may optionally contain one or more unsaturated bonds situated in such a way, however, that a fully delocalized pi-electron system does not occur throughout all the rings.
- the heteroatom(s) is an element other than carbon including, but not limited to, oxygen, sulfur and nitrogen.
- a heterocycle may further contain one or more carbonyl or thiocarbonyl functionalities, so as to make the definition include oxo-systems and thio-systems such as lactams, lactones, cyclic imides, cyclic thioimides and cyclic carbamates.
- oxo-systems and thio-systems such as lactams, lactones, cyclic imides, cyclic thioimides and cyclic carbamates.
- the rings When composed of two or more rings, the rings may be joined together in a fused, bridged or spiro fashion.
- the term “fused” refers to two rings which have two atoms and one bond in common.
- bridged heterocyclyl or “bridged heteroalicyclyl” refers to compounds wherein the heterocyclyl or heteroalicyclyl contains a linkage of one or more atoms connecting non-adjacent atoms.
- spiro refers to two rings which have one atom in common and the two rings are not linked by a bridge.
- Heterocyclyl and heteroalicyclyl groups can contain 3 to 30 atoms in the ring(s), 3 to 20 atoms in the ring(s), 3 to 10 atoms in the ring(s), 3 to 8 atoms in the ring(s) or 3 to 6 atoms in the ring(s).
- any nitrogens in a heteroalicyclic may be quaternized.
- Heterocyclyl or heteroalicyclic groups may be unsubstituted or substituted.
- heterocyclyl or “heteroalicyclyl” groups include but are not limited to, 1,3- dioxin, 1,3-dioxane, 1,4-dioxane, 1,2-dioxolane, 1,3-dioxolane, 1,4-dioxolane, 1,3-oxathiane, 1,4-oxathiin, 1,3-oxathiolane, 1,3-dithiole, 1,3-dithiolane, 1,4-oxathiane, tetrahydro-1,4-thiazine, 2H-1,2-oxazine, maleimide, succinimide, barbituric acid, thiobarbituric acid, dioxopiperazine, hydantoin, dihydrouracil, trioxane, hexahydro-1,3,5-triazine, imidazoline, imidazolidine, isoxazoline, isoxazolidine
- spiro heterocyclyl groups examples include 2-azaspiro[3.3]heptane, 2-oxaspiro[3.3]heptane, 2-oxa-6-azaspiro[3.3]heptane, 2,6- diazaspiro[3.3]heptane, 2-oxaspiro[3.4]octane and 2-azaspiro[3.4]octane.
- aralkyl and “aryl(alkyl)” refer to an aryl group connected, as a substituent, via a lower alkylene group. The lower alkylene and aryl group of an aralkyl may be substituted or unsubstituted.
- heteroarylkyl and “heteroaryl(alkyl)” refer to a heteroaryl group connected, as a substituent, via a lower alkylene group.
- the lower alkylene and heteroaryl group of heteroaralkyl may be substituted or unsubstituted.
- heteroalicyclyl(alkyl) and “heterocyclyl(alkyl)” refer to a heterocyclic or a heteroalicyclic group connected, as a substituent, via a lower alkylene group.
- the lower alkylene and heterocyclyl of a (heteroalicyclyl)alkyl may be substituted or unsubstituted.
- lower alkylene groups are straight-chained -CH2- tethering groups, forming bonds to connect molecular fragments via their terminal carbon atoms. Examples include but are not limited to methylene (-CH 2 -), ethylene (-CH 2 CH 2 -), propylene (- CH2CH2CH2-) and butylene (-CH2CH2CH2CH2-).
- a lower alkylene group can be substituted by replacing one or more hydrogen of the lower alkylene group and/or by substituting both hydrogens on the same carbon with a cycloalkyl group (e.g., ).
- a cycloalkyl group e.g., .
- alkoxy refers to the Formula –OR wherein R is an alkyl, an alkenyl, an alkynyl, a cycloalkyl, a cycloalkenyl, aryl, heteroaryl, heterocyclyl, cycloalkyl(alkyl), aryl(alkyl), heteroaryl(alkyl) or heterocyclyl(alkyl) is defined herein.
- R is an alkyl, an alkenyl, an alkynyl, a cycloalkyl, a cycloalkenyl, aryl, heteroaryl, heterocyclyl, cycloalkyl(alkyl), aryl(alkyl), heteroaryl(alkyl) or heterocyclyl(alkyl) is defined herein.
- a non-limiting list of alkoxys are methoxy, ethoxy, n-propoxy, 1-methylethoxy (iso-propoxy), n-butoxy, iso-butoxy
- acyl refers to a hydrogen, alkyl, alkenyl, alkynyl, aryl, heteroaryl, heterocyclyl, aryl(alkyl), heteroaryl(alkyl) and heterocyclyl(alkyl) connected, as substituents, via a carbonyl group. Examples include formyl, acetyl, propanoyl, benzoyl and acryl. An acyl may be substituted or unsubstituted. [0125] A “cyano” group refers to a “-CN” group.
- halogen atom or “halogen” as used herein, means any one of the radio-stable atoms of column 7 of the Periodic Table of the Elements, such as, fluorine, chlorine, bromine and iodine.
- An O-carbamyl may be substituted or unsubstituted.
- An N-carbamyl may be substituted or unsubstituted.
- An O-thiocarbamyl may be substituted or unsubstituted.
- An N-thiocarbamyl may be substituted or unsubstituted.
- a C-amido may be substituted or unsubstituted.
- R and R A can be independently hydrogen, an alkyl, an alkenyl, an alkynyl, a cycloalkyl, a cycloalkenyl, aryl, heteroaryl, heterocyclyl, cycloalkyl(alkyl), aryl(alkyl), heteroaryl(alkyl) or heterocyclyl(alkyl).
- An N-amido may be substituted or unsubstituted.
- S-sulfonamido refers to a “-SO2N(RARB)” group in which RA and RB can be independently hydrogen, an alkyl, an alkenyl, an alkynyl, a cycloalkyl, a cycloalkenyl, aryl, heteroaryl, heterocyclyl, cycloalkyl(alkyl), aryl(alkyl), heteroaryl(alkyl) or heterocyclyl(alkyl).
- An S-sulfonamido may be substituted or unsubstituted.
- N-sulfonamido refers to a “RSO2N(RA)-” group in which R and R A can be independently hydrogen, an alkyl, an alkenyl, an alkynyl, a cycloalkyl, a cycloalkenyl, aryl, heteroaryl, heterocyclyl, cycloalkyl(alkyl), aryl(alkyl), heteroaryl(alkyl) or heterocyclyl(alkyl).
- R and R A can be independently hydrogen, an alkyl, an alkenyl, an alkynyl, a cycloalkyl, a cycloalkenyl, aryl, heteroaryl, heterocyclyl, cycloalkyl(alkyl), aryl(alkyl), heteroaryl(alkyl) or heterocyclyl(alkyl).
- An N-sulfonamido may be substituted or unsubstituted.
- An O-carboxy may be substituted or unsubstituted.
- a “nitro” group refers to an “–NO 2 ” group.
- a “sulfenyl” group refers to an “-SR” group in which R can be hydrogen, an alkyl, an alkenyl, an alkynyl, a cycloalkyl, a cycloalkenyl, aryl, heteroaryl, heterocyclyl, cycloalkyl(alkyl), aryl(alkyl), heteroaryl(alkyl) or heterocyclyl(alkyl).
- a sulfenyl may be substituted or unsubstituted.
- a sulfinyl may be substituted or unsubstituted.
- a “sulfonyl” group refers to an “SO 2 R” group in which R can be the same as defined with respect to sulfenyl.
- a sulfonyl may be substituted or unsubstituted.
- haloalkyl refers to an alkyl group in which one or more of the hydrogen atoms are replaced by a halogen (e.g., mono-haloalkyl, di-haloalkyl, tri-haloalkyl and polyhaloalkyl).
- haloalkyl may be substituted or unsubstituted.
- haloalkoxy refers to an alkoxy group in which one or more of the hydrogen atoms are replaced by a halogen (e.g., mono-haloalkoxy, di- haloalkoxy and tri- haloalkoxy).
- Such groups include but are not limited to, chloromethoxy, fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1-chloro-2-fluoromethoxy and 2-fluoroisobutoxy.
- a haloalkoxy may be substituted or unsubstituted.
- a “mono-substituted amine” group refers to a “-NHRA” group in which RA can be an alkyl, an alkenyl, an alkynyl, a cycloalkyl, a cycloalkenyl, aryl, heteroaryl, heterocyclyl, cycloalkyl(alkyl), aryl(alkyl), heteroaryl(alkyl) or heterocyclyl(alkyl), as defined herein.
- the RA may be substituted or unsubstituted. Examples of mono-substituted amino groups include, but are not limited to, ⁇ NH(methyl), ⁇ NH(phenyl) and the like.
- a “di-substituted amine” group refers to a “-NR A R B ” group in which R A and RB can be independently an alkyl, an alkenyl, an alkynyl, a cycloalkyl, a cycloalkenyl, aryl, heteroaryl, heterocyclyl, cycloalkyl(alkyl), aryl(alkyl), heteroaryl(alkyl) or heterocyclyl(alkyl), as defined herein.
- R A and R B can independently be substituted or unsubstituted.
- amine(alkyl) refers to an -(alkylene)-NR’R” radical where R’ and R” are independently hydrogen or alkyl as defined herein.
- An amine(alkyl) may be substituted or unsubstituted.
- Examples of amine(alkyl) groups include, but are not limited to, ⁇ CH2NH(methyl), ⁇ CH2NH(phenyl), ⁇ CH2CH2NH(methyl), ⁇ CH2CH2NH(phenyl), ⁇ CH 2 N(methyl) 2 , ⁇ CH 2 N(phenyl)(methyl), ⁇ NCH 2 (ethyl)(methyl), ⁇ CH 2 CH 2 N(methyl) 2 , ⁇ CH2CH2N(phenyl)(methyl), ⁇ NCH2CH2(ethyl)(methyl) and the like. [0148] Where the number of substituents is not specified (e.g. haloalkyl), there may be one or more substituents present.
- haloalkyl may include one or more of the same or different halogens.
- C1-C3 alkoxyphenyl may include one or more of the same or different alkoxy groups containing one, two or three atoms.
- a radical indicates species with a single, unpaired electron such that the species containing the radical can be covalently bonded to another species.
- a radical is not necessarily a free radical. Rather, a radical indicates a specific portion of a larger molecule.
- the term “radical” can be used interchangeably with the term “group.”
- pharmaceutically acceptable salt refers to a salt of a compound that does not cause significant irritation to an organism to which it is administered and does not abrogate the biological activity and properties of the compound.
- the salt is an acid addition salt of the compound.
- Pharmaceutical salts can be obtained by reacting a compound with inorganic acids such as hydrohalic acid (e.g., hydrochloric acid or hydrobromic acid), a sulfuric acid, a nitric acid and a phosphoric acid (such as 2,3-dihydroxypropyl dihydrogen phosphate).
- Pharmaceutical salts can also be obtained by reacting a compound with an organic acid such as aliphatic or aromatic carboxylic or sulfonic acids, for example formic, acetic, succinic, lactic, malic, tartaric, citric, ascorbic, nicotinic, methanesulfonic, ethanesulfonic, p-toluenesulfonic, trifluoroacetic, benzoic, salicylic, 2-oxopentanedioic or naphthalenesulfonic acid.
- an organic acid such as aliphatic or aromatic carboxylic or sulfonic acids
- Pharmaceutical salts can also be obtained by reacting a compound with a base to form a salt such as an ammonium salt, an alkali metal salt, such as a sodium, a potassium or a lithium salt, an alkaline earth metal salt, such as a calcium or a magnesium salt, a salt of a carbonate, a salt of a bicarbonate, a salt of organic bases such as dicyclohexylamine, N-methyl-D-glucamine, tris(hydroxymethyl)methylamine, C1-C7 alkylamine, cyclohexylamine, triethanolamine, ethylenediamine and salts with amino acids such as arginine and lysine.
- a salt such as an ammonium salt, an alkali metal salt, such as a sodium, a potassium or a lithium salt, an alkaline earth metal salt, such as a calcium or a magnesium salt, a salt of a carbonate, a salt of a bicarbonate, a salt of organic bases such as di
- each center may independently be of R-configuration or S-configuration or a mixture thereof.
- the compounds provided herein may be enantiomerically pure, enantiomerically enriched, racemic mixture, diastereomerically pure, diastereomerically enriched or a stereoisomeric mixture.
- each double bond may independently be E or Z a mixture thereof.
- all tautomeric forms are also intended to be included.
- valencies are to be filled with hydrogens or isotopes thereof, e.g., hydrogen-1 (protium) and hydrogen-2 (deuterium).
- hydrogens or isotopes thereof e.g., hydrogen-1 (protium) and hydrogen-2 (deuterium).
- the compounds described herein can be labeled isotopically. Substitution with isotopes such as deuterium may afford certain therapeutic advantages resulting from greater metabolic stability, such as, for example, increased in vivo half-life or reduced dosage requirements.
- Each chemical element as represented in a compound structure may include any isotope of said element.
- a hydrogen atom may be explicitly disclosed or understood to be present in the compound.
- the hydrogen atom can be any isotope of hydrogen, including but not limited to hydrogen-1 (protium) and hydrogen-2 (deuterium).
- reference herein to a compound encompasses all potential isotopic forms unless the context clearly dictates otherwise.
- the methods and combinations described herein include crystalline forms (also known as polymorphs, which include the different crystal packing arrangements of the same elemental composition of a compound), amorphous phases, salts, solvates and hydrates.
- the compounds described herein exist in solvated forms with pharmaceutically acceptable solvents such as water, ethanol or the like. In other embodiments, the compounds described herein exist in unsolvated form.
- Solvates contain either stoichiometric or non-stoichiometric amounts of a solvent, and may be formed during the process of crystallization with pharmaceutically acceptable solvents such as water, ethanol or the like. Hydrates are formed when the solvent is water or alcoholates are formed when the solvent is alcohol.
- the compounds provided herein can exist in unsolvated as well as solvated forms. In general, the solvated forms are considered equivalent to the unsolvated forms for the purposes of the compounds and methods provided herein. [0155] Where a range of values is provided, it is understood that the upper and lower limit, and each intervening value between the upper and lower limit of the range is encompassed within the embodiments.
- the term “comprising” is to be interpreted synonymously with the phrases “having at least” or “including at least”.
- the term “comprising” means that the compound, composition or device includes at least the recited features or components, but may also include additional features or components.
- Compound (B) [0158] As described herein, some embodiments disclosed herein relate to the use of a combination of compounds for treating a disease or condition, wherein the combination can include an effective amount of Compound (A), or a pharmaceutically acceptable salt thereof (as described herein), and an effective amount of one or more of Compound (B), or a pharmaceutically acceptable salt thereof, wherein: the Compound (B) has the structure: wherein: R 1a can be selected from hydrogen, halogen and a substituted or unsubstituted C1-C6 alkyl; Ring A-a can be selected from a substituted or unsubstituted phenyl and a substituted or unsubstituted 5-6 membered monocyclic heteroaryl; Ring B-a can be selected from a substituted or unsubstit
- R 1a can be selected from hydrogen, halogen and a substituted or unsubstituted C 1 -C 6 alkyl.
- Ring A-a can be selected from a substituted or unsubstituted phenyl and a substituted or unsubstituted 5-6 membered monocyclic heteroaryl.
- Ring B-a can be selected from a substituted or unsubstituted monocyclic 5-7 membered carbocyclyl and a substituted or unsubstituted 5-7 membered monocyclic heterocyclyl.
- R 2a can be selected from and .
- m-a can be 0, 1, 2 or 3.
- R 3a can be selected from halogen and a substituted or unsubstituted C1-C6 alkyl.
- X-a can be selected from hydrogen, halogen, hydroxy, cyano, a substituted or unsubstituted 4-6 membered monocyclic heterocyclyl, a substituted or unsubstituted amine(C 1 -C 6 alkyl), a substituted or unsubstituted –NH-(CH2)1-6-amine, a mono-substituted amine, a di-substituted amine, an amino, a substituted or unsubstituted C1-C6 alkyl, a substituted or unsubstituted C1-C6 alkoxy, a substituted or unsubstituted C 3 -C 6 cycloalkoxy, a substituted or unsubstituted (C 1 -C 6 alkyl)acyl, a substituted or unsubstituted (C 1
- Y-a can be CH or N.
- Y 1-a can be CR 4A-a or N.
- Y 2- a can be CR 4B-a or N.
- Ring C-a can be selected from a substituted or unsubstituted C6-C10 aryl, a substituted or unsubstituted monocyclic 5-10 membered heteroaryl, a substituted or unsubstituted monocyclic 5-7 membered carbocyclyl, a substituted or unsubstituted 5-7 membered monocyclic heterocyclyl and a substituted or unsubstituted 7-10 membered bicyclic heterocyclyl.
- R 4A-a and R 4B-a are independently selected from hydrogen, halogen and an unsubstituted C 1-4 alkyl.
- R 1a can be selected from hydrogen, halogen and C1-C6 alkyl.
- R 1a can be hydrogen.
- R 1a can be halogen.
- R 1a can be fluoro.
- R 1a can be an unsubstituted C1-C6 alkyl (such as methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, t-butyl, pentyl (straight chain or branched) or hexyl (straight chain or branched)).
- R 1a can be an unsubstituted methyl.
- R 1a can be a substituted C 1 -C 6 alkyl, such as those described herein.
- R 1a can be an unsubstituted C1-C6 haloalkyl (such as a C1-C6 fluoroalkyl, a C1-C6 chloroalkyl or a C1-C6 chlorofluoroalkyl).
- R 1a can be –CHF 2 , –CF 3 , –CF 2 CH 3 or –CH 2 CF 3 .
- Ring A-a can be selected from a substituted or unsubstituted phenyl and a substituted or unsubstituted 5-6 membered monocyclic heteroaryl.
- Ring A-a can be a substituted phenyl. In other embodiments, Ring A can be an unsubstituted phenyl. [0163] In some embodiments, Ring A-a can be a substituted 5-6 membered monocyclic heteroaryl. In some embodiments, Ring A-a can be an unsubstituted 5-6 membered monocyclic heteroaryl.
- Ring A-a can be selected from a substituted or unsubstituted pyrrole, a substituted or unsubstituted furan, a substituted or unsubstituted thiophene, a substituted or unsubstituted imidazole, a substituted or unsubstituted pyrazole, a substituted or unsubstituted oxazole, a substituted or unsubstituted thiazole, a substituted or unsubstituted pyridine, a substituted or unsubstituted pyrazine, a substituted or unsubstituted pyrimidine and a substituted or unsubstituted pyridazine.
- Ring A-a When substituted, Ring A-a can be substituted with one or more substituents selected from halogen, an unsubstituted C 1 -C 4 haloalkyl and an unsubstituted C 1 -C 4 alkyl. In some embodiments, Ring A-a is mono-substituted with a halogen (for example, fluoro). [0165] In some embodiments, can be selected from:
- each of the aforementioned groups are substituted or unsubstituted.
- Ring B-a can be selected from a substituted or unsubstituted monocyclic 5-7 membered carbocyclyl and a substituted or unsubstituted 5-7 membered monocyclic heterocyclyl.
- Ring B-a can be a substituted or unsubstituted monocyclic 5-7 membered carbocyclyl.
- Ring B-a can be a substituted or unsubstituted monocyclic 5 membered carbocyclyl.
- Ring B-a can be a substituted or unsubstituted monocyclic 6 membered carbocyclyl.
- Ring B-a can be a substituted or unsubstituted monocyclic 7 membered carbocyclyl. [0168] In some embodiments, can be selected from an ; wherein each of the aforementioned groups are substituted or unsubstituted. 169] In some embodiments, Ring B-a can be a substituted or unsubstituted monocyclic 5-7 membered heterocyclyl. In some embodiments, Ring B-a can be a substituted or unsubstituted monocyclic 5 membered heterocyclyl. In other embodiments, Ring B-a can be a substituted or unsubstituted monocyclic 6 membered heterocyclyl.
- Ring B-a can be a substituted or unsubstituted monocyclic 7 membered heterocyclyl. [0170] In some embodiments, can be selected from , , A and ; wherein each of the aforementioned groups uding H group.
- Ring B-a can be selected from and , wherein each of the aforementioned groups are substituted or unsubstituted, including any –NH group. In some embodiments, Ring B-a can be a substituted or unsubstituted .
- Ring B-a when Ring B-a is substituted, Ring B-a can be substituted with 1, 2 or 3 substituents independently selected from halogen, hydroxy, amino, an unsubstituted N-linked amido (for example, –NHC(O)C 1- C 6 alkyl), an unsubstituted C 1 -C 6 haloalkyl (such as those described herein) and a substituted or unsubstituted C1-C6 alkyl (such as those described herein).
- substituents independently selected from halogen, hydroxy, amino, an unsubstituted N-linked amido (for example, –NHC(O)C 1- C 6 alkyl), an unsubstituted C 1 -C 6 haloalkyl (such as those described herein) and a substituted or unsubstituted C1-C6 alkyl (such as those described herein).
- Ring B-a when Ring B-a is substituted, Ring B-a can be substituted with 1, 2 or 3 substituents independently selected from halogen, hydroxy, amino, an unsubstituted N-linked amido (for example, –NHC(O)C1-C6 alkyl) and a substituted or unsubstituted C1-C6 alkyl (such as those described herein).
- substituents independently selected from halogen, hydroxy, amino, an unsubstituted N-linked amido (for example, –NHC(O)C1-C6 alkyl) and a substituted or unsubstituted C1-C6 alkyl (such as those described herein).
- Ring B-a can be substituted with 1, 2 or 3 substituents independently selected from fluoro, hydroxy, amino, an unsubstituted –NHC(O)C 1- C 6 alkyl, an unsubstituted C 1 -C 6 haloalkyl (such as those described herein) and an unsubstituted C1-C6 alkyl (such as those described herein).
- Ring B-a can be substituted with 1 or 2 substituents independently selected from fluoro, hydroxy, –CF 3 , –CHF 2 , –CF 2 CH 3 , an unsubstituted methyl, an unsubstituted ethyl and –NHC(O)CH3.
- each of the aforementioned groups are substituted or unsubstituted, including any –NH group.
- can be a substituted or unsubstituted can be a substituted or [0175] Both Ring A-a and Ring B-a can be substituted or unsubstituted.
- Ring A-a and Ring B-a of can be independently substituted or unsubstituted. In some embodiments, Ring A-a and Ring B-a of can be both unsubstituted. In some embodiments, Ring A-a and Ring B-a of can be both independently substituted. In some embodiments, Ring A-a of can be substituted and Ring B of can be unsubstituted. In some embodiments, Ring A-a of can be unsubstituted and Ring B-a of can be substituted.
- Ring A of can be unsubstituted and Ring B-a of can be substituted with 1, 2 or 3 substituents independently selected from halogen, hydroxy and a substituted or unsubstituted C 1 - C6 alkyl (such as those described herein).
- Ring A-a of can be unsubstituted and Ring B-a of can be substituted with 1, 2 or 3 substituents independently selected from fluoro, hydroxy, amino, an unsubstituted N-linked amido (for example, –NHC(O)C1-C6 alkyl), an unsubstituted C1-C6 haloalkyl (such as those described herein) and an unsubstituted C1-C6 alkyl (such as those described herein).
- substituents independently selected from fluoro, hydroxy, amino, an unsubstituted N-linked amido (for example, –NHC(O)C1-C6 alkyl), an unsubstituted C1-C6 haloalkyl (such as those described herein) and an unsubstituted C1-C6 alkyl (such as those described herein).
- Ring A-a of can be unsubstituted and Ring B-a of can be substituted with 1 or 2 substituents independently selected from fluoro, hydroxy, amino, –CF 3 , –CHF 2 , –CF 2 CH 3 , an unsubstituted methyl, an unsubstituted ethyl and –NHC(O)CH3.
- R 2a can be selected from and In some embodiments, R 2a can be In some e 2a mbodiments, R can be [0177]
- Y-a can be CH or N (nitrogen). In some embodiments, Y-a can be CH.
- Y-a can be N (nitrogen).
- R 3a can be selected from halogen and a substituted or unsubstituted C 1 -C 6 alkyl (such as those described herein). In some embodiments, R 3a can be halogen. In some embodiments, R 3a can be a substituted C1-C6 alkyl (such as those described herein). In some embodiments, R 3a can be an unsubstituted C 1 -C 6 alkyl (such as those described herein). [0179] In some embodiments, m-a can be 0, 1, 2 or 3. In some embodiments, m-a can be 0. In some embodiments, m-a can be 1.
- m-a can be 2. In some embodiments, m-a can be 3. When m-a is 2 or 3, the R 3a groups can be the same or different from each other.
- X-a can be selected from hydrogen, halogen, hydroxy, cyano, a substituted or unsubstituted 4-6 membered monocyclic heterocyclyl, a substituted or unsubstituted amine(C1-C6 alkyl), a substituted or unsubstituted –NH-(CH2)1-6-amine, a mono- substituted amine, a di-substituted amine, an amino, a substituted or unsubstituted C 1 -C 6 alkyl (such as those described herein), a substituted or unsubstituted C1-C6 alkoxy (such as methoxy, ethoxy, n-propoxy, iso-propoxy, n-butoxy, iso-butoxy, sec
- X-a can be hydrogen. In other embodiments, X-a can be halogen. In some embodiments, X-a can be fluoro. In some embodiments, X-a can be chloro. In still other embodiments, X-a can be hydroxy. In yet still other embodiments, X-a can be cyano. In some embodiments, X-a can be an amino. [0182] In some embodiments, X-a can be an unsubstituted C 1 -C 6 alkyl (such as those described herein).
- X-a can be an unsubstituted methyl, an unsubstituted ethyl or an unsubstituted iso-propyl.
- X-a can be a substituted C1-C6 alkyl (such as those described herein).
- X-a can be an unsubstituted C 1 -C 6 haloalkyl (such as a C 1 -C 6 fluoroalkyl, a C 1 -C 6 chloroalkyl or a C 1 -C 6 chlorofluoroalkyl).
- X-a can be selected from –CHF2, –CF3, –CF2CH3 and –CH2CF3.
- X-a can be an unsubstituted C1-C6 hydroxyalkyl (such as a C1-C6 mono- hydroxyalkyl or a C 1 -C 6 di-hydroxyalkyl).
- X-a can be selected from – CH2OH, –CH2CH2OH, –CH(OH)CH3 and –C(OH)(CH3)2.
- X-a can be an unsubstituted C1-C6 cyanoalkyl (such as a C1-C6 mono-cyanoalkyl or a C1-C6 di-cyanoalkyl). In some embodiments, X-a can be selected from and In some embodiments, X-a can be an unsubstituted C 1 -C 6 alkoxyalkyl (such as a C 1 -C 6 mono-alkoxyalkyl or a C1-C6 di-alkoxyalkyl). In some embodiments, X-a can be selected from , and .
- X-a can be a substituted C1- C 6 alkyl selected from , , and [0183] In some embodiments, X-a can be an unsubstituted C1-C6 alkoxy (such as those described herein). In some embodiments, X-a can be an unsubstituted methoxy, an unsubstituted ethoxy or an unsubstituted iso-propoxy. In some embodiments, X-a can be a substituted C1-C6 alkoxy (such as those described herein).
- X-a can be a C1-C6 alkoxy substituted with 1, 2 or 3 substituents independently selected from halogen, an amino, a mono-substituted amine (such as those described herein) and a di-substituted amine (such as those described herein).
- X-a can be a C 1 -C 6 alkoxy substituted with 1 substituent selected from halogen, an amino, a mono-substituted amine (such as those described herein) and a di-substituted amine (such as those described herein).
- X-a can be selected from , and [0185] In some embodiments, X-a can be a substituted C3-C6 cycloalkoxy (such as those described herein). In some embodiments, X-a can be an unsubstituted C 3 -C 6 cycloalkoxy (such as those described herein). [0186] In some embodiments, X-a can be a substituted (C1-C6 alkyl)acyl, such as a substituted –(CO)-CH 3 .
- X-a can be an unsubstituted (C 1 -C 6 alkyl)acyl, such as an unsubstituted –(CO)-CH 3 .
- X-a can be a substituted 4-6 membered monocyclic heterocyclyl.
- X-a can be an unsubstituted 4-6 membered monocyclic heterocyclyl.
- X-a can be selected from azetidine, oxetane, diazetidine, azaoxetane, pyrrolidine, tetrahydrofuran, imidazoline, pyrazolidine, piperidine, tetrahydropyran, piperazine, morpholine and dioxane; wherein each of the aforementioned groups are substituted or unsubstituted, including any –NH group. .
- X-a can be selected from and ; wherein each of the aforementioned groups are substituted or unsubstituted, including any –NH group.
- X-a can be a 4-6 membered monocyclic heterocyclyl (such as those described herein) substituted with 1 or 2 substituents independently selected from halogen, a substituted or unsubstituted C1-C6 alkyl (such as those described herein), a mono- substituted amine (such as those described herein), a di-substituted amine (such as those described herein), an amino, substituted or unsubstituted amine(C 1 -C 6 alkyl) and a substituted or unsubstituted (C1-C6 alkyl)acyl.
- substituents independently selected from halogen, a substituted or unsubstituted C1-C6 alkyl (such as those described herein), a mono- substituted amine (such as those described herein), a di-substituted amine (such as those described herein), an amino, substituted or unsubstituted amine(C 1 -C 6 alkyl
- X-a can be a 4-6 membered monocyclic heterocyclyl substituted with 1 or 2 substituents independently selected from fluoro, an unsubstituted methyl, an unsubstituted ethyl, an unsubstituted iso-propyl, –CH 2 OH and – N(CH3)2.
- X-a can be selected from , , , , , and . [0189]
- X-a can be a substituted amine(C1-C6 alkyl).
- X-a can be an unsubstituted amine(C1-C6 alkyl).
- X-a can be selected from , , , , and wherein each of the aforementioned groups are substituted or unsubstituted, including any –NH group. .
- X-a can be a substituted –NH-(CH 2 ) 1-6 -amine.
- X-a can be an unsubstituted –NH-(CH 2 ) 1-6 -amine.
- X-a can be selected from and ; wherein each of the aforementioned groups are substituted or unsubstituted, including any –NH group.
- X-a can be a mono-substituted amine.
- the substituent of the mono-substituted amine is an unsubstituted C1-C6 alkyl (such as those as described herein) or an unsubstituted C3-C6 cycloalkyl (such as cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl).
- X-a can be a di-substituted amine.
- the two substituents of the di-substituted amine are independently selected from an unsubstituted C 1 -C 6 alkyl (such as those as described herein) and an unsubstituted C 3 -C 6 cycloalkyl (such as those as described herein).
- X-a can be selected from and [0194]
- X-a can be a substituted or unsubstituted C-amido.
- X-a can be a substituted or unsubstituted N-amido.
- X-a can be a substituted or unsubstituted C-carboxy.
- X-a can be a substituted or unsubstituted O-carboxy. In some embodiments, X-a can be a substituted or unsubstituted O-carbamyl. In some embodiments, X-a can be a substituted or unsubstituted N- carbamyl. In some embodiments, X-a can be mono-substituted with an unsubstituted C1-C6 hydroxyalkyl (such as those described herein). [0195] In some embodiments, Y 1-a can be CR 4A-a or N (nitrogen). In some embodiments, Y 1-a can be CR 4A-a . In some embodiments, Y 1-a can be N (nitrogen).
- Y 2-a can be CR 4B-a or N (nitrogen). In some embodiments, Y 2-a can be CR 4B-a . In some embodiments, Y 2-a can be N (nitrogen). [0197] In some embodiments, Y 1-a and Y 2-a can each be N (nitrogen). In some embodiments, Y 1-a can be CR 4A-a and Y 2-a can be CR 4B-a . In some embodiments, Y 1-a can be CR 4A-a and Y 2-a can be N (nitrogen). In some embodiments, Y 1-a can be N (nitrogen) and Y 2-a can be CR 4B-a .
- R 4A-a can be hydrogen. In some embodiments, R 4A-a can be halogen. In some embodiments, R 4A-a can be an unsubstituted C 1-4 alkyl (such as those described herein). [0199] In some embodiments, R 4B-a can be hydrogen. In some embodiments, R 4B-a can be halogen. In some embodiments, R 4B-a can be an unsubstituted C1-4 alkyl (such as those described herein). [0200] In some embodiments, R 4A-a and R 4B-a can each be hydrogen.
- R 4A-a and R 4B-a can each be halogen (wherein the halogens can be the same or different from each other).
- R 4A-a and R 4B-a can each be an unsubstituted C 1-4 alkyl (such as those described herein, and wherein the C 1-4 alkyls can be the same or different from each other).
- one of R 4A-a and R 4B-a can be hydrogen and the other of R 4A-a and R 4B-a can be halogen.
- one of R 4A-a and R 4B-a can be hydrogen and the other of R 4A-a and R 4B-a can be an unsubstituted C 1-4 alkyl (such as those described herein). In some embodiments, one of R 4A-a and R 4B-a can be halogen and the other of R 4A-a and R 4B-a can be an unsubstituted C1-4 alkyl (such as those described herein). [0201] In some embodiments, R 2a can be For exampl 2a e, R can be When R 2a is in some embodiments, R 5-a can be a substituted 5-7 membered monocyclic heterocyclyl.
- R 5-a can be an unsubstituted 5-7 membered monocyclic heterocyclyl.
- R 5-a groups include a substituted or unsubstituted piperidinyl, a substituted or unsubstituted pyrrolidinyl and a substituted or unsubstituted azepanyl.
- possible substituents include an unsubstituted C1-4 alkyl, halogen, hydroxy and unsubstituted C1-4 haloalkyl.
- Ring C-a can be selected from a substituted or unsubstituted C6-C10 aryl, a substituted or unsubstituted monocyclic 5-10 membered heteroaryl, a substituted or unsubstituted monocyclic 5-7 membered carbocyclyl, a substituted or unsubstituted 5-7 membered monocyclic heterocyclyl and a substituted or unsubstituted 7-10 membered bicyclic heterocyclyl.
- Ring C-a can be a substituted C6-C10 aryl.
- Ring C-a can be an unsubstituted C 6 -C 10 aryl.
- Ring C-a can be a substituted C 6 aryl. In some embodiments, Ring C-a can be an unsubstituted C 6 aryl. [0204] In some embodiments, Ring C-a can be a substituted 5-10 membered heteroaryl. In some embodiments, Ring C-a can be an unsubstituted 5-10 membered heteroaryl. In some embodiments, Ring C-a can be a substituted 5-6 membered heteroaryl. In some embodiments, Ring C-a can be an unsubstituted 5-6 membered heteroaryl.
- Ring C-a can be selected from furan, thiophene, pyrrole, oxazole, thiazole, imidazole, benzimidazole, indole, pyrazole, isoxazole, pyridine, pyridazine, pyrimidine, pyrazine, purine, quinoline, isoquinoline, quinazoline and quinoxaline; wherein each of the aforementioned groups are substituted or unsubstituted, including any –NH group.
- Ring C-a can be a substituted or unsubstituted monocyclic 5 membered carbocyclyl.
- Ring C-a can be a substituted or unsubstituted monocyclic 6 membered carbocyclyl. In some embodiments, Ring C-a can be a substituted or unsubstituted monocyclic 7 membered carbocyclyl. [0206] In some embodiments, Ring C-a can be a substituted or unsubstituted 5 membered monocyclic heterocyclyl. In some embodiments, Ring C-a can be a substituted or unsubstituted 6 membered monocyclic heterocyclyl. In some embodiments, Ring C-a can be a substituted or unsubstituted 7 membered monocyclic heterocyclyl.
- Ring C can be selected from imidazoline, imidazolidine, isoxazoline, isoxazolidine, oxazoline, oxazolidine, oxazolidinone, thiazoline, thiazolidine, morpholine, piperidine, piperazine, pyrrolidine, pyrrolidone, 4-piperidone, pyrazoline, pyrazolidine, tetrahydropyran, azepine, oxepine and diazepine; wherein each of the aforementioned groups are substituted or unsubstituted, including any –NH group.
- Ring C-a can be a substituted or unsubstituted 7 membered bicyclic heterocyclyl (for example, a fused, a bridged or a spiro heterocyclyl).
- Ring C-a can be a substituted or unsubstituted 8 membered bicyclic heterocyclyl, such as, a fused, a bridged or a spiro heterocyclyl.
- Ring C-a can be a substituted or unsubstituted 9 membered bicyclic heterocyclyl (for example, a fused, a bridged or a spiro heterocyclyl).
- Ring C-a can be a substituted or unsubstituted 10 membered bicyclic heterocyclyl, such as, a fused, a bridged or a spiro heterocyclyl.
- Ring C-a can be selected from pyrrolizidine, indoline, 1,2,3,4 tetrahydroquinoline, 2-azaspiro[3.3]heptane, 2-oxaspiro[3.3]heptane, 2-oxa-6- azaspiro[3.3]heptane, 2,6-diazaspiro[3.3]heptane, 2-oxaspiro[3.4]octane and 2- azaspiro[3.4]octane; wherein each of the aforementioned groups are substituted or unsubstituted, including any –NH group.
- Ring C-a can be substituted with one or more substituents independently selected from an unsubstituted C 1 -C 6 alkyl (as described herein) and an unsubstituted (C1-C6 alkyl)acyl. In some embodiments, Ring C-a can be substituted with one substituent selected from an unsubstituted C1-C6 alkyl (as described herein) and an unsubstituted (C 1 -C 6 alkyl)acyl. [0209] In some embodiments, R 2a can be selected from: , , and wherein each of the aforementioned groups can be substituted or unsubstituted.
- Compound (A), including pharmaceutically acceptable salts thereof can be administered prior to all of Compound (B), or a pharmaceutically acceptable salt thereof.
- Compound (A), including pharmaceutically acceptable salts thereof can be administered prior to at least one Compound (B), or a pharmaceutically acceptable salt thereof.
- Compound (A), including pharmaceutically acceptable salts thereof can be administered concomitantly with Compound (B), or a pharmaceutically acceptable salt thereof.
- Compound (A), including pharmaceutically acceptable salts thereof can be administered subsequent to the administration of at least one Compound (B), or a pharmaceutically acceptable salt thereof.
- Compound (A), including pharmaceutically acceptable salts thereof can be administered subsequent to the administration of all Compound (B), or a pharmaceutically acceptable salt thereof.
- Compound (B), including pharmaceutically acceptable salts thereof can be administered subsequent to the administration of all Compound (B), or a pharmaceutically acceptable salt thereof.
- a combination as described herein of Compound (A), including pharmaceutically acceptable salts thereof, and one or more of Compound (B), or pharmaceutically acceptable salts thereof can decrease the number and/or severity of side effects that can be attributed to a compound described herein, such as Compound (B), or a pharmaceutically acceptable salt thereof.
- Using a combination of compounds described herein can results in additive, synergistic or strongly synergistic effect.
- a combination of compounds described herein can result in an effect that is not antagonistic.
- a combination as described herein of Compound (A), including pharmaceutically acceptable salts thereof, and one or more of Compound (B), or pharmaceutically acceptable salts thereof can result in an additive effect.
- a combination as described herein of Compound (A), including pharmaceutically acceptable salts thereof, and one or more of Compound (B), or pharmaceutically acceptable salts thereof can result in a synergistic effect.
- a combination as described herein of Compound (A), including pharmaceutically acceptable salts thereof, and one or more of Compound (B), or pharmaceutically acceptable salts thereof can result in a strongly synergistic effect.
- a combination as described herein of Compound (A), including pharmaceutically acceptable salts thereof, and one or more of Compound (B), or pharmaceutically acceptable salts thereof is not antagonistic.
- the term “antagonistic” means that the activity of the combination of compounds is less compared to the sum of the activities of the compounds in combination when the activity of each compound is determined individually (i.e., as a single compound).
- the term “synergistic effect” means that the activity of the combination of compounds is greater than the sum of the individual activities of the compounds in the combination when the activity of each compound is determined individually.
- the term “additive effect” means that the activity of the combination of compounds is about equal to the sum of the individual activities of the compounds in the combination when the activity of each compound is determined individually.
- a potential advantage of utilizing a combination as described herein may be a reduction in the required amount(s) of the compound(s) that is effective in treating a disease condition disclosed herein compared to when each compound is administered as a monotherapy.
- the amount of Compound (B), or a pharmaceutically acceptable salt thereof, used in a combination described herein can be less compared to the amount of Compound (B), or a pharmaceutically acceptable salt thereof, needed to achieve the same reduction in a disease marker (for example, tumor size) when administered as a monotherapy.
- Another potential advantage of utilizing a combination as described herein is that the use of two or more compounds having different mechanisms of action can create a higher barrier to the development of resistance compared to when a compound is administered as monotherapy.
- compositions [0221] Compound (A), including pharmaceutically acceptable salts thereof, can be provided in a pharmaceutical composition. Likewise, Compound (B), including pharmaceutically acceptable salts thereof, can be provided in a pharmaceutical composition.
- pharmaceutical composition refers to a mixture of one or more compounds and/or salts disclosed herein with other chemical components, such as diluents, carriers and/or excipients. The pharmaceutical composition facilitates administration of the compound to an organism.
- compositions can also be obtained by reacting compounds with inorganic or organic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, and salicylic acid.
- Pharmaceutical compositions will generally be tailored to the specific intended route of administration.
- a “carrier” refers to a compound that facilitates the incorporation of a compound into cells or tissues.
- DMSO dimethyl sulfoxide
- a “diluent” refers to an ingredient in a pharmaceutical composition that lacks appreciable pharmacological activity but may be pharmaceutically necessary or desirable.
- a diluent may be used to increase the bulk of a potent drug whose mass is too small for manufacture and/or administration. It may also be a liquid for the dissolution of a drug to be administered by injection, ingestion or inhalation.
- a common form of diluent in the art is a buffered aqueous solution such as, without limitation, phosphate buffered saline that mimics the pH and isotonicity of human blood.
- an “excipient” refers to an essentially inert substance that is added to a pharmaceutical composition to provide, without limitation, bulk, consistency, stability, binding ability, lubrication, disintegrating ability etc., to the composition.
- stabilizers such as anti-oxidants and metal-chelating agents are excipients.
- the pharmaceutical composition comprises an anti-oxidant and/or a metal-chelating agent.
- a “diluent” is a type of excipient.
- Compound (B), along with pharmaceutically acceptable salts thereof can be provided in a pharmaceutical composition that includes Compound (A), including pharmaceutically acceptable salts thereof.
- Compound (B), along with pharmaceutically acceptable salts thereof, can be administered in a pharmaceutical composition that is separate from a pharmaceutical composition that includes Compound (A), including pharmaceutically acceptable salts thereof.
- the pharmaceutical compositions described herein can be administered to a human patient per se, or in pharmaceutical compositions where they are mixed with other active ingredients, as in combination therapy, or carriers, diluents, excipients or combinations thereof. Proper formulation is dependent upon the route of administration chosen. Techniques for formulation and administration of the compounds described herein are known to those skilled in the art.
- compositions disclosed herein may be manufactured in a manner that is itself known, e.g., by means of conventional mixing, dissolving, granulating, dragee-making, levigating, emulsifying, encapsulating, entrapping or tableting processes. Additionally, the active ingredients are contained in an amount effective to achieve its intended purpose. Many of the compounds used in the pharmaceutical combinations disclosed herein may be provided as salts with pharmaceutically compatible counterions.
- Compound (A), including pharmaceutically acceptable salts thereof can be administered orally.
- Compound (A), including pharmaceutically acceptable salts thereof can be provided to a subject by the same route of administration as Compound (B), along with pharmaceutically acceptable salts thereof.
- Compound (A), including pharmaceutically acceptable salts thereof can be provided to a subject by a different route of administration as Compound (B), along with pharmaceutically acceptable salts thereof.
- compositions may, if desired, be presented in a pack or dispenser device which may contain one or more unit dosage forms containing the active ingredient.
- the pack may for example comprise metal or plastic foil, such as a blister pack.
- the pack or dispenser device may be accompanied by instructions for administration.
- the pack or dispenser may also be accompanied with a notice associated with the container in form prescribed by a governmental agency regulating the manufacture, use, or sale of pharmaceuticals, which notice is reflective of approval by the agency of the form of the drug for human or veterinary administration.
- Such notice for example, may be the labeling approved by the U.S. Food and Drug Administration for prescription drugs, or the approved product insert.
- compositions that can include a compound and/or salt described herein formulated in a compatible pharmaceutical carrier may also be prepared, placed in an appropriate container, and labeled for treatment of an indicated condition.
- a combination of compounds that includes an effective amount of Compound (A), including pharmaceutically acceptable salts thereof, and an effective amount of one or more of Compound (B), or a pharmaceutically acceptable salt thereof, can be used to treat a disease or condition.
- diseases or conditions that can be treated by a combination of compounds, along with pharmaceutically acceptable salts thereof, include malignancies, cancers and syndromes such as those described herein.
- the disease or condition can be a hematological malignancy.
- Exemplary hematological malignancies include is a leukemia, a lymphoma, or a myeloma.
- the hematological malignancy can be refractory.
- the disease or condition can be a leukemia including, but not limited to: acute myeloid leukemia (AML) (including its subtypes, such as, subtypes TP53 wildtype AML, TP53 mutant AML, refractory AML, acute promyelocytic leukemia, acute basophilic leukemia, and therapy-related AML), chronic lymphocytic leukemia (CLL) (including, but not limited to hairy cell leukemia and small lymphocytic lymphoma), acute lymphoblastic leukemia (ALL) (including, but not limited to specification for B-cell, T-cell, and ETP) and chronic myeloid leukemia (CML) (chronic myelogenous leukemia).
- AML acute myeloid leukemia
- CLL chronic lymph
- the disease or condition can be a Myelodysplastic syndrome.
- the disease or condition can be a myeloproliferative neoplasm (MPN), such as polycythemia vera (PV), myelofibrosis (MF) and essential thrombocythemia (ET).
- MPN myeloproliferative neoplasm
- PV polycythemia vera
- MF myelofibrosis
- ET essential thrombocythemia
- a combination of compounds described herein can be used to treat and/or ameliorate a lymphoma.
- Exemplary lymphomas include, but are not limited to, a non-Hodgkin’s lymphoma (NHL) (including, but not limited to mantle cell lymphoma (MCL), diffuse large B-cell lymphoma (DLBCL), follicular lymphoma (FL), marginal zone lymphoma (MZL), peripheral T-cell lymphoma, cutaneous T-cell lymphoma, NK lymphoma, Burkitt lymphoma and Waldenstrom’s macroglobulinemia).
- NHL non-Hodgkin’s lymphoma
- MCL mantle cell lymphoma
- DLBCL diffuse large B-cell lymphoma
- FL follicular lymphoma
- MZL marginal zone lymphoma
- peripheral T-cell lymphoma cutaneous T-cell lymphoma
- NK lymphoma Burkitt lymphoma
- Waldenstrom Waldenstrom’s macroglobulinemia
- myelomas examples include, but are not limited to, multiple myeloma (MM) (including but not limited to translocation(11;14) and non-translocation(11;14)).
- MM multiple myeloma
- a combination of compounds described herein can be used to treat and/or ameliorate a systemic mastocytosis, and blastic plasmacytoid dendritic cell neoplasm.
- a disease or condition described herein can be in an adult or pediatric subject.
- the subject that suffers from the disease or condition, such as those described herein can be a pediatric subject.
- the disease or condition can be a pediatric hematological malignancy, for example, pediatric AML and/or pediatric ALL.
- a combination of compounds described herein can be used to treat and/or ameliorate a solid tumor.
- the solid tumor can be selected from an Ewing's tumor and a Wilms' cancer.
- Additional examples of a solid tumor that can be treated by a combination of compounds described herein, including pharmaceutically acceptable salts thereof, are a bladder cancer, a brain cancer, a breast cancer (including but not limited to ER+ breast cancer and triple negative breast cancer), a cervical cancer, a choriocarcinoma, a cervicocerebral cancer, a colon cancer, an endometrial cancer, an esophageal cancer, a gallbladder/bile duct cancer, a head and neck cancer (including oral cancer), a hepatocellular cancer, a lung cancer (including a non-small cell cancer and small-cell lung cancer), a mesothelioma, an ovarian cancer, an osteosarcoma, a pancreatic cancer, a penis cancer
- the disease or condition can be a cancer that expresses BCL-2 protein.
- a “subject” refers to an animal that is the object of treatment, observation or experiment.
- Animal includes cold- and warm-blooded vertebrates and invertebrates such as fish, shellfish, reptiles and, in particular, mammals.
- “Mammal” includes, without limitation, mice, rats, rabbits, guinea pigs, dogs, cats, sheep, goats, cows, horses, primates, such as monkeys, chimpanzees, and apes, and, in particular, humans.
- the subject can be human.
- the subject can be a child and/or an infant, for example, a child or infant with a fever. In other embodiments, the subject can be an adult.
- the terms “treat,” “treating,” “treatment,” “therapeutic,” and “therapy” do not necessarily mean total cure or abolition of the disease or condition. Any alleviation of any undesired signs or symptoms of the disease or condition, to any extent can be considered treatment and/or therapy. Furthermore, treatment may include acts that may worsen the subject’s overall feeling of well-being or appearance.
- the term “effective amount” is used to indicate an amount of an active compound, or pharmaceutical agent, that elicits the biological or medicinal response indicated.
- an effective amount of compound, salt or composition can be the amount needed to prevent, alleviate or ameliorate symptoms of the disease or condition, or prolong the survival of the subject being treated.
- This response may occur in a tissue, system, animal or human and includes alleviation of the signs or symptoms of the disease or condition being treated. Determination of an effective amount is well within the capability of those skilled in the art, in view of the disclosure provided herein.
- the effective amount of the compounds disclosed herein required as a dose will depend on the route of administration, the type of animal, including human, being treated and the physical characteristics of the specific animal under consideration. The dose can be tailored to achieve a desired effect, but will depend on such factors as weight, diet, concurrent medication and other factors which those skilled in the medical arts will recognize.
- an effective amount of a compound, or radiation is the amount that results in: (a) the reduction, alleviation or disappearance of one or more symptoms caused by the cancer, (b) the reduction of tumor size, (c) the elimination of the tumor, and/or (d) long-term disease stabilization (growth arrest) of the tumor.
- the amount of compound, salt and/or composition required for use in treatment will vary not only with the particular compound or salt selected but also with the route of administration, the nature and/or symptoms of the disease or condition being treated and the age and condition of the patient and will be ultimately at the discretion of the attendant physician or clinician. In cases of administration of a pharmaceutically acceptable salt, dosages may be calculated as the free base.
- Compound (A) and Compound (B), along with pharmaceutically acceptable salts thereof can be used in a combination described herein.
- Compound (A), or a pharmaceutically acceptable salt thereof can be dosed in an amount in the range of 20-500 mg/day.
- Compound (B), or a pharmaceutically acceptable salt thereof can be dosed in an amount in the range of 20-500 mg/day.
- Compound (A) and/or Compound (B), including pharmaceutically acceptable salts thereof can be dosage at about 50 mg/day, about 60 mg/day, about 70 mg/day, about 80 mg/day, about 90 mg/day, about 100 mg/day, about 110 mg/day, about 120 mg/day, about 130 mg/day, about 140 mg/day, about 150 mg/day, about 160 mg/day, about 170 mg/day, about 180 mg/day, about 190 mg/day, about 200 mg/day, about 210 mg/day, about 220 mg/day, about 230 mg/day, about 240 mg/day, about 250 mg/day, about 260 mg/day, about 270 mg/day, about 280 mg/day, about 290 mg/day, about 300 mg/day, about 310 mg/day, about 320 mg/day, about 330 mg/day, about 340 mg/day, about 350 mg/day, about 360 mg/day, about 370 mg/day, about 380 mg/day, about 390 mg/day,
- Compound (A), or a pharmaceutically acceptable salt thereof can be dosed in an amount in the range of 200-400 mg/day. In some embodiments, Compound (B), or a pharmaceutically acceptable salt thereof, can be dosed in an amount in the range of 200-400 mg/day. [0244] Various dosages of Compound (A) and Compound (B), along with pharmaceutically acceptable salts thereof, can be used in a combination described herein. In some embodiments, Compound (A), or a pharmaceutically acceptable salt thereof, can be dosed in an amount in the range of 20-500 mg. In some embodiments, Compound (B), or a pharmaceutically acceptable salt thereof, can be dosed in an amount in the range of 20-500 mg.
- Compound (A) and/or Compound (B), including pharmaceutically acceptable salts thereof can be dosage at about 50 mg, about 60 mg, about 70 mg, about 80 mg, about 90 mg, about 100 mg, about 110 mg, about 120 mg, about 130 mg, about 140 mg, about 150 mg, about 160 mg, about 170 mg, about 180 mg, about 190 mg, about 200 mg, about 210 mg, about 220 mg, about 230 mg, about 240 mg, about 250 mg, about 260 mg, about 270 mg, about 280 mg, about 290 mg, about 300 mg, about 310 mg, about 320 mg, about 330 mg, about 340 mg, about 350 mg, about 360 mg, about 370 mg, about 380 mg, about 390 mg, about 400 mg, about 410 mg, about 420 mg, about 430 mg, about 440 mg, about 450 mg, about 460 mg, about 470 mg, about 480 mg, about 490 mg, or about 500 mg.
- Compound (A), or a pharmaceutically acceptable salt thereof can be dosed in an amount in the range of 200-400 mg. In some embodiments, Compound (B), or a pharmaceutically acceptable salt thereof, can be dosed in an amount in the range of 200-400 mg. [0245] As will be readily apparent to one skilled in the art, the useful in vivo dosage to be administered and the particular mode of administration will vary depending upon the age, weight, the severity of the affliction, the mammalian species treated, the particular compounds employed and the specific use for which these compounds are employed.
- effective dosage levels that is the dosage levels necessary to achieve the desired result
- useful dosages of compounds (A) and/or (B), or pharmaceutically acceptable salts of any of the foregoing can be determined by comparing their in vitro activity, and in vivo activity in animal models. Such comparison can be done by comparison against an established drug, such as cisplatin and/or gemcitabine) [0246] Dosage amount and interval may be adjusted individually to provide plasma levels of the active moiety which are sufficient to maintain the modulating effects, or minimal effective concentration (MEC).
- MEC minimal effective concentration
- the MEC will vary for each compound but can be estimated from in vivo and/or in vitro data. Dosages necessary to achieve the MEC will depend on individual characteristics and route of administration. However, HPLC assays or bioassays can be used to determine plasma concentrations. Dosage intervals can also be determined using MEC value. Compositions should be administered using a regimen which maintains plasma levels above the MEC for 10-90% of the time, preferably between 30-90% and most preferably between 50-90%. In cases of local administration or selective uptake, the effective local concentration of the drug may not be related to plasma concentration. [0247] It should be noted that the attending physician would know how to and when to terminate, interrupt or adjust administration due to toxicity or organ dysfunctions.
- the magnitude of an administrated dose in the management of the disorder of interest will vary with the severity of the disease or condition to be treated and to the route of administration.
- the severity of the disease or condition may, for example, be evaluated, in part, by standard prognostic evaluation methods.
- the dose and perhaps dose frequency will also vary according to the age, body weight and response of the individual patient. A program comparable to that discussed above may be used in veterinary medicine.
- Compounds, salts and compositions disclosed herein can be evaluated for efficacy and toxicity using known methods.
- the toxicology of a particular compound, or of a subset of the compounds, sharing certain chemical moieties may be established by determining in vitro toxicity towards a cell line, such as a mammalian, and preferably human, cell line.
- a cell line such as a mammalian, and preferably human, cell line.
- the results of such studies are often predictive of toxicity in animals, such as mammals, or more specifically, humans.
- the toxicity of particular compounds in an animal model such as mice, rats, rabbits, dogs or monkeys, may be determined using known methods.
- the efficacy of a particular compound may be established using several recognized methods, such as in vitro methods, animal models, or human clinical trials.
- CTG assay Cell proliferation was measured using the CellTiter-Glo® Luminescent Cell Viability Assay. The assay involved the addition of a single reagent (CellTiter-Glo® Reagent) directly to cells cultured in serum-supplemented medium. RS4;11 (ATC, CRL-1873) cells were cultured according to ATCC recommendations and were seeded at 50,000 cells per well.
- MV4- 11 (ATCC, CRL-9591), Toledo (ATCC, CRL-2631), MCF-7 (ATCC, HTB-22) and DMS-53 (ATCC, CRL-2062) cells were cultured according to ATCC recommendations and were seeded at 20,000 cells per well.
- Compound 5 (free base) and Compound 1a (free base) were prepared as a DMSO stock solution (10 mM).
- DMSO stock solution 10 mM
- the MCF-7 combination assay was performed in duplicate with a 10-point serial dilution curve (1:3 dilution) for Compounds 5 and 1a, and a 10-point serial dilution curve (1:5 dilution) when treated in combination.
- the highest compound concentration was 10 ⁇ M with a 0.1% final DMSO concentration. Plates were incubated at 37 °C, 5% CO2 for 72 h and then equilibrated at room temperature for approximately 30 min. An equal-volume amount of CellTiter-Glo® Reagent (100 ⁇ L) was added to each well. Plates were mixed for 2 min on an orbital shaker to induce cell lysis and then incubated at room temperature for 10 min to stabilize the luminescent signal.
- mice were inoculated with HL-60 cells subcutaneously on the right flank with the single cell suspension of 95% viable tumor cells (1 ⁇ 10 7 ) in 100 ⁇ L IMDM Matrigel mixture (1:1 ratio) without serum for the tumor development. The treatment was started when the mean tumor size reached approximately 215 mm 3 , with individual tumor size ranging from 185-245 mm 3 . Animals were randomly distributed into treatment groups of 10 animals each and dosed with vehicle and indicated compounds at indicated dosage and frequency shown in Figure 5 and Table 4. Compound 5 was dosed as a free base and Compound 1a was dosed as a free base.
- the bottom line represents data for Compound 5 (50 mg/kg) + Compound 1a (80 mg/kg)
- the second line from the bottom (indicated with triangles) represents data for Compound 5 (50 mg/kg) + Compound 1a (60 mg/kg)
- the third line from the bottom (indicated with diamonds) represents data for Compound 5 (50 mg/kg).
- Tumor volumes were evaluated twice per week to calculate tumor volume over time, and mice were weighed twice per week as a surrogate for signs of toxicity.
- Td and Cd are the mean tumor volumes of the treated and control animals, and T0 and C0 are the mean tumor volumes of the treated and control animals at the start of the experiment.
- the tumor regression was defined as individual tumor volume (TV) decrease (terminal TV compared to initial TV).
- the percent tumor regression was calculated using the formula: (1 - (Td / T0)) ⁇ 100%.
- Figure 5 and Table 4 illustrate that single agent treatment of Compound 1a at 60 or 80 mg/kg did not result in tumor growth inhibition and single agent treatment with Compound 5 resulted in minor efficacy (30%).
- the combination of Compound 5 (50 mg/kg) and Compound 1a (60 mg/kg) exhibited significant TGI and resulted in the complete regression of 8 out of 10 tumors on day 18.
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Publication number | Priority date | Publication date | Assignee | Title |
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WO2023083194A1 (en) * | 2021-11-09 | 2023-05-19 | 杭州格博生物医药有限公司 | Wee1 protein kinase degradation agent and use thereof |
WO2023114877A1 (en) * | 2021-12-15 | 2023-06-22 | Recurium Ip Holdings, Llc | Triple therapy combinations of bcl-2 inhibitors, wee-1 inhibitors and other chemotherapeutic agents |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019139899A1 (en) * | 2018-01-10 | 2019-07-18 | Zeno Royalties & Milestones, LLC | Benzamide compounds |
WO2019173082A1 (en) * | 2018-03-09 | 2019-09-12 | Zeno Royalties & Milestones, LLC | Substituted l,2-dihydro-3h-pyrazolo[3,4-d]pyrimidin-3-ones |
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CN109422754A (en) * | 2017-08-24 | 2019-03-05 | 上海迪诺医药科技有限公司 | Pyrazolo [3,4-d] pyrimidine -3- ketone derivatives, its pharmaceutical composition and application |
EP3694861A4 (en) * | 2017-10-09 | 2021-05-19 | Nuvation Bio Inc. | Heterocyclic compounds and uses thereof |
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Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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WO2019173082A1 (en) * | 2018-03-09 | 2019-09-12 | Zeno Royalties & Milestones, LLC | Substituted l,2-dihydro-3h-pyrazolo[3,4-d]pyrimidin-3-ones |
Non-Patent Citations (5)
Title |
---|
DE JONG MATHILDE RIKJE WILLEMIJN, LANGENDONK MYRA, REITSMA BART, HERBERS PIEN, NIJLAND MARCEL, HULS GERWIN, VAN DEN BERG ANKE, AMM: "WEE1 Inhibition Enhances Anti-Apoptotic Dependency as a Result of Premature Mitotic Entry and DNA Damage", CANCERS, vol. 11, no. 11, pages 1743, XP055843116, DOI: 10.3390/cancers11111743 * |
GEENEN JILL J.J., SCHELLENS JAN H.M.: "Molecular Pathways: Targeting the Protein Kinase Wee1 in Cancer", CLINICAL CANCER RESEARCH, AMERICAN ASSOCIATION FOR CANCER RESEARCH, US, vol. 23, no. 16, 15 August 2017 (2017-08-15), US, pages 4540 - 4544, XP055843092, ISSN: 1078-0432, DOI: 10.1158/1078-0432.CCR-17-0520 * |
GHIASI NAGHMEH, HABIBAGAHI MOJTABA, ROSLI ROZITA, GHADERI ABBAS, YUSOFF KHATIJAH, HOSSEINI AHMAD, ABDULLAH SYAHRILNIZAM, JABERIPOU: "Tumour Suppressive Effects of WEE1 Gene Silencing in Breast Cancer Cells", ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, TH, vol. 14, no. 11, 30 November 2013 (2013-11-30), TH, pages 6605 - 6611, XP055843098, ISSN: 1513-7368, DOI: 10.7314/APJCP.2013.14.11.6605 * |
PERINI ET AL: "BCL-2 as therapeutic target for hematological malignancies", vol. 11, no. 65, 11 May 2018 (2018-05-11), pages 1 - 15, XP002797218, DOI: 10.1186/s13045-018-0608-2 * |
See also references of EP4069235A4 * |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11261192B2 (en) | 2018-03-09 | 2022-03-01 | Recurium Ip Holdings, Llc | Substituted 1,2-dihydro-3H-pyrazolo[3,4-D]pyrimidin-3-ones |
WO2023083194A1 (en) * | 2021-11-09 | 2023-05-19 | 杭州格博生物医药有限公司 | Wee1 protein kinase degradation agent and use thereof |
WO2023114877A1 (en) * | 2021-12-15 | 2023-06-22 | Recurium Ip Holdings, Llc | Triple therapy combinations of bcl-2 inhibitors, wee-1 inhibitors and other chemotherapeutic agents |
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