WO2021058021A1 - 包含tlr7激动剂的药物组合 - Google Patents
包含tlr7激动剂的药物组合 Download PDFInfo
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- WO2021058021A1 WO2021058021A1 PCT/CN2020/118693 CN2020118693W WO2021058021A1 WO 2021058021 A1 WO2021058021 A1 WO 2021058021A1 CN 2020118693 W CN2020118693 W CN 2020118693W WO 2021058021 A1 WO2021058021 A1 WO 2021058021A1
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- pyrrolo
- butoxy
- amine
- pyrimidin
- pharmaceutically acceptable
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- QDGZDCVAUDNJFG-WPZUCAASSA-N C=C([C@H](CO)C(C1)O)[C@H]1[n]1c(N=C(N)NC2=O)c2nc1 Chemical compound C=C([C@H](CO)C(C1)O)[C@H]1[n]1c(N=C(N)NC2=O)c2nc1 QDGZDCVAUDNJFG-WPZUCAASSA-N 0.000 description 1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- 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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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- 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
- A61K31/52—Purines, e.g. adenine
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- 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
- A61K31/52—Purines, e.g. adenine
- A61K31/522—Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/28—Dragees; Coated pills or tablets, e.g. with film or compression coating
- A61K9/2893—Tablet coating processes
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/20—Antivirals for DNA viruses
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Definitions
- This application belongs to the field of medicinal chemistry and relates to a drug combination containing TLR7 agonists. Specifically, it relates to a combination of a compound of formula I as a TLR7 agonist and entecavir for the treatment of hepatitis B virus infection and its use.
- HBV hepatitis B virus
- Nucleoside (acid) drugs such as Entecavir, can inhibit HBV DNA replication.
- Toll-like receptors are expressed in a variety of immune cells. Toll-like receptors recognize highly conserved structural motifs: pathogen-related microbial patterns (PAMP) expressed by microbial pathogens or damage-related molecular patterns (DAMP) released by necrotic cells. Stimulating Toll-like receptors through the corresponding pathogen-associated microbial pattern (PAMP) or damage-associated molecular pattern (DAMP) to trigger a signal cascade leading to transcription factors such as AP-1, NF- ⁇ B and interferon regulatory factors (impulse response function) activation. This leads to a variety of cellular responses, including the production of interferons, pro-inflammatory cytokines, and effector cytokines, leading to immune responses.
- PAMP pathogen-related microbial patterns
- DAMP damage-related molecular patterns
- Toll-like receptors 1 1 and 6 are mainly expressed on the cell surface, and Toll-like receptors 3, 7, 8 and 9 are expressed in endosomes.
- Different Toll-like receptors recognize ligands derived from different pathogens.
- TLR7 TLR7
- pDC plasmacytoid dendritic cell
- IFN- ⁇ interferon- ⁇
- TLR7 agonists have been reported, such as Imiquimod, resiquimod, GS-9620 and so on.
- WO2016023511 and WO2017076346 disclose a new class of TLR7 agonists, the compounds exhibiting good biological activity and selectivity.
- the application provides a pharmaceutical combination, which includes a compound of formula I or a pharmaceutically acceptable salt thereof and entecavir or a pharmaceutically acceptable salt or solvate thereof.
- the application also provides the use of the drug combination of the application in the preparation of a medicament for the treatment of hepatitis B virus infection.
- the present application also provides a method for treating hepatitis B virus infection, which includes administering an effective amount of the drug combination of the present application to an individual in need.
- the application also provides a drug combination for the treatment of hepatitis B virus infection.
- the application also provides the use of the drug combination of the application for the treatment of hepatitis B virus infection.
- the application provides a pharmaceutical combination, which includes a compound of formula I or a pharmaceutically acceptable salt thereof and entecavir or a pharmaceutically acceptable salt or solvate thereof.
- a pharmaceutical combination which includes a compound of formula I or a pharmaceutically acceptable salt thereof and entecavir or a pharmaceutically acceptable salt or solvate thereof.
- the compound of formula I is as follows:
- L 1 is selected from -O-;
- L 2 is selected from -CH 2 -, wherein the above -CH 2 -is optionally substituted by R 4;
- R 1 is selected from hydrogen or C 1-10 alkyl, wherein the above C 1-10 alkyl is optionally substituted by R 5;
- R 2 is selected from hydrogen, cyano, -COOH, or -CONH 2 , wherein the aforementioned -COOH, and -CONH 2 are optionally substituted by R 6;
- B is selected from 6-10 membered aryl groups or 5-10 membered heteroaryl groups
- L 3 is selected from a C 0-6 alkylene group or an imino group, wherein the aforementioned C 0-6 alkylene group and imino group are optionally substituted by R 7;
- R 3 is selected from hydrogen, amino, C 1-10 alkyl, C 3-10 cyclic hydrocarbon group, 3-10 membered heterocyclic hydrocarbon group, 6-10 membered aryl group, or 5-10 membered heteroaryl group, wherein the above-mentioned amino group, A C 1-10 alkyl group, a C 3-10 cycloalkyl group, a 3-10 membered heterocyclic hydrocarbon group, a 6-10 membered aryl group, or a 5-10 membered heteroaryl group are optionally substituted by R 8 or,
- R 3 and L 3 form a saturated or unsaturated 5-8 membered ring together with the adjacent atoms on the B ring, and the 5-8 membered ring is optionally substituted by R 9;
- n 0, 1, 2, 3, 4 or 5;
- R is independently selected from C 1-8 alkyl, C 3-8 cyclic hydrocarbon group, 3-8 membered heterocyclic hydrocarbon group, 6-8 membered aryl group, 5-8 membered heteroaryl group.
- L 2 is selected from -CH 2 -.
- R 1 is selected from C 1-6 alkyl, wherein the aforementioned C 1-6 alkyl is optionally substituted with one or more R 5 .
- R 2 is selected from hydrogen, cyano, or -CONH 2 , wherein the aforementioned -CONH 2 is optionally substituted with one or more R 6 .
- B is selected from 6-7 membered aryl, or 5-7 membered heteroaryl.
- B is selected from phenyl, pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, thienyl, thiazolyl, furyl, oxazolyl, thiadiazolyl, isooxanyl Azolyl, oxadiazolyl, pyrrolyl, imidazolyl, pyrazolyl, isothiazolyl, or triazolyl.
- B is selected from phenyl, pyridyl, or thiazolyl.
- L 3 is selected from Co -6 alkylene, wherein the aforementioned Co -6 alkylene is optionally substituted with one or more R 7 .
- R 3 is selected from hydrogen, amino, C 1-6 alkyl, C 3-8 cycloalkyl, 3-8 membered heterocycloalkyl, 6-8 membered aryl, or 5- 8-membered heteroaryl group, wherein the above-mentioned amino group, C 1-6 alkyl group, C 3-8 cycloalkyl group, 3-8 membered heterocyclic hydrocarbon group, 6-8 membered aryl group, or 5-8 membered heteroaryl group are optionally One or more R 8 substitutions; or R 3 , L 3 and the adjacent atoms on the B ring together form a saturated or unsaturated 5-8 membered ring, the 5-8 membered ring is optionally substituted by one or more R 9 replaces.
- R 3 is selected from hydrogen, amino, C 1-6 alkyl, piperazinyl, morpholinyl, tetrahydropyrrolyl, piperidinyl, azetidinyl, diazide Heterocycloheptyl, or 2-oxa-5-azabicyclo[2.2.1]heptyl, wherein the above-mentioned amino, C 1-6 alkyl, piperazinyl, morpholinyl, tetrahydropyrrolyl, Piperidinyl, azetidinyl, diazacycloheptanyl, or 2-oxa-5-azabicyclo[2.2.1]heptyl is optionally substituted with one or more R 8 ; or R 3 , L 3 and the adjacent atoms on the B ring together form a saturated or unsaturated 6-membered ring, and the 6-membered ring is optionally substituted by one or more R 9 .
- the compound of formula I or a pharmaceutically acceptable salt thereof is selected from:
- the compound of formula I or a pharmaceutically acceptable salt thereof is selected from 2-butoxy-7-(4-(pyrrolidin-1-ylmethyl)benzyl)-5H -Pyrrolo[3,2-d]pyrimidin-4-amine or a pharmaceutically acceptable salt thereof, or 2-butoxy-7-((2-(pyrrolidin-1-ylmethyl)thiazole-5 -(Yl)methyl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine or a pharmaceutically acceptable salt thereof.
- the entecavir solvate is selected from entecavir hydrate. In some embodiments, the entecavir hydrate is selected from entecavir 0.5-2 hydrate. The entecavir hydrate is selected from entecavir monohydrate.
- the pharmaceutically acceptable salt of Entecavir is selected from maleate. In some embodiments of the application, the pharmaceutically acceptable salt of Entecavir is selected from monomaleate.
- entecavir or a pharmaceutically acceptable salt or solvate thereof is selected from entecavir-maleate, entecavir-monohydrate, or entecavir-maleate monohydrate.
- the pharmaceutical combination includes 2-butoxy-7-(4-(pyrrolidin-1-ylmethyl)benzyl)-5H-pyrrolo[3,2-d] Pyrimidine-4-amine or a pharmaceutically acceptable salt thereof, and Entecavir or a pharmaceutically acceptable salt or solvate thereof.
- the pharmaceutical combination described herein includes 2-butoxy-7-(4-(pyrrolidin-1-ylmethyl)benzyl)-5H-pyrrolo[3,2-d] Pyrimidine-4-amine, or its maleate, trifluoroacetate, and entecavir or its pharmaceutically acceptable salt or hydrate.
- the pharmaceutical combination described herein includes 2-butoxy-7-(4-(pyrrolidin-1-ylmethyl)benzyl)-5H-pyrrolo[3,2-d] Pyrimidine-4-amine and Entecavir or its monohydrate.
- the pharmaceutical combination includes 2-butoxy-7-((2-(pyrrolidin-1-ylmethyl)thiazol-5-yl)methyl)-5H-pyrrolo [3,2-d] Pyrimidine-4-amine or a pharmaceutically acceptable salt thereof, and Entecavir or a solvate thereof.
- the pharmaceutical combination described herein includes 2-butoxy-7-((2-(pyrrolidin-1-ylmethyl)thiazol-5-yl)methyl)-5H-pyrrolo [3,2-d]pyrimidin-4-amine and entecavir-maleate monohydrate.
- the compound of formula I of the drug combination or a pharmaceutically acceptable salt thereof can be administered once a day, twice a day, once every two days, once every three days, every It is administered once every four days, or once every five days, and each administration is 0.0001 to 20 mg/kg weight (calculated based on the weight of the compound of formula I).
- the entecavir or its pharmaceutically acceptable salt or solvate of the drug combination can be administered once a day, twice a day, or once every two days, each time 0.5 mg or 1.0 mg Specification dosage (calculated by weight of entecavir).
- the average daily dose of entecavir or a pharmaceutically acceptable salt or solvate thereof of the drug combination is 0.005 mg to 10.0 mg. In some embodiments of the application, the average daily dose of entecavir or a pharmaceutically acceptable salt or solvate thereof of the drug combination is 0.05 mg to 5.0 mg. In some embodiments of the present application, the average daily dose of entecavir or a pharmaceutically acceptable salt or solvate thereof of the drug combination is 0.10 mg to 2.0 mg. In some embodiments of the application, the average daily dose of entecavir or a pharmaceutically acceptable salt or solvate thereof of the drug combination is 0.25 mg to 2.0 mg. In some embodiments of the application, the average daily dose of entecavir or a pharmaceutically acceptable salt or solvate thereof of the drug combination is 0.5 mg to 1.0 mg.
- the ratio of the average daily dose of the compound of formula I or its pharmaceutically acceptable salt to entecavir or its pharmaceutically acceptable salt or solvate (in units of weight) in the pharmaceutical combination is selected from 10 :1 ⁇ 1:10.
- the ratio of the average daily dose of the compound of formula I or its pharmaceutically acceptable salt to entecavir or its pharmaceutically acceptable salt or solvate is selected from 10:1, 9:1 , 8:1, 7:1, 6:1, 5:1, 4:1, 3:1, 2:1, 1:1, 1:1.1, 1:1.2, 1:1.3, 1:1.4, 1 :1.5, 1:1.6, 1:1.7, 1:1.8, 1:1.9, 1:2, 1:2.1, 1:2.2, 1:2.3, 1:2.4, 1:2.5, 1:2.6, 1:2.7 , 1:2.8, 1:2.9, 1:3, 1:3.1, 1:3.2, 1:3.3, 1:3.4, 1:3.5, 1:3.6, 1:3.7, 1:3.8, 1:3.9, 1 :4, 1:4.1, 1:4.2, 1:4.3, 1:4.4, 1:4.5, 1:4.6, 1:4.7, 1:4.8, 1:4.9, 1:5, 1:5.1, 1:5.2 , 1:5.3, 1:5.4, 1:5.5, 1:5.6, 1:5.7, 1:
- the ratio of the average daily dose of the compound of formula I or its pharmaceutically acceptable salt to entecavir or its pharmaceutically acceptable salt or solvate (in units of weight) is preferably from 1:1.5 to 1:4 , 1:1.6 ⁇ 1:3.8, 1:1.8 ⁇ 1:3.8, 1:1.8 ⁇ 1:3.6 or 1:2 ⁇ 1:3.5.
- the drug combination is a fixed combination.
- the fixed combination is in the form of a solid pharmaceutical composition.
- the compound of formula I or its pharmaceutically acceptable salt and entecavir or its pharmaceutically acceptable salt or solvate in the fixed combination are present in the same solid pharmaceutical composition.
- the drug combination is a non-fixed combination.
- the compound of formula I or its pharmaceutically acceptable salt and entecavir or its pharmaceutically acceptable salt or solvate in the non-fixed combination are each in the form of a solid pharmaceutical composition.
- the compound of formula I or its pharmaceutically acceptable salt and entecavir or its pharmaceutically acceptable salt or solvate in the non-fixed combination are each in the form of a solid pharmaceutical composition, and the compound of formula I or its The solid pharmaceutical composition of the pharmaceutically acceptable salt and the solid pharmaceutical composition of entecavir or its pharmaceutically acceptable salt or solvate exist in the same medicine bag.
- the compound of formula I or its pharmaceutically acceptable salt and entecavir or its pharmaceutically acceptable salt or solvate in the non-fixed combination are each in the form of a solid pharmaceutical composition, and the compound of formula I or its The solid pharmaceutical composition of pharmaceutically acceptable salt and the solid pharmaceutical composition of entecavir or its pharmaceutically acceptable salt or solvate do not exist in the same bag.
- the solid pharmaceutical composition is selected from tablets or capsules.
- the application also provides the use of the drug combination of the application in the preparation of a medicament for the treatment of hepatitis B virus infection.
- the drug combination is as described above.
- this application also provides a method for treating hepatitis B virus infection, which comprises administering an effective amount of the drug combination of the application to an individual in need.
- the drug combination is as described above.
- the present application also provides the drug combination of the present application for the treatment of hepatitis B virus infection.
- the drug combination is as described above.
- the application also provides the use of the drug combination of the application for the treatment of hepatitis B virus infection.
- the drug combination is as described above.
- the application provides the use of a compound of formula I or a pharmaceutically acceptable salt thereof and entecavir or a pharmaceutically acceptable salt or solvate thereof in the preparation of a medicament for the treatment of hepatitis B virus infection , wherein the compound of formula I or its pharmaceutically acceptable salt and entecavir or its pharmaceutically acceptable salt or solvate are respectively prepared into pharmaceutical compositions.
- the present application also provides a kit for treating hepatitis B virus infection, which comprises: (a) a first compound containing a compound of formula I or a pharmaceutically acceptable salt thereof as an active ingredient; A pharmaceutical composition; and (b) a second pharmaceutical composition containing entecavir or a solvate thereof as an active ingredient; and optionally (c) a compound of formula I or a pharmaceutically acceptable salt thereof and entecavir or a solvate thereof Instructions for the combined use of medicinal salts and solvates.
- the compound of formula I or a pharmaceutically acceptable salt thereof is selected from a compound of formula A or a pharmaceutically acceptable salt thereof:
- the compound of formula A belongs to the prior art, and its chemical name is 2-butoxy-7-(4-(pyrrolidin-1-ylmethyl)benzyl)-5H-pyrrolo[3,2-d] Pyrimidine-4-amine, its preparation method and chemical properties can refer to WO2016023511.
- the pharmaceutically acceptable salt of the compound of formula A is selected from maleate or fumarate.
- the pharmaceutical composition of the compound of formula A or a pharmaceutically acceptable salt thereof is selected from solid pharmaceutical compositions, preferably from tablets or capsules.
- the compound of formula A or a pharmaceutically acceptable salt thereof is in the form of a pharmaceutical composition
- the pharmaceutical composition is a pharmaceutical composition with a single dose of 0.01 mg to 10 mg, preferably from a single dose of 0.01 mg, 0.02mg, 0.05mg, 0.08mg, 0.1mg, 0.2mg, 0.3mg, 0.4mg, 0.5mg, 0.6mg, 0.7mg, 0.8mg, 0.9mg, 1.0mg, 1.1mg, 1.2mg, 1.3mg, 1.4mg , 1.5mg, 1.6mg, 1.7mg, 1.8mg, 1.9mg, 2.0mg, 2.1mg, 2.2mg, 2.3mg, 2.4mg, 2.5mg, 2.6mg, 2.7mg, 2.8mg, 2.9mg, 3.0mg, 3.1 mg, 3.2mg, 3.3mg, 3.4mg, 3.5mg, 3.6mg,
- Entecavir 2-amino-9-[(1S,3R,4S)-4-hydroxy-3-hydroxymethyl-2-methylenecyclopentyl]-1,9- Dihydro-6H-purin-6-one, which has the following structural formula:
- the entecavir includes its pharmaceutically acceptable salt, and the pharmaceutically acceptable salt is selected from the maleate salt. In some of the schemes, the pharmaceutically acceptable salt of Entecavir is selected from monomaleate.
- the entecavir includes its solvate, and the solvate is selected from entecavir hydrate. In some of the schemes, the entecavir hydrate is selected from entecavir 0.5-2 hydrate. In some of the schemes, the entecavir hydrate is selected from entecavir monohydrate.
- the entecavir is selected from entecavir-maleate, entecavir monohydrate, or entecavir-maleate monohydrate.
- entecavir or a pharmaceutically acceptable salt or solvate thereof is in the form of a pharmaceutical composition.
- the pharmaceutical composition is selected from solid pharmaceutical compositions.
- the solid pharmaceutical composition is preferably selected from tablets or capsules.
- the pharmaceutical composition of entecavir or its pharmaceutically acceptable salts or solvates is selected from pharmaceutical compositions with a single dose of 0.01 mg to 5 mg, preferably from a single dose of 0.01 mg, 0.02 mg, and 0.05 mg.
- the entecavir or its pharmaceutically acceptable salt, its solvate, or its pharmaceutical composition can be selected from commercially available products.
- the compound of formula I or a pharmaceutically acceptable salt thereof is a TLR7 agonist.
- Entecavir 2-amino-9-[(1S,3R,4S)-4-hydroxy-3-hydroxymethyl-2-methylenecyclopentyl]-1,9- Dihydro-6H-purin-6-one, which has the following structural formula:
- the compound of formula I includes its non-salt form (for example, free acid or free base), as well as its pharmaceutically acceptable salt, and the non-salt or salt is included in the protection scope of this application.
- the pharmaceutically acceptable salt of the compound of formula I may be hydrochloride, maleate or fumarate.
- the entecavir includes its unsolvated form and also its solvated form, and the unsolvated or solvate is included in the scope of protection of the present application.
- the ratio of the amount of the compound to the solvent substance can be selected from the range of 1:0.5, 1:1, 1:1.5, 1:2 or any endpoint, such as 1:0.5 to 1:2 , 1:0.5 ⁇ 1:1.5, or 1:1 ⁇ 1:1.5.
- the entecavir is in an unsolvated form.
- the entecavir is in the form of a hydrate.
- the entecavir is in the form of a monohydrate.
- the dosage is calculated based on the weight of the compound in its free form, which refers to non-salt compounds and non-solvates.
- substituted or “substituted” means that any one or more hydrogen atoms on a specific atom is replaced by a substituent, as long as the valence of the specific atom is normal and the substituted compound is stable.
- the term “optional” or “optionally” means that the event or situation described later can occur or not occur, and the description includes occurrence of said event or situation and non-occurrence of said event or situation.
- the ethyl group is "optionally" substituted by halogen, meaning that the ethyl group can be unsubstituted (CH 2 CH 3 ), monosubstituted (such as CH 2 CH 2 F), or polysubstituted (such as CHFCH 2 F, CH 2 CHF 2 etc.) or completely substituted (CF 2 CF 3 ).
- CH 2 CH 3 unsubstituted
- monosubstituted such as CH 2 CH 2 F
- polysubstituted such as CHFCH 2 F, CH 2 CHF 2 etc.
- CF 2 CF 3 completely substituted
- C mn in this context means that the part has an integer number of carbon atoms in a given range.
- C 1-6 means that the group can have 1 carbon atom, 2 carbon atoms, 3 carbon atoms, 4 carbon atoms, 5 carbon atoms, or 6 carbon atoms.
- any variable such as R
- its definition in each case is independent. So, for example, if a group is replaced by 2 Rs, then each R has independent options.
- linking group When the number of a linking group is 0, such as -(CH 2 ) 0 -, it means that the linking group is a covalent bond.
- the substituent can be bonded to any atom on the ring.
- the structural unit It means that it can be substituted at any position on the cyclohexyl or cyclohexadiene.
- halo or halogen refers to fluorine, chlorine, bromine and iodine.
- hydroxy refers to the -OH group.
- cyano refers to the -CN group.
- mercapto refers to the -SH group.
- amino refers to the -NH 2 group.
- alkyl refers to a hydrocarbon group of the general formula C n H 2n+1.
- the alkyl group may be linear or branched.
- C 1 - 6 alkyl refers to (e.g., methyl, ethyl, n-propyl, isopropyl, alkyl containing 1 to 6 carbon atoms, n-butyl, isobutyl, sec-butyl, Tert-butyl, n-pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, neopentyl, hexyl, 2-methylpentyl, etc.).
- alkyl moiety (ie, alkyl) of alkoxy, monoalkylamino, dialkylamino, alkylsulfonyl, and alkylthio have the same definition as described above.
- alkoxy refers to -O-alkyl
- cycloalkyl refers to a carbocyclic ring that is fully saturated and may exist as a monocyclic, bridged, or spiro ring. Unless otherwise indicated, the carbocyclic ring is usually a 3- to 10-membered ring.
- Non-limiting examples of cycloalkyl groups include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, norbornyl (bicyclo[2.2.1]heptyl), bicyclo[2.2.2]octyl, diamond Alkyl and so on.
- cyclic hydrocarbon group refers to a saturated or unsaturated non-aromatic cyclic hydrocarbon group composed of carbon atoms and hydrogen atoms, and preferably contains one or two rings.
- the cyclic hydrocarbon group may be a monocyclic ring, a fused polycyclic ring, a bridged ring or a spiro ring structure.
- Non-limiting examples of cycloalkyl include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, bicyclo[2.2.1]heptyl, spiro[3.3]heptyl, and the like.
- heterocyclyl refers to a non-aromatic ring that is fully saturated or partially unsaturated (but not fully unsaturated heteroaromatic) and may exist as a single ring, bridged ring, or spiro ring.
- the heterocyclic ring is generally a 3 to 7 membered ring containing 1 to 3 heteroatoms (preferably 1 or 2 heteroatoms) independently selected from sulfur, oxygen, and/or nitrogen.
- heterocyclic groups include, but are not limited to, oxiranyl, tetrahydrofuryl, dihydrofuranyl, pyrrolidinyl, N-methylpyrrolidinyl, dihydropyrrolyl, piperidinyl, piperazinyl , Pyrazolidinyl, 4H-pyranyl, morpholinyl, thiomorpholinyl, tetrahydrothienyl, etc.
- heterocycloalkyl refers to a cyclic group that is fully saturated and may exist as a monocyclic, bridged, or spiro ring. Unless otherwise indicated, the heterocyclic ring is generally a 3 to 7 membered ring containing 1 to 3 heteroatoms (preferably 1 or 2 heteroatoms) independently selected from sulfur, oxygen, and/or nitrogen.
- 3-membered heterocycloalkyl groups include, but are not limited to, oxirane, sulfidene, and azaethylenyl groups
- 4-membered heterocycloalkyl groups include, but are not limited to, azetidinyl, oxetane
- Examples of cyclic group, thiabutanyl, 5-membered heterocycloalkyl include but are not limited to tetrahydrofuranyl, tetrahydrothienyl, pyrrolidinyl, isoxazolidinyl, oxazolidinyl, isothiazolidinyl, thiazolidine
- 6-membered heterocycloalkyl groups include but are not limited to piperidinyl, tetrahydropyranyl, tetrahydrothiopyranyl, morpholinyl, piperazinyl, 1, Examples of 4-thiaxanyl, 1,4-dioxanyl, 1,4
- heterocyclic hydrocarbon group refers to a monocyclic, fused polycyclic, bridged ring or spiro ring system group without aromaticity, in which part of the ring atoms are selected from N, O, S(O) n (where n is 0 , 1 or 2), the remaining ring atoms are C.
- Such rings may be saturated or unsaturated (e.g., have one or more double bonds), but do not have a fully conjugated ⁇ -electron system.
- 3-membered heterocyclic hydrocarbyl groups include, but are not limited to, oxirane, sulfidene, and azidine groups.
- Examples of 4-membered heterocyclic hydrocarbyl groups include, but are not limited to, azetidinyl, oxbutanyl, and thiobutane.
- Cyclic groups, examples of 5-membered heterocyclic hydrocarbon groups include, but are not limited to, tetrahydrofuranyl, tetrahydrothienyl, pyrrolidinyl, isoxazolidinyl, oxazolidinyl, isothiazolidinyl, 1,1-dioxoisopropyl
- Examples of thiazolidinyl, thiazolidinyl, imidazolidinyl, tetrahydropyrazolyl, pyrrolinyl, dihydrofuranyl, dihydrothienyl, and 6-membered heterocyclic hydrocarbon groups include, but are not limited to, piperidinyl, tetrahydropyridine Pyranyl, tetrahydrothiopyranyl,
- aryl refers to an all-carbon monocyclic or fused polycyclic aromatic ring group having a conjugated ⁇ -electron system.
- the aryl group can have 6-20 carbon atoms, 6-14 carbon atoms, or 6-12 carbon atoms.
- Non-limiting examples of aryl groups include, but are not limited to, phenyl, naphthyl, anthracenyl, 1,2,3,4-tetralin and the like.
- heteroaryl refers to a monocyclic or condensed polycyclic ring system, which contains at least one ring atom selected from N, O, and S, the remaining ring atoms are C, and have at least one aromatic ring.
- Preferred heteroaryl groups have a single 5- to 8-membered ring, or multiple fused rings containing 6 to 14, especially 6 to 10 ring atoms.
- heteroaryl groups include, but are not limited to, pyrrolyl, furyl, thienyl, imidazolyl, oxazolyl, pyrazolyl, pyridyl, pyrimidinyl, pyrazinyl, quinolinyl, isoquinolinyl , Tetrazolyl, triazolyl, triazinyl, benzofuranyl, benzothienyl, indolyl, isoindolyl, etc.
- the compounds of the present application may be asymmetric, for example, have one or more stereoisomers. Unless otherwise specified, all stereoisomers include, for example, enantiomers and diastereomers.
- the compounds of the present application containing asymmetric carbon atoms can be isolated in an optically pure form or in a racemic form. The optically active pure form can be resolved from the racemic mixture or synthesized by using chiral raw materials or chiral reagents.
- administering refers to the physical introduction of a composition containing a therapeutic agent to a subject using any of a variety of methods and delivery systems known to those skilled in the art.
- treatment generally refers to obtaining a desired pharmacological and/or physiological effect.
- the effect can be therapeutic based on partial or complete stabilization or cure of the disease and/or side effects due to the disease.
- Treatment encompasses any treatment of a patient's disease, including: (a) inhibiting the symptoms of the disease, that is, preventing its development; or (b) alleviating the symptoms of the disease, that is, causing the disease or symptoms to degenerate.
- the term "effective amount” means (i) treatment or prevention of a specific disease, condition or disorder, (ii) reduction, amelioration or elimination of one or more symptoms of a specific disease, condition or disorder, or (iii) prevention or delay herein
- the amount of the compound of the present application that constitutes a “therapeutically effective amount” varies depending on the compound, the disease state and its severity, the mode of administration, and the age of the mammal to be treated, but it can be routinely determined by those skilled in the art. Determined by its own knowledge and this disclosure.
- the term "individual" may be a mammal. In some embodiments, the subject is a mouse. In some embodiments, the subject is a human.
- the compound of formula I or a pharmaceutically acceptable salt thereof can be administered by any suitable route and method, for example, oral or parenteral (for example, intravenous) administration.
- the therapeutically effective amount of the compound of formula I or a pharmaceutically acceptable salt thereof includes, but is not limited to, from about 0.0001 to 20 mg/kg weight/day, for example, from 0.001 to 10 mg/kg weight/day.
- the dosage frequency of the compound of formula I or its pharmaceutically acceptable salt is determined by the needs of the individual patient, including the severity, disease response, any treatment-related toxicity, the patient’s age and health status, for example, once or twice a day, Or more times a day.
- the administration may be intermittent, for example, where the subject receives a daily dose of the compound of formula I or a pharmaceutically acceptable salt thereof during a period of several days, and then during a period of several days or more, the patient does not Receive a daily dose of a compound of formula I or a pharmaceutically acceptable salt thereof.
- Entecavir can be administered by a variety of routes, including but not limited to oral, parenteral, intraperitoneal, intravenous, intraarterial, transdermal, sublingual, intramuscular, rectal, transbuccal, intranasal, inhalation, vaginal , Intraocular, topical administration, subcutaneous, intra-fat, intra-articular, intraperitoneal and intrathecal. In some specific embodiments, it is administered orally. The amount of entecavir administered can be determined based on the severity of the disease, the response of the disease, any treatment-related toxicity, the age and health of the patient. For example, the daily dose of entecavir administered can be 0.005 mg to 10.0 mg. Entecavir can be administered one or more times a day. In some embodiments, Entecavir is administered as an oral solid formulation once a day.
- drug combination refers to the simultaneous, concurrent or sequential use of two or more active ingredients.
- fixed combination means that the active ingredients (such as TLR7 agonists or entecavir) are administered to a subject simultaneously in a fixed total dose or dose ratio, or in the form of a single entity, pharmaceutical composition or preparation. In some embodiments, for example, in the same tablet or the same capsule or the same drug bag.
- active ingredients such as TLR7 agonists or entecavir
- non-fixed combination refers to two or more active ingredients as independent entities (such as pharmaceutical compositions, pharmaceutical preparations) administered to an individual at the same time, concurrently or sequentially without any specific time limit, wherein the active ingredients administered to the individual reach The therapeutically effective dose level.
- An example of a non-fixed combination is cocktail therapy, such as the administration of two, three or more active ingredients.
- the respective active components can be packaged, sold or administered as completely independent pharmaceutical compositions.
- the "non-fixed combination” also includes the combined use of the "fixed combination” or the "fixed combination” with any one or more independent entities of the active ingredient.
- pharmaceutical composition refers to a mixture of one or more of the compounds of the application or their pharmaceutical combinations or their salts and pharmaceutically acceptable excipients.
- the purpose of the pharmaceutical composition is to facilitate the administration of the compound of the present application or its pharmaceutical combination to a subject.
- pharmaceutically acceptable refers to those compounds, materials, compositions and/or dosage forms that are within the scope of reliable medical judgment and are suitable for use in contact with human and animal tissues without excessive Toxicity, irritation, allergic reactions or other problems or complications of the disease are commensurate with a reasonable benefit/risk ratio.
- pharmaceutically acceptable salt or “pharmaceutically acceptable salt” refers to a salt of the compound of the present application within the definition of “pharmaceutically acceptable”.
- the active ingredients in the pharmaceutical combination of the present application can be formulated separately, or part or all of them can be formulated together.
- the pharmaceutical combination of the present application can be formulated into a pharmaceutical composition suitable for single or multiple administration.
- the active components in the pharmaceutical combination of the present application can be administered individually, or part or all of them can be administered together.
- the components of the pharmaceutical combination of the present application may be administered at substantially different times, or some or all of them may be administered at substantially the same time.
- the active ingredients in the pharmaceutical combination of the present application can be administered independently, or part or all of them can be administered by various suitable routes, including but not limited to oral or parenteral (by intravenous, intramuscular, topical or subcutaneous routes). ).
- the active components of the pharmaceutical combination of the present application may each independently, or part or all of them are jointly administered orally or by injection, such as intravenous injection or intraperitoneal injection.
- the active components in the pharmaceutical combination of the present application may be independently, or some or all of them may be a suitable dosage form together, including but not limited to: tablets, troches, pills, capsules (such as hard capsules, soft capsules, Enteric-coated capsules, microcapsules), elixirs, granules, syrups, injections (intramuscular, intravenous, intraperitoneal), powders, emulsions, suspensions, solutions, dispersions and for oral or non-oral administration
- suitable dosage form including but not limited to: tablets, troches, pills, capsules (such as hard capsules, soft capsules, Enteric-coated capsules, microcapsules), elixirs, granules, syrups, injections (intramuscular, intravenous, intraperitoneal), powders, emulsions, suspensions, solutions, dispersions and for oral or non-oral administration
- suitable dosage form including but not limited to: tablets, troches, pills, capsules (such as hard capsule
- the active components in the pharmaceutical combination of the present application may each independently, or part or all of them together contain pharmaceutically acceptable carriers and/or excipients.
- the pharmaceutical combination of the present application may also include additional therapeutic agents.
- the additional therapeutic agent may be a therapeutic agent known in the art to treat hepatitis B virus infection.
- an effective amount of the compound of formula I of the present application or a pharmaceutically acceptable salt thereof and entecavir or a pharmaceutically acceptable salt or solvate thereof can be administered to an individual in need at the same time, sequentially or at intervals.
- an effective amount of the compound of formula I or a pharmaceutically acceptable salt thereof and entecavir or a pharmaceutically acceptable salt or a solvate thereof can be administered to an individual in need in the same or different dosage regimen.
- the compound of formula I or a pharmaceutically acceptable salt thereof is administered three times a day, twice a day, once every day, once every two days, once every three days, once every four days, Administer once every five days, once every six days, once every week, once every two weeks, or once every three weeks.
- the compound of formula I or a pharmaceutically acceptable salt thereof is administered at a dose of 0.1 to 10.0 mg, preferably 0.1 mg, 0.2 mg, 0.3 mg, 0.4 mg, 0.5 mg, 0.6 mg, 0.7 mg, 0.8mg, 0.9mg, 1.0mg, 1.1mg, 1.2mg, 1.3mg, 1.4mg, 1.5mg, 1.6mg, 1.7mg, 1.8mg, 1.9mg, 2.0mg, 2.1mg, 2.2mg, 2.3mg, 2.4mg , 2.5mg, 2.6mg, 2.7mg, 2.8mg, 2.9mg, 3.0mg, 3.1mg, 3.2mg, 3.3mg, 3.4mg, 3.5mg, 3.6mg, 3.7mg, 3.8mg, 3.9mg, 4.0mg, 4.1 mg, 4.2mg, 4.3mg, 4.4mg, 4.5mg, 4.6mg, 4.7
- the compound of formula I or a pharmaceutically acceptable salt thereof is administered 0.2 to 5.0 mg, 0.4 to 4.0 mg, 0.5 to 3.0 mg, 0.6 to 2.6 mg, 0.8 to 2.2 mg, 0.8 to 1.8 mg each time , 1.0 to 2.0 mg, 1.0 to 1.8 mg, or 1.0 to 1.6 mg dose.
- the compound of formula I or a pharmaceutically acceptable salt thereof is administered once a week, and each administration is 0.2 to 5.0 mg, 0.4 to 4.0 mg, 0.5 to 3.0 mg, 0.6 to 2.6 mg, 0.8 to 2.2 mg , 0.8 to 1.8 mg, 1.0 to 2.0 mg, 1.0 to 1.8 mg, or 1.0 to 1.6 mg.
- the compound of formula I or a pharmaceutically acceptable salt thereof is administered once a week, with a dose of 1.0 to 1.8 mg each time.
- the entecavir or its pharmaceutically acceptable salt, its solvate is administered three times a day, twice a day, once a day, once every two days, once every three days, and once every four days.
- the entecavir or its pharmaceutically acceptable salt or solvate is administered at a dose of 0.005 mg to 5.0 mg each time, preferably 0.01 mg, 0.05 mg, 0.1 mg, 0.2 mg, 0.3 mg, 0.4 mg, 0.5 mg, 0.6mg, 0.7mg, 0.8mg, 0.9mg, 1.0mg, 1.1mg, 1.2mg, 1.3mg, 1.4mg, 1.5mg, 1.6mg, 1.7mg, 1.8mg, 1.9mg, 2.0mg, 2.1mg, 2.2mg, 2.3mg, 2.4mg, 2.5mg, 2.6mg, 2.7mg, 2.8mg, 2.9mg, 3.0mg, 3.1mg, 3.2mg, 3.3mg, 3.4mg, 3.5mg, 3.6mg, 3.7mg, 3.8mg , 3.9 mg, 4.0 mg, 4.1 mg, 4.2 mg, 4.3 mg, 4.4 mg
- the entecavir or a pharmaceutically acceptable salt or solvate thereof is administered once a day, with a dose of 0.10 mg to 2.0 mg each time.
- the entecavir or its pharmaceutically acceptable salt or solvate can be administered once a day, with a dose of 0.5 mg each time.
- the TLR7 agonist ie, the compound of formula I
- the entecavir is administered once a day with a dose of 0.5 mg each time.
- the drug combination of the present application can significantly reduce the HBV DNA level or alleviate other HBV indicators; and compared with a single drug, the drug combination of the present application shows a significant enhancement effect. It shows that the drug combination of the present application has good medicinal value.
- FIG. 1 The effect of TLR7 agonist on the level of serum HBV DNA replication in AAV mice.
- the TLR7 agonist is (2-Butoxy-7-(4-(pyrrolidin-1-ylmethyl)benzyl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine), the preparation method can be referred to WO2016023511.
- entecavir is used as its monohydrate.
- mice were randomly grouped according to the number of HBV DNA copies, with vehicle control group, TLR7 agonist group (20mg/kg, tiw), and entecavir (ETV) group (0.0032 (1st week, 1W) & 0.001 (2-6 weeks) , 2-6W) mg/kg, qd), TLR7 agonist combined with ETV group, 6 mice in each group. Each group of mice was given intragastric administration for 6 weeks, and the drug was stopped for 3 weeks.
- TLR7 agonist group 20mg/kg, tiw
- ETV entecavir
- Jin Zhengjun is based on Burgi’s formula method, which analyzes its shortcomings and makes corrections. It is also called probability addition method:
- E A represents the effect of drug A alone
- E B represents the effect of drug B alone
- E A+B represents the effect of the combination of two drugs A and B.
- q value 0.85 ⁇ 1.15 is simple addition; greater than 1.15 ⁇ 20 is enhancement; greater than 20 is significant increase; less than 0.85 ⁇ 0.55 is antagonism; less than 0.55 is significant antagonism.
- the q value is taken as an absolute value.
- the TLR7 agonist is (2-Butoxy-7-(4-(pyrrolidin-1-ylmethyl)benzyl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine), the preparation method can be referred to WO2016023511. Prepare it into 0.2mg/tablet or 0.5mg/tablet size tablets for later use.
- Entecavir Commercially available Entecavir tablets, the specification is 0.5mg/tablet.
- Commercially available entecavir tablets include but are not limited to entecavir dispersible tablets (runzhong ).
- Placebo A placebo of TLR7 agonists.
- Serum virological criteria Serum HBsAg positive for more than 6 months or evidence of chronic hepatitis B for 6 months.
- HBV DNA suppression the lower limit of normal detection, and the detection of HBV DNA suppression using Roche reagent during the screening period is defined as ⁇ 69IU/mL; Fibroscan ⁇ 9.0Kpa (fasting), ALT ⁇ 5 ⁇ ULN .
- Newly treated patients HBeAg-positive chronic hepatitis B patients, HBV DNA>10 5 copies/mL (or>20000IU/mL), or HBeAg-negative patients HBV DNA>10 4 copies/mL (or>2000IU/mL), use Roche
- the second-generation Cobas Taqman real-time quantitative PCR method is used for detection, and the detection limit is 20IU/mL; Fibroscan ⁇ 12.4Kpa (fasting), 1 ⁇ ULN ⁇ ALT ⁇ 5 ⁇ ULN.
- the newly-treated patients refer to those who have never received HBV antiviral treatment or participated in relevant clinical trials.
- TLR7 agonist Administer once a week.
- Entecavir The dosage is 0.5 mg/day, once a day.
- the first group consisted of 12 subjects, of which 8 took 1.2 mg TLR7 agonist combined with entecavir, and 4 took placebo combined with entecavir for a total of 24 weeks.
- Each dose group took the medicine for 24 weeks.
- Curative effect indicators serum HBsAg, HBeAg, or HBV DNA, etc.
- the mean, standard deviation, median, quartile, minimum and maximum value of the average content of the index parameters at each detection time point in each group and the description of the change from the baseline were used; the repeated measures mixed effects model (MMRM) ), the group, the baseline value, the detection time point, and the interaction terms between the group and the detection time point are regarded as fixed effects, and the subjects and intercept terms are regarded as random effects.
- the change from baseline was compared with the placebo group and adjusted by Dunnett's method.
- TLR7 agonists combined with Entecavir significantly inhibited HBV DNA replication in patients.
- the combined administration group of TLR7 agonist and placebo achieved inhibition of HBV DNA replication.
- the combined administration group of entecavir and placebo also has an inhibitory effect on HBV DNA replication.
Abstract
Description
Claims (15)
- 药物组合,其包括式I化合物或其药学上可接受的盐和恩替卡韦或其可药用盐、溶剂合物,所述式I化合物如下所示:其中,L 1选自-O-;L 2选自-CH 2-,其中上述-CH 2-任选被R 4取代;R 1选自氢、或C 1-10烷基,其中上述C 1-10烷基任选被R 5取代;R 2选自氢、氰基、-COOH、或-CONH 2,其中上述-COOH、和-CONH 2任选被R 6取代;B选自6-10元芳基、或5-10元杂芳基;L 3选自C 0-6亚烷基、或亚氨基,其中上述C 0-6亚烷基、和亚氨基任选被R 7取代;R 3选自氢、氨基、C 1-10烷基、C 3-10环烃基、3-10元杂环烃基、6-10元芳基、或5-10元杂芳基,其中上述氨基、C 1-10烷基、C 3-10环烃基、3-10元杂环烃基、6-10元芳基、或5-10元杂芳基任选被R 8取代,或者,R 3和L 3与B环上邻位原子一起形成饱和或不饱和的5-8元环,所述5-8元环任选被R 9取代;n为0、1、2、3、4或5;R 4、R 5、R 6、R 7、R 8、和R 9各自独立地选自卤素、氰基、羟基、巯基、氨基、-R、-OR、=O、-SR、-NHR、-NR 2;R独立地选自C 1-8烷基、C 3-8环烃基、3-8元杂环烃基、6-8元芳基、5-8元杂芳基。
- 如权利要求1所述的药物组合,其特征在于,所述式I化合物或其药学上可接受的盐选自:2-丁氧基-7-(3-((4-甲基哌嗪-1-基)甲基)苄基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-(3-(吗啉代甲基)苄基)-5H-吡咯并[3,2-d]嘧啶-4-胺;7-(3-(氨基甲基)苄基)-2-丁氧基-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-(3-(吡咯烷-1-基甲基)苄基)-5H-吡咯并[3,2-d]嘧啶-4胺;2-丁氧基-7-(4-((3,3-二氟吡咯烷-1-基)甲基)苄基-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-(4-((3-氟吡咯烷-1-基)甲基)苄基)-5H-吡咯并[3,2-d]嘧啶-4-胺;1-(4-((4-氨基-2-丁氧基-5H-吡咯并[3,2-d]嘧啶-7-基)甲基)苄基)吡咯烷-3-醇;2-丁氧基-7-(4-(哌啶-1-基甲基)苄基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-(4-(吗啉代甲基)苄基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-(4-((4-甲基哌嗪-1-基)甲基)苄基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-(4-((二甲基氨基)甲基)苄基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-(4-((二乙基氨基)甲基)苄基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-(4-((二丙基氨基)甲基)苄基)-5H-吡咯并[3,2-d]嘧啶-4-胺;7-(4-(氮杂环丁烷-1-基甲基)苄基)-2-丁氧基-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-(4-((3-甲氧基氮杂环丁烷-1-基)甲基)苄基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-(4-((4-甲基-1,4-二氮杂环庚烷-1-基)甲基)苄基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-(4-((2,6-二甲基吗啉基)甲基)苄基)-5H-吡咯并[3,2-d]嘧啶-4-胺;7-(4-((1S,4S)-2-氧杂-5-氮杂双环[2.2.1]庚烷-5-基甲基)苄基)-2-丁氧基-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-(4-((4-甲氧基哌啶-1-基)甲基)苄基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-(4-((4-异丙基哌嗪-1-基)甲基)苄基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-(4-(吡咯烷-1-基甲基)苄基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-((6-(吡咯烷-1-基甲基)吡啶-3-基)甲基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-(3-(2-(吡咯烷-1-基)乙基)苄基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-(4-(1-(吡咯烷-1-基)乙基)苄基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-(4-(1-甲基哌啶-4-基)苄基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-(4-(1-甲基吡咯烷-2-基)苄基)-5H-吡咯并[3,2-d]嘧啶-4-胺;1-(4-((4-氨基-2-丁氧基-5H-吡咯并[3,2-d]嘧啶-7-基)甲基)苯基)-4-甲基哌嗪-2-酮;7-苄基-2-(2-甲氧基乙氧基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-(2-甲氧基乙氧基)-7-((6-甲基吡啶-3-基)甲基)-5H-吡咯并[3,2-d]嘧啶-4-胺;7-((5-氯吡啶-2-基)甲基)-2-(2-甲氧基乙氧基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-(2-甲氧基乙氧基-)-7-((6-(吡咯烷-1-基甲基)吡啶-3-基)甲基)-5H-吡咯并[3,2-d]嘧啶-4-胺;1-(4-((4-氨基-2-(2-甲氧基乙氧基)-5H-吡咯并[3,2-d]嘧啶-7-基)甲基)苯基)-4-甲基哌嗪-2-酮;2-丁氧基-7-((5-(吡咯烷-1-基甲基)吡啶-2-基)甲基)-5H-吡咯并[3,2-d]嘧啶-4-胺;4-氨基-2-丁氧基-7-((6-(吡咯烷-1-基甲基)吡啶-3-基)甲基)-5H-吡咯并[3,2-d]嘧啶-6-甲腈;4-氨基-2-丁氧基-7-(4-(吡咯烷-1-基甲基)苄基)-5H-吡咯并[3,2-d]嘧啶-6-甲腈;4-氨基-2-丁氧基-7-(4-(吗啉代甲基)苄基)-5H-吡咯并[3,2-d]嘧啶-6-甲腈;4-氨基-2-丁氧基-7-(4-((4-甲基哌嗪-1-基)甲基)苄基)-5H-吡咯并[3,2-d]嘧啶-6-甲腈;4-氨基-2-丁氧基-7-(4-(吡咯烷-1-基甲基)苄基)-5H-吡咯并[3,2-d]嘧啶-6-甲酰胺;2-丁氧基-7-((1,2,3,4-四氢异喹啉-7-基)甲基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-((2-甲基-1,2,3,4-四氢异喹啉-7-基)甲基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-((2-乙基-1,2,3,4-四氢异喹啉-7-基)甲基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-((2-异丙基-1,2,3,4-四氢异喹啉-7-基)甲基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-((1,2,3,4-四氢异喹啉-6-基)甲基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-((2-甲基-1,2,3,4-四氢异喹啉-6-基)甲基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-((2-乙基-1,2,3,4-四氢异喹啉-6-基)甲基)-5H-吡咯并[3,2-d]嘧啶-4-胺;2-丁氧基-7-((2-(吡咯烷-1-基甲基)噻唑-5-基)甲基)-5H-吡咯并[3,2-d]嘧啶-4-胺或其药学上可接受的盐。
- 如权利要求1所述的药物组合,其特征在于,所述恩替卡韦或其可药用盐、溶剂合物选自恩替卡韦马来酸盐、恩替卡韦一马来酸盐、恩替卡韦水合物、恩替卡韦0.5~2水合物、或恩替卡韦一水合物;任选地,所述恩替卡韦或其可药用盐、溶剂合物选自恩替卡韦一马来酸盐一水合物。
- 如权利要求1~4任一项所述的药物组合,其特征在于,所述药物组合中式I化合物或其药学上可接受的盐与恩替卡韦或其可药用盐、溶剂合物的平均日剂量之比选自10:1~1:10;任选地,所述平均日剂量之比选自1:1.5~1:4、1:1.6~1:3.8、1:1.8~1:3.8、1:1.8~1:3.6或1:2~1:3.5。
- 如权利要求1~5任一项所述的药物组合,其特征在于,所述药物组合的式I化合物或其药学上可接受的盐每一天施用三次、每一天施用两次、每一天施用一次、每两天施用一次、每三天施用一次、每四天施用一次、每五天施用一次,每六天施用一次、每一周施用一次、每两周施用一次、或每三周施用一次。
- 如权利要求1~6任一项所述的药物组合,其特征在于,所述药物组合的式I化合物或其药学上可接受的盐每一次施用0.1~10.0mg的剂量;任选地,所述式I化合物或其药学上可接受的盐每一次施用0.2至5.0mg、0.4至4.0mg、0.5至3.0mg、0.6至2.6mg、0.8至2.2mg、0.8至1.8mg、1.0至2.0mg、1.0至1.8mg、或1.0至1.6mg的剂量。
- 如权利要求1~7任一项所述的药物组合,其特征在于,所述药物组合的恩替卡韦或其可药用盐、溶剂合物每一天施用三次、每一天施用两次、每一天施用一次、或每两天施用一次,每三天施用一次、每四天施用一次、每五天施用一次、每六天施用一次、每一周施用一次、每两周施用一次、或每三周施用一次。
- 如权利要求1~8任一项所述的药物组合,其特征在于,所述药物组合的恩替卡韦或其可药用盐、溶剂合物每一次施用0.005mg至5.0mg的剂量;任选地,所述恩替卡韦或其可药用盐、溶剂合物每一次施用0.05mg至5.0mg、0.10mg至2.0mg、0.25mg至2.0mg、或0.5mg至1.0mg的剂量。
- 如权利要求1~9任一项所述的药物组合,其特征在于,所述药物组合是固定组合;任选地所述固定组合呈固体药物组合物形式;任选地,所述固定组合中的式I化合物或其药学上可接受的盐和恩替卡韦或其可药用盐、溶剂合物存在于同一固体药物组合物。
- 如权利要求1~9任一项所述的药物组合,其特征在于,所述药物组合是非固定组合;任选地,所述非固定组合中的式I化合物或其药学上可接受的盐和恩替卡韦或其可药用盐、溶剂合物各自呈固体药物组合物形式;任选地,所述非固定组合中的式I化合物或其药学上可接受的盐和恩替卡韦或其可药用盐、溶剂合物各自呈固体药物组合物形式,且式I化合物或其药学上可接受的盐的固体药物组合物和恩替卡韦或其可药用盐、溶剂合物的固体药物组合物存在于同一个药袋;任选地,所述非固定组合中的式I化合物或其药学上可接受的盐和恩替卡韦或其可药用盐、溶剂合物各自呈固体药物组合物形式,且式I化合物或其药学上可接受的盐的固体药物组合物和恩替卡韦或其可药用盐、溶剂合物的固体药物组合物不存在于同一个药袋。
- 如权利要求1~11任一项所述的药物组合在制备用于治疗乙型肝炎病毒感染的药物中的用途。
- 治疗乙型肝炎病毒感染的方法,其包括向有需要的个体施用有效量的如权利要求1~11任一项所述的药物组合。
- 用于治疗乙型肝炎病毒感染的药物组合,所述药物组合为选自如权利要求1~11任一项所述的药物组合。
- 权利要求1~11任一项所述的药物组合用于治疗乙型肝炎病毒感染的用途。
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102272134A (zh) * | 2008-12-09 | 2011-12-07 | 吉里德科学公司 | Toll样受体调节剂 |
WO2016023511A1 (zh) | 2014-08-15 | 2016-02-18 | 正大天晴药业集团股份有限公司 | 作为tlr7激动剂的吡咯并嘧啶化合物 |
CN105367576A (zh) * | 2014-08-15 | 2016-03-02 | 正大天晴药业集团股份有限公司 | 作为tlr7激动剂的吡咯并嘧啶化合物 |
WO2017076346A1 (zh) | 2015-11-05 | 2017-05-11 | 正大天晴药业集团股份有限公司 | 作为tlr7激动剂的7-(噻唑-5-基)吡咯并嘧啶化合物 |
WO2020188448A1 (en) * | 2019-03-15 | 2020-09-24 | Janssen Sciences Ireland Unlimited Company | Toll-like receptor agonists for use in the treatment of hepatitis b |
-
2020
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- 2020-09-29 AU AU2020355873A patent/AU2020355873A1/en active Pending
- 2020-09-29 CN CN202080066482.4A patent/CN114423433A/zh active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102272134A (zh) * | 2008-12-09 | 2011-12-07 | 吉里德科学公司 | Toll样受体调节剂 |
WO2016023511A1 (zh) | 2014-08-15 | 2016-02-18 | 正大天晴药业集团股份有限公司 | 作为tlr7激动剂的吡咯并嘧啶化合物 |
CN105367576A (zh) * | 2014-08-15 | 2016-03-02 | 正大天晴药业集团股份有限公司 | 作为tlr7激动剂的吡咯并嘧啶化合物 |
WO2017076346A1 (zh) | 2015-11-05 | 2017-05-11 | 正大天晴药业集团股份有限公司 | 作为tlr7激动剂的7-(噻唑-5-基)吡咯并嘧啶化合物 |
WO2020188448A1 (en) * | 2019-03-15 | 2020-09-24 | Janssen Sciences Ireland Unlimited Company | Toll-like receptor agonists for use in the treatment of hepatitis b |
Non-Patent Citations (3)
Title |
---|
ANONYMOUS: "A Study of TQ-A3334 Combined With Entecavir in the Treatment of Chronic Hepatitis B", CHIA TAI TIANQING PHARMACEUTICAL GROUP CO. LTD.; HTTPS://CLINICALTRIALS.GOV/CT2/SHOW/NCT04180150, 16 December 2019 (2019-12-16), XP055795262 * |
ANTONIO GONCALVES, ANNABELLE LEMENUEL-DIOT, LU GAO, LUE DAI, RUBEN ALVAREZ, JOSEPH GRIPPO, GUEDJ JEREMIE: "FRI-173-Modeling HBV kinetics in mice treated by a novel TLR7 agonist, alone or in combination with entecavir", JOURNAL OF HEPATOLOGY, ELSEVIER, AMSTERDAM, NL, vol. 70, no. 1, 1 April 2019 (2019-04-01), AMSTERDAM, NL, pages e465, XP055795256, ISSN: 0168-8278, DOI: 10.1016/S0618-8278(19)30918-1 * |
KOROLOWIZC KYLE E, LI BIN, HUANG XU, YON CHANGSUEK, RODRIGO EVELYN, CORPUZ MANNY, PLOUFFE DAVID M, KALLAKURY BHASKAR V, SURESH MAN: "Liver-Targeted Toll-Like Receptor 7 Agonist Combined With Entecavir Promotes a Functional Cure in the Woodchuck Model of Hepatitis B Virus", HEPATOLOGY COMMUNICATIONS, vol. 3, no. 10, 1 January 2019 (2019-01-01), pages 1296 - 1310, XP055795254, DOI: 10.1002/hep4.1397/suppinfo * |
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