AR059802A1 - Compuestos y derivados de dibencilamina, combinaciones y composiciones farmaceuticas que los comprenden y el uso de estos derivados en el tratamiento de enfermedades mediadas por la actividad de cetp. - Google Patents
Compuestos y derivados de dibencilamina, combinaciones y composiciones farmaceuticas que los comprenden y el uso de estos derivados en el tratamiento de enfermedades mediadas por la actividad de cetp.Info
- Publication number
- AR059802A1 AR059802A1 ARP070100979A ARP070100979A AR059802A1 AR 059802 A1 AR059802 A1 AR 059802A1 AR P070100979 A ARP070100979 A AR P070100979A AR P070100979 A ARP070100979 A AR P070100979A AR 059802 A1 AR059802 A1 AR 059802A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- groups
- halo
- cyano
- optionally substituted
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D257/04—Five-membered rings
- C07D257/06—Five-membered rings with nitrogen atoms directly attached to the ring carbon atom
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
- C07D453/06—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing isoquinuclidine ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Child & Adolescent Psychology (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Epidemiology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Compuestos de dibencilamina y derivados, composiciones farmacéuticas que contienen estos compuestos y el uso de estos compuestos para elevar los niveles plasmáticos de ciertos Iípidos, incluyendo el colesterol asociado a lipoproteínas de alta densidad y para reducir los niveles plasmáticos de otros lípidos, tales como el colesterol LDL y los triglicéridos y, por consiguiente, para tratar enfermedades que se exacerban por bajos niveles de colesterol-HDL y/o altos niveles de colesterol-LDL y triglicéridos, tales como aterosclerosis y enfermedades cardiovasculares en algunos mamíferos, incluyendo seres humanos. Reivindicacion 1: Un compuesto de formula (1) o una sal farmacéuticamente aceptable de dicho compuesto; donde A es - COOalquilo C1-4, ciano, -CHO, -CONH2, -COalquilo C1-4 o Q, donde Q es un anillo de cinco o seis miembros, totalmente saturado, parcialmente insaturado o totalmente insaturado, donde cada átomo del anillo, excepto para el átomo conectado al N de la formula 1, puede reemplazarse por un átomo de nitrogeno, oxigeno o azufre, y donde cada átomo del anillo puede estar opcionalmente sustituido con ciano, una cadena lineal o ramificada, totalmente saturada, parcialmente insaturada o tota mente insaturada, que tiene de 1 a 6 átomos de carbono, o un anillo totalmente saturado, parcialmente insaturado o totalmente insaturado, que tiene de 3 a 8 átomos de carbono, donde cada átomo de carbono de dicha cadena o de dicho anillo se reemplaza opcionalmente por un heteroátomo seleccionado entre nitrogeno, oxigeno y azufre, y dicho átomo de carbono de dicha cadena o de dicho anillo está opcionalmente mono-, di- o trisustituido con amino, halo, ciano, hidroxi, oxo, carboxilo, alcoxicarbonilo C1-6, (alquilo C1-6 opcionalmente sustituido con uno a nueve grupos halo o uno o dos grupos hidroxilo, (alcoxi C1-6 opcionalmente sustituido con uno a nueve grupos halo o uno o dos grupos hidroxilo) o (alquiltio C1-6 opcionalmente sustituido con uno a nueve grupos halo o uno o dos grupos hidroxilo), y dicho átomo de nitrogeno de dicha cadena o de dicho anillo está opcionalmente mono- o disustituido con ciano, oxo, alcoxicarbonilo C1-6 o (alquilo C1-6 opcionalmente sustituido con uno a nueve grupos halo o uno o dos grupos hidroxilo), dicho átomo de azufre de dicha cadena o de dicho anillo está sustituido con uno o dos grupos oxo, uno a cinco grupos fluor o amino, y dicha cadena o dicho anillo está opcionalmente mono- di- o trisustituido con un grupo V, donde V es un anillo de tres a seis miembros, totalmente saturado, parcialmente saturado o totalmente insaturado, que contiene de cero a cuatro heteroátomos seleccionados entre nitrogeno, oxigeno o azufre y opcionalmente sustituido con uno a cinco grupos seleccionados entre hidrogeno, halo, ciano, hidroxi, oxo, carboxilo, alcoxicarbonilo C1-6, (alquilo C1-6 opcionalmente sustituido con uno a nueve grupos halo o uno o dos grupos hidroxilo), (alcoxi C1-6 opcionalmente sustituido con uno a nueve grupos halo o uno o dos grupos hidroxilo) o (alquiltio C1-6 opcionalmente sustituido con uno a nueve grupos halo o uno o dos grupos hidroxilo); B es -NR15R16 o un heterociclo de 3 a 8 miembros que tiene 1 o 2 heteroátomos seleccionados entre oxigeno, nitrogeno y azufre, donde dicho heterociclo está unido a Y en un heteroátomo y donde dicho heterociclo está opcionalmente mono- o di-sustituido con R20, X es C o N, donde si X es N, R4 está ausente; Y es - CR11R12, cada uno de R1, R2, R3, R4, R5, R6 y R7 es independientemente hidrogeno, halo, ciano, hidroxi, nitro, (alquilo C1-6 opcionalmente sustituido con uno a nueve grupos halo, uno o dos grupos hidroxilo, uno o dos alcoxi C1-6, uno o dos grupos amino, uno o dos grupos nitro, ciano, oxo o carboxi), (alcoxi C1-6 opcionalmente sustituido con uno a nueve grupos halo, uno o dos grupos hidroxilo o ciano) o (alquiltio C1-6 opcionalmente sustituido con uno a nueve grupos halo, uno o dos grupos hidroxilo o ciano), o R1 y R2 o R2 y R3 se toman juntos para formar un anillo de 5 a 7 miembros, parcialmente insaturado o totalmente insaturado, donde cada átomo de carbono de dicho anillo se reemplaza opcionalmente por un átomo de oxigeno, donde los átomos de oxigeno no están conectados entre si, donde dicho anillo está opcionalmente mono-, di-, tri- o tetra-sustituido con halo, y opcionalmente mono- o di-sustituido con hidroxi, amino, nitro, ciano, oxo, carboxi, (alquilo C1-6 opcionalmente sustituido con uno a nueve grupos halo, uno o dos grupos hidroxilo, uno o dos grupos alcoxi C1-6, uno o dos grupos amino, uno o dos grupos nitro, ciano, oxo o carboxi) o (alcoxi C1-6 opcionalmente sustituido con uno a nueve grupos halo, uno o dos grupos hidroxilo o ciano); cada R8, R9, R10, R13 y R14 es independientemente hidrogeno, arilo o alquilo C1-6 opcionalmente sustituido con uno a nueve grupos halo; R11 es hidrogeno, arilo, (cicloalquilo C3-6 opcionalmente sustituido con arilo, uno a tres grupos alquilo C1-6, uno a tres grupos alcoxi C1-6, uno a tres grupos haloalquilo C1-6, uno a tres grupos haloalcoxi C1-6, uno o dos grupos hidroxilo o uno a nueve grupos halo) o (alquilo C1-6 donde dicho grupo alquilo C1-6 está opcionalmente sustituido con arilo, uno a tres grupos alcoxi C1-6, uno a tres grupos haloalquilo C1-6, uno a tres grupos haloalcoxi C1-6, uno o dos grupos hidroxilo o uno a nueve grupos halo); R12 es hidrogeno; cada uno de R15 y R16 es independientemente hidrogeno, -alquil C1-6-NR8R9, -alquil C0-6-CO-NR8R9, -alquil C0-6-CO-OR10, -alquil C1-6-NR13-alquil C0-6-CO-O-R10, -alquil C1-6-NR13-alquil C0-6-CO-R14, -alquil C1-6-NR13-alquil C0-6-SO2R10, -alquil C1-6-O-CO-NR8R9, -alquenil C2-6-CO-O-R10, -alquil C0-6-arilo, -alquil C0-6-heteroarilo, -alquil C1-6-O-arilo, -alquil C1-6-O-heteroarilo, -alquil C0-6-heterociclo, -alquil C0-6-cicloalquilo C3-6, -alquil C0-6-cicloalquenilo C3-6, alquinilo C2-6, alquenilo C2-6, alquilo C1-6, ciano o -CO-alquilo C1- 6, donde cada uno de dichos sustituyentes arilo, heteroarilo, heterociclo, cicloalquenilo, cicloalquilo, alquinilo, alquenilo y alquilo está opcionalmente sustituido independientemente con uno a nueve grupos halo, uno o dos grupos hidroxi, uno a tres grupos alquilo C1-6, uno a tres grupos haloalquilo C1-6, uno a tres grupos alcoxi C1-6, uno a tres grupos haloalcoxi C1-6, uno o dos grupos amino, uno o dos grupos nitro, ciano, oxo o carboxi; y cada R20 es independientemente -alquil C0-6- NR8R9, -alquil C0-6-CO-NR8R9, -alquil C0-6-CO-OR10, -alquil C0-6-NR13-alquil C0-6-CO-O-R10, -alquil C0-6-NR13-alquil C0-6-CO-R14, -alquil C0-6-NR13-alquil C0-6-SO2R10, -alquil C0-6-O-CO-NR8R9, -O-alquil C1-6-CO-OR10, halo, -alquenil C2-6-CO-O-R10, - alquil C0-6-arilo, -alquil C0-6-heteroarilo, -alquil C0-6-O-arilo, -alquil C0-6-O-heteroarilo, -alquil C0-6-heterociclo, -alquil C0-6-cicloalquilo C3-6, - alquil C0-6-cicloalquenilo C3-6, alquinilo C2-6, alquenilo C2-6, alquilo C1-6, alcoxi C1-6, oxo, ciano o -CO-alquilo C1-6, donde cada uno de dichos sustituyentes arilo, heteroarilo, heterociclo, cicloalquenilo, cicloalquilo, alquinilo, alquenilo y alquilo está opcionalmente sustituido independientemente con uno a nueve grupos halo, uno o dos grupos hidroxi, uno o dos grupos alquilo C1-6, uno o dos grupos haloalquilo C1-6, uno o dos alcoxi C1-6, uno o dos grupos haloalcoxi C1-6, uno o dos grupos amino, uno o dos grupos nitro, ciano, oxo o carboxi.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US78148806P | 2006-03-10 | 2006-03-10 | |
US11/619,299 US8383660B2 (en) | 2006-03-10 | 2007-01-03 | Dibenzyl amine compounds and derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
AR059802A1 true AR059802A1 (es) | 2008-04-30 |
Family
ID=38085975
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP070100979A AR059802A1 (es) | 2006-03-10 | 2007-03-09 | Compuestos y derivados de dibencilamina, combinaciones y composiciones farmaceuticas que los comprenden y el uso de estos derivados en el tratamiento de enfermedades mediadas por la actividad de cetp. |
Country Status (23)
Country | Link |
---|---|
US (1) | US8383660B2 (es) |
EP (1) | EP1994015B1 (es) |
JP (1) | JP4959731B2 (es) |
KR (1) | KR101059274B1 (es) |
AP (1) | AP2008004603A0 (es) |
AR (1) | AR059802A1 (es) |
AU (1) | AU2007226260B2 (es) |
BR (1) | BRPI0708753A2 (es) |
CA (2) | CA2717242A1 (es) |
CR (1) | CR10265A (es) |
DK (1) | DK1994015T3 (es) |
DO (1) | DOP2007000044A (es) |
ES (1) | ES2410859T3 (es) |
IL (1) | IL193572A (es) |
MA (1) | MA30272B1 (es) |
MX (1) | MX2008011045A (es) |
NL (1) | NL2000527C2 (es) |
NO (1) | NO20083642L (es) |
PE (1) | PE20071022A1 (es) |
RS (1) | RS20080409A (es) |
TW (1) | TW200736235A (es) |
UY (1) | UY30197A1 (es) |
WO (1) | WO2007105049A1 (es) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2008249744A1 (en) * | 2007-05-10 | 2008-11-20 | Pfizer Limited | Azetidine derivatives and their use as prostaglandin E2 antagonists |
SG171914A1 (en) | 2008-12-02 | 2011-07-28 | Chiralgen Ltd | Method for the synthesis of phosphorus atom modified nucleic acids |
AU2010270714B2 (en) | 2009-07-06 | 2015-08-13 | Wave Life Sciences Ltd. | Novel nucleic acid prodrugs and methods use thereof |
CN102241667B (zh) * | 2010-05-14 | 2013-10-23 | 中国人民解放军军事医学科学院毒物药物研究所 | 1-[(4-羟基哌啶-4基)甲基]吡啶-2(1h)-酮衍生物及其制备方法和用途 |
WO2012030165A2 (ko) | 2010-08-31 | 2012-03-08 | 서울대학교산학협력단 | P P A R δ 활성물질의 태자재프로그래밍용도 |
US10428019B2 (en) * | 2010-09-24 | 2019-10-01 | Wave Life Sciences Ltd. | Chiral auxiliaries |
ES2683350T3 (es) | 2011-07-08 | 2018-09-26 | Novartis Ag | Método para tratar la aterosclerosis en sujetos con alto nivel de triglicéridos |
DK2734208T3 (en) | 2011-07-19 | 2017-06-19 | Wave Life Sciences Ltd | PROCEDURES FOR SYNTHESIS OF FUNCTIONALIZED NUCLEIC ACIDS |
SG11201500232UA (en) | 2012-07-13 | 2015-04-29 | Wave Life Sciences Pte Ltd | Chiral control |
JP6246121B2 (ja) | 2012-07-13 | 2017-12-13 | 株式会社新日本科学 | キラル核酸アジュバント |
US9598458B2 (en) | 2012-07-13 | 2017-03-21 | Wave Life Sciences Japan, Inc. | Asymmetric auxiliary group |
CN103351354B (zh) * | 2013-06-09 | 2015-08-12 | 西安近代化学研究所 | 1-甲基-5-氨基四唑合成方法 |
JPWO2015108047A1 (ja) | 2014-01-15 | 2017-03-23 | 株式会社新日本科学 | 免疫誘導活性を有するキラル核酸アジュバンド及び免疫誘導活性剤 |
EP3095460A4 (en) | 2014-01-15 | 2017-08-23 | Shin Nippon Biomedical Laboratories, Ltd. | Chiral nucleic acid adjuvant having anti-allergic activity, and anti-allergic agent |
JPWO2015108048A1 (ja) | 2014-01-15 | 2017-03-23 | 株式会社新日本科学 | 抗腫瘍作用を有するキラル核酸アジュバンド及び抗腫瘍剤 |
US10160969B2 (en) | 2014-01-16 | 2018-12-25 | Wave Life Sciences Ltd. | Chiral design |
US20180244624A1 (en) | 2015-08-17 | 2018-08-30 | Inje University Industry-Academic Cooperation Foundation | Novel isonitramine compound and composition containing same for preventing or treating metabolic diseases |
WO2017030367A1 (ko) * | 2015-08-17 | 2017-02-23 | 인제대학교 산학협력단 | 신규한 이소나이트라민 화합물 및 이를 포함하는 대사성 질환 예방 또는 치료용 조성물 |
Family Cites Families (43)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2161938A (en) | 1934-07-31 | 1939-06-13 | Soc Of Chemical Ind | Imidazolines |
US2970082A (en) | 1958-10-07 | 1961-01-31 | Walker Lab Inc | Aluminum nicotinate compositions for hypercholesteremia |
GB984810A (en) | 1961-10-05 | 1965-03-03 | Farmaceutici Italia | Polypeptides |
US3228943A (en) | 1962-06-11 | 1966-01-11 | Lumilysergol derivatives | |
US3338899A (en) | 1962-07-09 | 1967-08-29 | Aron Samuel | 3-phenyl-5-amino-1, 2, 4-oxadiazole compounds |
US3238215A (en) | 1963-10-17 | 1966-03-01 | Sterling Drug Inc | 1-[(3-, 2-, and 1-indolyl)-lower-alkyl-, lower-alkenyl-, and lower-alkynyl]piperidines |
NL127065C (es) | 1964-04-22 | |||
FR1460571A (fr) | 1965-06-10 | 1966-03-04 | Innothera Lab Sa | Composés thiényl acétiques et leur préparation |
FR6087M (es) | 1967-01-10 | 1968-06-04 | ||
US3511836A (en) | 1967-12-13 | 1970-05-12 | Pfizer & Co C | 2,4,6,7-tetra substituted quinazolines |
NL6903138A (es) | 1968-03-02 | 1969-09-04 | ||
GB1218591A (en) | 1968-04-03 | 1971-01-06 | Delalande Sa | Derivatives of n-(3,4,5-trimethoxy cennamoyl) piperazine and their process of preparation |
CH507249A (de) | 1968-05-31 | 1971-05-15 | Sandoz Ag | Verfahren zur Herstellung von 2-Brom-a-ergokryptin |
FR2092133B1 (es) | 1970-05-06 | 1974-03-22 | Orsymonde | |
GB1435139A (en) | 1972-08-17 | 1976-05-12 | Sumitomo Chemical Co | Thiazole derivatives |
US4146643A (en) | 1973-12-18 | 1979-03-27 | Sandoz Ltd. | Increasing vigilance or treating cerebral insufficiency with substituted vincamines |
NL175059C (nl) | 1974-02-23 | Boehringer Mannheim Gmbh | Bereiding van bloeddrukverlagende stoffen en van preparaten die ze bevatten. | |
DE2733747C2 (de) | 1977-07-27 | 1979-09-27 | Hoechst Ag, 6000 Frankfurt | Verfahren zur Herstellung von 2,2 Dichlorhydrazobenzol |
US4188390A (en) | 1977-11-05 | 1980-02-12 | Pfizer Inc. | Antihypertensive 4-amino-2-[4-(1,4-benzodioxan-2-carbonyl) piperazin-1-yl or homopiperazin-1-yl]quinazolines |
IT1094076B (it) | 1978-04-18 | 1985-07-26 | Acraf | Cicloalchiltriazoli |
JPS56110665A (en) | 1980-02-08 | 1981-09-01 | Yamanouchi Pharmaceut Co Ltd | Sulfamoyl-substituted phenetylamine derivative and its preparation |
US5061798A (en) | 1985-01-18 | 1991-10-29 | Smith Kline & French Laboratories, Ltd. | Benzyl pyridyl and pyridazinyl compounds |
GB8501372D0 (en) | 1985-01-18 | 1985-02-20 | Smith Kline French Lab | Chemical compounds |
GB8531071D0 (en) | 1985-12-17 | 1986-01-29 | Boots Co Plc | Therapeutic compound |
US5284971A (en) | 1992-07-16 | 1994-02-08 | Syntex (U.S.A.) Inc. | 4-(3-cyclohexyl-4-hydroxy or-methoxy phenylsulfonyl) 3,5 dibromo phenyl acetic thyromimetic cholesterol-lowering agents |
ES2108855T3 (es) | 1992-07-21 | 1998-01-01 | Ciba Geigy Ag | Derivados de acido oxamico como agentes hipocolesteremicos. |
DE4435477A1 (de) | 1994-10-04 | 1996-04-11 | Bayer Ag | Cycloalkano-indol- und -azaindol-derivate |
AP779A (en) | 1994-10-27 | 1999-11-03 | Janssen Pharmaceutica Nv | Apolipoprotein-B synthesis inhibitors. |
US5521186A (en) | 1994-10-27 | 1996-05-28 | Janssen Pharmaceutica N.V. | Apolipoprotein-β synthesis inhibitors |
EP0832069B1 (en) | 1995-06-07 | 2003-03-05 | Pfizer Inc. | BIPHENYL-2-CARBOXYLIC ACID-TETRAHYDRO-ISOQUINOLIN-6-YL AMIDE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS INHIBITORS OF MICROSOMAL TRIGLYCERIDE TRANSFER PROTEIN AND/OR APOLIPOPROTEIN B (Apo B) SECRETION |
KR100334567B1 (ko) | 1996-11-27 | 2002-05-03 | 디. 제이. 우드, 스피겔 알렌 제이 | 아포 비-분비/엠티피 억제성 아미드 |
JP2894445B2 (ja) * | 1997-02-12 | 1999-05-24 | 日本たばこ産業株式会社 | Cetp活性阻害剤として有効な化合物 |
EE05452B1 (et) | 2001-06-28 | 2011-08-15 | Pfizer Products Inc. | Triamiidasendatud indoolid, bensofuraanid ja bensotiofeenid kui mikrosomaalse trigltseriidide transportvalgu (MTP) ja/v?i apolipoproteiin B (apoB) sekretsiooni inhibiitorid |
JP2003221376A (ja) | 2001-11-21 | 2003-08-05 | Japan Tobacco Inc | Cetp活性阻害剤 |
US6875780B2 (en) | 2002-04-05 | 2005-04-05 | Warner-Lambert Company | Compounds that modulate PPAR activity and methods for their preparation |
EP1533292B1 (en) | 2002-08-30 | 2007-02-14 | Japan Tobacco Inc. | Dibenzylamine compound and medicinal use thereof |
US6653334B1 (en) * | 2002-12-27 | 2003-11-25 | Kowa Co., Ltd. | Benzoxazole compound and pharmaceutical composition containing the same |
WO2005100298A1 (en) | 2004-04-13 | 2005-10-27 | Merck & Co., Inc. | Cetp inhibitors |
DOP2005000123A (es) | 2004-07-02 | 2011-07-15 | Merck Sharp & Dohme | Inhibidores de cetp |
PE20061124A1 (es) * | 2004-11-23 | 2006-10-13 | Pfizer Prod Inc | Compuestos y derivados de dibencil amina |
CA2605214C (en) * | 2004-12-31 | 2016-07-12 | Reddy Us Therapeutics, Inc. | Benzylamine derivatives as cetp inhibitors |
JP2009513573A (ja) * | 2005-09-30 | 2009-04-02 | メルク エンド カムパニー インコーポレーテッド | コレステリルエステル転送蛋白阻害剤 |
US7919506B2 (en) * | 2006-03-10 | 2011-04-05 | Pfizer Inc. | Dibenzyl amine compounds and derivatives |
-
2007
- 2007-01-03 US US11/619,299 patent/US8383660B2/en not_active Expired - Fee Related
- 2007-02-28 WO PCT/IB2007/000524 patent/WO2007105049A1/en active Application Filing
- 2007-02-28 JP JP2008558923A patent/JP4959731B2/ja not_active Expired - Fee Related
- 2007-02-28 MX MX2008011045A patent/MX2008011045A/es active IP Right Grant
- 2007-02-28 EP EP07705669.5A patent/EP1994015B1/en active Active
- 2007-02-28 AU AU2007226260A patent/AU2007226260B2/en not_active Ceased
- 2007-02-28 CA CA2717242A patent/CA2717242A1/en not_active Abandoned
- 2007-02-28 CA CA2645291A patent/CA2645291C/en not_active Expired - Fee Related
- 2007-02-28 RS RSP-2008/0409A patent/RS20080409A/sr unknown
- 2007-02-28 BR BRPI0708753-5A patent/BRPI0708753A2/pt not_active Application Discontinuation
- 2007-02-28 KR KR1020087022081A patent/KR101059274B1/ko not_active IP Right Cessation
- 2007-02-28 DK DK07705669.5T patent/DK1994015T3/da active
- 2007-02-28 AP AP2008004603A patent/AP2008004603A0/xx unknown
- 2007-02-28 ES ES07705669T patent/ES2410859T3/es active Active
- 2007-03-07 NL NL2000527A patent/NL2000527C2/nl not_active IP Right Cessation
- 2007-03-07 DO DO2007000044A patent/DOP2007000044A/es unknown
- 2007-03-08 UY UY30197A patent/UY30197A1/es not_active Application Discontinuation
- 2007-03-09 PE PE2007000259A patent/PE20071022A1/es not_active Application Discontinuation
- 2007-03-09 AR ARP070100979A patent/AR059802A1/es unknown
- 2007-03-09 TW TW096108178A patent/TW200736235A/zh unknown
-
2008
- 2008-08-20 IL IL193572A patent/IL193572A/en not_active IP Right Cessation
- 2008-08-22 NO NO20083642A patent/NO20083642L/no not_active Application Discontinuation
- 2008-08-29 CR CR10265A patent/CR10265A/es not_active Application Discontinuation
- 2008-09-10 MA MA31226A patent/MA30272B1/fr unknown
Also Published As
Publication number | Publication date |
---|---|
TW200736235A (en) | 2007-10-01 |
JP4959731B2 (ja) | 2012-06-27 |
DK1994015T3 (da) | 2013-06-24 |
NL2000527C2 (nl) | 2008-02-06 |
RS20080409A (en) | 2009-07-15 |
CR10265A (es) | 2008-09-23 |
AU2007226260A1 (en) | 2007-09-20 |
AU2007226260B2 (en) | 2012-02-09 |
KR101059274B1 (ko) | 2011-08-24 |
CA2645291A1 (en) | 2007-09-20 |
UY30197A1 (es) | 2007-10-31 |
MA30272B1 (fr) | 2009-03-02 |
AP2008004603A0 (en) | 2008-10-31 |
IL193572A0 (en) | 2009-05-04 |
MX2008011045A (es) | 2008-09-08 |
NL2000527A1 (nl) | 2007-09-11 |
CA2717242A1 (en) | 2007-09-20 |
PE20071022A1 (es) | 2007-10-06 |
WO2007105049A1 (en) | 2007-09-20 |
CA2645291C (en) | 2011-06-28 |
IL193572A (en) | 2013-02-28 |
BRPI0708753A2 (pt) | 2011-06-28 |
JP2009529573A (ja) | 2009-08-20 |
KR20080093156A (ko) | 2008-10-20 |
DOP2007000044A (es) | 2007-09-15 |
EP1994015B1 (en) | 2013-04-24 |
ES2410859T3 (es) | 2013-07-03 |
US20070213314A1 (en) | 2007-09-13 |
EP1994015A1 (en) | 2008-11-26 |
US8383660B2 (en) | 2013-02-26 |
NO20083642L (no) | 2008-09-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AR059802A1 (es) | Compuestos y derivados de dibencilamina, combinaciones y composiciones farmaceuticas que los comprenden y el uso de estos derivados en el tratamiento de enfermedades mediadas por la actividad de cetp. | |
AR079455A1 (es) | Composiciones para el crecimiento y/o recrecimiento del pelo | |
AR094314A1 (es) | Inhibidores de fosfatidilinositol 3-cinasa | |
ES2649995T3 (es) | Benzamidas | |
AR030523A1 (es) | Compuestos 1,2,3,4-tetrahidroquinolinas 2-sustituidas 4-amino sustituidas, su uso en la preparacion de medicamentos, composiciones farmaceuticas, y equipo que los contiene. | |
CL2014003181A1 (es) | Compuestos derivados de benzamidas n- sustituidas o piridinamidas n-sustituidas; composicion farmaceutica que los comprende; metodo de tratamiento; y su uso para el tratamiento de enfermedades o trastornos seleccionados de dolor, depresion y enfermedades cardiovasculares, respiratorias o psiquiatricas o combinaciones de estas. | |
AR035617A1 (es) | Compuestos derivados de fenetanolamina, combinaciones y formulaciones farmaceuticas de los mismos, proceso para su preparacion, su uso en la preparacion de medicamentos para el tratamiento o profilaxis de una condicion clinica para la cual se indica un agonista beta2 adreno-receptor e intermediarios | |
AR053162A1 (es) | Compuesto 5 - oxo - pirrolidin sustituido, composicion farmaceutica que lo comprende y su uso para preparar un medicamento para el tratamiento del glaucoma. | |
AR094277A1 (es) | Derivados de fumarato sustituidos con deuterio | |
PE20090060A1 (es) | ANALOGOS DE IMIDAZOLOPIRIMIDINA Y SU USO COMO INHIBIDORES DE PI3 CINASA Y mTOR | |
PE20151890A1 (es) | Analogos de piridazina 1,4-disustituida y metodos para el tratamiento de condiciones relacionadas con la deficiencia de smn | |
AR056873A1 (es) | Derivados de pirazolopirimidinas como inhibidores de quinasa dependientes de ciclina, composiciones farmaceuticas | |
AR079226A1 (es) | Espiroindolinona- pirrolidinas, procesos de preparacion y uso de los mismos para el tratamiento y profilaxis del cancer | |
AR046297A1 (es) | Inhibidores de la dpp - iv metodos para prepararlos y composiciones farmaceuticas que los contienen como agente activo | |
AR078507A1 (es) | Compuestos lipidicos, composiciones farmaceuticas, usos y metodo de preparacion | |
AR094647A1 (es) | Análogos de 7,8-morfinano cíclico | |
AR091156A1 (es) | Nucleosidos de espirooxetano de uracilo | |
EA201590450A1 (ru) | Сульфамоил-ариламиды и их применение в качестве лекарственных препаратов для лечения гепатита b | |
AR063706A1 (es) | Determinadas amidas sustituidas, el uso de las mismas para el tratamiento de enfermedades mediadas por la inhibicion de la actividad de btk y composiciones farmaceuticas que las comprenden. | |
AR063602A1 (es) | Derivados de espiroindolinona, formulaciones farmaceuticas que los contienen y su uso en la obtencion de un medicamento para el tratamiento de trastornos oncologicos. | |
RU2012140961A (ru) | ПРОИЗВОДНОЕ 1,3,4,8-ТЕТРАГИДРО-2Н-ПИРИДО[1,2-a]ПИРАЗИНА И ЕГО ПРИМЕНЕНИЕ В КАЧЕСТВЕ ИНИБИТОРА ИНТЕГРАЗЫ ВИЧ | |
AR068639A1 (es) | Derivados de biarilo | |
ES2587953T3 (es) | Amidas cíclicas como inhibidores de MetAP-2 | |
AR055041A1 (es) | Tiadiazoles y oxadiazoles como inhibidores de la sintesis de leucotrienos. composiciones farmaceuticas. | |
AR085549A1 (es) | DERIVADOS TRIAZOLIL PIPERAZINA Y TRIAZOLIL PIPERIDINA SUSTITUIDOS COMO MODULADORES DE g SECRETASA |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FB | Suspension of granting procedure |