MA31754B1 - Cis-imidazolines chirales - Google Patents
Cis-imidazolines chiralesInfo
- Publication number
- MA31754B1 MA31754B1 MA32739A MA32739A MA31754B1 MA 31754 B1 MA31754 B1 MA 31754B1 MA 32739 A MA32739 A MA 32739A MA 32739 A MA32739 A MA 32739A MA 31754 B1 MA31754 B1 MA 31754B1
- Authority
- MA
- Morocco
- Prior art keywords
- chirales
- imidazolines
- cis
- compounds
- agents
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 abstract 3
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 239000002246 antineoplastic agent Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
-
- 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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D403/14—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 three or more hetero rings
-
- 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
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur 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
- C07D417/14—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 three or more hetero rings
-
- 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
- C07D471/10—Spiro-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
L'INVENTION PORTE SUR DES COMPOSÉS REPRÉSENTÉS PAR LA FORMULE (I), OU SUR LEURS SELS PHARMACEUTIQUEMENT ACCEPTABLES, FORMULE DANS LAQUELLE X, Y, Z, V1, V2, R1, R2, R3, R4 ET R5 SONT TELS QUE PRÉSENTEMENT DÉCRITS, SUR DES PROCÉDÉS D'OBTENTION DESDITS COMPOSÉS, ET SUR DES PRÉPARATIONS PHARMACEUTIQUES LES CONTENANT. CES COMPOSÉS SONT UTILES COMME AGENTS ANTI-CANCER, EN PARTICULIER COMME AGENTS DANS LE TRAITEMENT DE TUMEURS SOLIDES.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US97850607P | 2007-10-09 | 2007-10-09 | |
| US9275908P | 2008-08-29 | 2008-08-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA31754B1 true MA31754B1 (fr) | 2010-10-01 |
Family
ID=40149549
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA32739A MA31754B1 (fr) | 2007-10-09 | 2010-04-05 | Cis-imidazolines chirales |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US8513239B2 (fr) |
| EP (2) | EP2203437B1 (fr) |
| JP (1) | JP5324586B2 (fr) |
| KR (1) | KR101203020B1 (fr) |
| CN (2) | CN101821251A (fr) |
| AR (1) | AR068742A1 (fr) |
| AU (1) | AU2008309759A1 (fr) |
| BR (1) | BRPI0817850A2 (fr) |
| CA (1) | CA2701932C (fr) |
| CL (1) | CL2008002982A1 (fr) |
| CO (1) | CO6280486A2 (fr) |
| CR (1) | CR11333A (fr) |
| ES (1) | ES2395210T3 (fr) |
| IL (1) | IL204653A0 (fr) |
| MA (1) | MA31754B1 (fr) |
| MX (1) | MX2010003868A (fr) |
| PE (1) | PE20090814A1 (fr) |
| RU (1) | RU2487127C2 (fr) |
| TW (1) | TW200916446A (fr) |
| WO (1) | WO2009047161A1 (fr) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2375899B1 (fr) * | 2009-01-12 | 2015-02-25 | Array Biopharma Inc. | Composés contenant de la pipéridine et leur utilisation dans le traitement du diabète |
| WO2010132873A2 (fr) | 2009-05-15 | 2010-11-18 | Northwestern University | Composés à noyau pyrrolidine chiraux utilisés pour la préparation d'inhibiteurs d'oxyde nitrique synthase |
| WO2011073154A1 (fr) | 2009-12-17 | 2011-06-23 | Boehringer Ingelheim International Gmbh | Nouveaux antagonistes du récepteur ccr2 et leurs utilisations |
| WO2011073155A1 (fr) | 2009-12-17 | 2011-06-23 | Boehringer Ingelheim International Gmbh | Nouveaux antagonistes du récepteur ccr2 et leurs utilisations |
| US8877745B2 (en) | 2010-05-12 | 2014-11-04 | Boehringer Ingelheim International Gmbh | CCR2 receptor antagonists, method for producing the same, and use thereof as medicaments |
| US9018212B2 (en) | 2010-05-25 | 2015-04-28 | Boehringer Ingelheim International Gmbh | Pyridazine carboxamides as CCR2 receptor antagonists |
| EP2576538B1 (fr) | 2010-06-01 | 2015-10-28 | Boehringer Ingelheim International GmbH | Nouveaux antagonistes de CCR2 |
| JO2998B1 (ar) | 2010-06-04 | 2016-09-05 | Amgen Inc | مشتقات بيبيريدينون كمثبطات mdm2 لعلاج السرطان |
| US9266860B2 (en) | 2010-09-30 | 2016-02-23 | St. Jude Children's Research Hospital | Aryl-substituted imidazoles |
| JP2014507384A (ja) * | 2010-12-16 | 2014-03-27 | ロシュ グリクアート アーゲー | Mdm2阻害剤とのアフコシル化cd20抗体の併用療法 |
| AU2012316055B2 (en) | 2011-09-27 | 2016-05-12 | Amgen Inc. | Heterocyclic compounds as MDM2 inhibitors for the treatment of cancer |
| WO2014082889A1 (fr) * | 2012-11-28 | 2014-06-05 | F. Hoffmann-La Roche Ag | Nouvelles imidazolines utilisées en tant que doubles inhibiteurs de mdm2 et mdmx |
| EP2935263B1 (fr) | 2012-12-20 | 2018-12-05 | Merck Sharp & Dohme Corp. | Imidazopyridines substituées en tant qu'inhibiteurs d'hdm2 |
| US11407721B2 (en) | 2013-02-19 | 2022-08-09 | Amgen Inc. | CIS-morpholinone and other compounds as MDM2 inhibitors for the treatment of cancer |
| CA2902856C (fr) | 2013-02-28 | 2021-02-16 | Amgen Inc. | Inhibiteur mdm2 derive de l'acide benzoique pour le traitement du cancer |
| HRP20191860T1 (hr) | 2013-03-13 | 2019-12-27 | Forma Therapeutics, Inc. | Derivati 2-hidroksi-1-{4-[(4-fenilfenil)karbonil]piperazin-1-il}etan-1-ona i srodni spojevi kao inhibitori sintaze masnih kiselina (fasn) za liječenje raka |
| WO2014151863A1 (fr) | 2013-03-14 | 2014-09-25 | Amgen Inc. | Composés morpholinone d'acide hétéroaryle utilisés comme inhibiteurs de mdm2 pour le traitement du cancer |
| MA53572A1 (fr) | 2013-06-10 | 2021-10-29 | Amgen Inc | Procédés de production et formes cristallines d'un inhibiteur mdm2 |
| US10758525B2 (en) | 2015-01-22 | 2020-09-01 | MyoKardia, Inc. | 4-methylsulfonyl-substituted piperidine urea compounds |
| CN118436801A (zh) | 2016-05-20 | 2024-08-06 | 豪夫迈·罗氏有限公司 | Protac抗体缀合物及其使用方法 |
| CN105906610B (zh) * | 2016-05-24 | 2018-10-23 | 绍兴文理学院 | 一种3-(4-苯基-1h-咪唑-5-基)-1h-吲哚衍生物及其制备方法和应用 |
| EP3415802B1 (fr) | 2017-06-14 | 2019-08-28 | Borealis AG | Raccord de dilatation |
| CN117186108B (zh) * | 2018-03-26 | 2025-08-19 | 诺华股份有限公司 | 布鲁顿酪氨酸激酶降解剂 |
| WO2020092395A1 (fr) | 2018-10-29 | 2020-05-07 | Forma Therapeutics, Inc. | Formes solides de (4-(2-fluoro-4-(1-méthyl-1h-benzo[d]imidazol-5-yl)benzoyl)pipérazin-1-yl)(1-hydroxycyclopropyl)méthanone |
| AU2020315605A1 (en) | 2019-07-16 | 2022-03-03 | MyoKardia, Inc. | Polymorphic forms of (R)-4-(1-((3-(difluoromethyl)-1-methyl-1H-pyrazol-4-yl)sulfonyl)-1-fluoroethyl)-N-(isoxazol-3-yl)piperidine-1-carboxamide |
| EP4146645B1 (fr) * | 2020-05-07 | 2025-06-25 | ONO Pharmaceutical Co., Ltd. | Dérivés de 3-azabicyclo(3.1.0)hexane ayant une activité inhibitrice de kdm5 et leur utilisation |
| WO2023056069A1 (fr) | 2021-09-30 | 2023-04-06 | Angiex, Inc. | Conjugués agent de dégradation-anticorps et leurs procédés d'utilisation |
| JP7743829B2 (ja) * | 2021-11-05 | 2025-09-25 | 小野薬品工業株式会社 | Kdm5阻害作用を有する化合物を含有する医薬組成物 |
| WO2024240858A1 (fr) | 2023-05-23 | 2024-11-28 | Valerio Therapeutics | Molécules protac dirigées contre un système de réparation de dommages à l'adn et leurs utilisations |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02101065A (ja) | 1988-10-06 | 1990-04-12 | Tanabe Seiyaku Co Ltd | イミダゾリン誘導体及びその製法 |
| GB2351082A (en) | 1999-06-18 | 2000-12-20 | Lilly Forschung Gmbh | Synthesis of Cyclic Substituted Amidines |
| CN100486969C (zh) | 2001-12-18 | 2009-05-13 | 霍夫曼-拉罗奇有限公司 | 顺式-2,4,5-三苯基-咪唑啉及其在肿瘤治疗中的应用 |
| PL370909A1 (en) * | 2001-12-18 | 2005-05-30 | F.Hoffmann-La Roche Ag | Cis-imidazolines as mdm2 inhibitors |
| EP1753727B1 (fr) | 2004-05-18 | 2008-11-19 | F.Hoffmann-La Roche Ag | Nouvelles cis-imidazolines |
| WO2007006301A1 (fr) | 2005-07-08 | 2007-01-18 | Vestas Wind Systems A/S | Eolienne, moyeu d'eolienne et utilisation |
| KR20100129331A (ko) * | 2005-12-01 | 2010-12-08 | 에프. 호프만-라 로슈 아게 | 항암제로서 사용하기 위한 p53 및 mdm2 단백질 간 상호작용의 저해제로서의 2,4,5-트리페닐 이미다졸린 유도체 |
| WO2007082805A1 (fr) * | 2006-01-18 | 2007-07-26 | F. Hoffmann-La Roche Ag | Imidazolines cis-4,5-biaryl-2-hétérocycliques utilisées comme inhibiteurs de mdm2 |
-
2008
- 2008-09-30 CA CA2701932A patent/CA2701932C/fr not_active Expired - Fee Related
- 2008-09-30 CN CN200880110704A patent/CN101821251A/zh active Pending
- 2008-09-30 KR KR1020107007374A patent/KR101203020B1/ko not_active Expired - Fee Related
- 2008-09-30 ES ES08837881T patent/ES2395210T3/es active Active
- 2008-09-30 JP JP2010528361A patent/JP5324586B2/ja not_active Expired - Fee Related
- 2008-09-30 CN CN201510024021.1A patent/CN104710408A/zh active Pending
- 2008-09-30 RU RU2010118018/04A patent/RU2487127C2/ru active
- 2008-09-30 AU AU2008309759A patent/AU2008309759A1/en not_active Abandoned
- 2008-09-30 MX MX2010003868A patent/MX2010003868A/es active IP Right Grant
- 2008-09-30 EP EP08837881A patent/EP2203437B1/fr active Active
- 2008-09-30 WO PCT/EP2008/063053 patent/WO2009047161A1/fr not_active Ceased
- 2008-09-30 BR BRPI0817850 patent/BRPI0817850A2/pt not_active Application Discontinuation
- 2008-09-30 EP EP10175975A patent/EP2325180A1/fr not_active Withdrawn
- 2008-10-07 PE PE2008001740A patent/PE20090814A1/es not_active Application Discontinuation
- 2008-10-07 AR ARP080104381A patent/AR068742A1/es not_active Application Discontinuation
- 2008-10-07 CL CL2008002982A patent/CL2008002982A1/es unknown
- 2008-10-08 TW TW097138773A patent/TW200916446A/zh unknown
- 2008-10-09 US US12/248,095 patent/US8513239B2/en not_active Expired - Fee Related
-
2010
- 2010-03-22 IL IL204653A patent/IL204653A0/en unknown
- 2010-03-24 CR CR11333A patent/CR11333A/es not_active Application Discontinuation
- 2010-03-26 CO CO10036293A patent/CO6280486A2/es not_active Application Discontinuation
- 2010-04-05 MA MA32739A patent/MA31754B1/fr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US20090111789A1 (en) | 2009-04-30 |
| EP2325180A1 (fr) | 2011-05-25 |
| MX2010003868A (es) | 2010-04-27 |
| CO6280486A2 (es) | 2011-05-20 |
| CL2008002982A1 (es) | 2009-10-16 |
| KR20100051742A (ko) | 2010-05-17 |
| CN104710408A (zh) | 2015-06-17 |
| RU2487127C2 (ru) | 2013-07-10 |
| WO2009047161A1 (fr) | 2009-04-16 |
| EP2203437B1 (fr) | 2012-11-07 |
| CR11333A (es) | 2010-06-21 |
| PE20090814A1 (es) | 2009-06-27 |
| CN101821251A (zh) | 2010-09-01 |
| KR101203020B1 (ko) | 2012-11-20 |
| AR068742A1 (es) | 2009-12-02 |
| ES2395210T3 (es) | 2013-02-11 |
| JP5324586B2 (ja) | 2013-10-23 |
| IL204653A0 (en) | 2010-11-30 |
| CA2701932A1 (fr) | 2009-04-16 |
| AU2008309759A1 (en) | 2009-04-16 |
| JP2010540675A (ja) | 2010-12-24 |
| US8513239B2 (en) | 2013-08-20 |
| EP2203437A1 (fr) | 2010-07-07 |
| TW200916446A (en) | 2009-04-16 |
| BRPI0817850A2 (pt) | 2015-04-07 |
| CA2701932C (fr) | 2015-10-20 |
| RU2010118018A (ru) | 2011-11-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA54653B1 (fr) | Modulateurs du récepteur de cxcr7 pipéridine | |
| MA28747B1 (fr) | Dérivés de pyridine | |
| MA32711B1 (fr) | Pyrrolidine-2-carboxamides substitues | |
| MA29926B1 (fr) | Derives de pyrazine | |
| TN2009000450A1 (fr) | Derives de pyridine | |
| MA32965B1 (fr) | Derives de sulfonamides | |
| TNSN08445A1 (fr) | Derives de triazolopyrazine utiles comme agent anticancereux | |
| MA27568A1 (fr) | Derives de pyrrolopyrimidine | |
| MA31142B1 (fr) | Derives heteroaryles de pyrrolidinyl et piperdinyl cetones. | |
| TN2010000175A1 (fr) | Piperidino-dihydrothienopyrimidines substituees | |
| MA28270A1 (fr) | Pyrido [2, 3-D] pyrimidine-2, 4-diamines servant d'inhibiteurs de PDE 2 | |
| MA30352B1 (fr) | Pyridine [3,4-b] pyrazinones | |
| MA27774A1 (fr) | Inhibiteurs de phosphatidylinositol 3-kinase | |
| MA56883B1 (fr) | Dérivés de 2-hydroxycycloalcane-1-carbamoyle | |
| MA31766B1 (fr) | Composés organiques | |
| MA31894B1 (fr) | Composes organiques | |
| MA31683B1 (fr) | Composes et procedes pour moduler fxr | |
| MA30291B1 (fr) | Derives de l'azolopyridin-3-one en tant qu'inhibiteurs de la lipase endotheliale | |
| MA29856B1 (fr) | Derives de diacylindazole en tant qu'inhibiteurs de lipases et de phospholipases | |
| MA28007A1 (fr) | Composes organiques | |
| MA43639B1 (fr) | Nouveaux dérivés d'ammonium, procédé de préparation de ceux-ci et compositions pharmaceutiques les contenant | |
| TN2009000471A1 (fr) | Composes amino-heterocycliques | |
| MA31952B1 (fr) | Pyrrolopyrimidines et pyrrolopyridines | |
| MA40225B1 (fr) | Composés dihydroisoquinolinone substitués | |
| MA31873B1 (fr) | Inhibiteurs de la peptide déformylase |