MA33976B1 - Spiroindolinone pyrrolidines - Google Patents
Spiroindolinone pyrrolidinesInfo
- Publication number
- MA33976B1 MA33976B1 MA34939A MA34939A MA33976B1 MA 33976 B1 MA33976 B1 MA 33976B1 MA 34939 A MA34939 A MA 34939A MA 34939 A MA34939 A MA 34939A MA 33976 B1 MA33976 B1 MA 33976B1
- Authority
- MA
- Morocco
- Prior art keywords
- spiroindolinone
- pyrrolidines
- compounds
- spiroindolinone pyrrolidines
- simulations
- Prior art date
Links
- 150000003235 pyrrolidines Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 238000004088 simulation Methods 0.000 abstract 1
Classifications
-
- 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
- C07D487/10—Spiro-condensed systems
-
- 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
- A61K31/407—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 condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
L'invention concerne des composés de la formule (i) dans laquelle x, y et r1 à r8 sont décrits par les présentes ainsi que les énantiomères, les sels de qualité pharmaceutique et les esters de ceux-ci. Les composés sont utiles comme agents anticancéreux.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US26579209P | 2009-12-02 | 2009-12-02 | |
| US38805410P | 2010-09-30 | 2010-09-30 | |
| PCT/EP2010/068353 WO2011067185A1 (fr) | 2009-12-02 | 2010-11-29 | Spiroindolinone pyrrolidines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA33976B1 true MA33976B1 (fr) | 2013-02-01 |
Family
ID=43608656
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA34939A MA33976B1 (fr) | 2009-12-02 | 2010-11-29 | Spiroindolinone pyrrolidines |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US8088815B2 (fr) |
| EP (1) | EP2507243B1 (fr) |
| JP (1) | JP5647262B2 (fr) |
| KR (1) | KR101418191B1 (fr) |
| CN (1) | CN102741257B (fr) |
| AR (1) | AR079226A1 (fr) |
| AU (1) | AU2010326855B2 (fr) |
| BR (1) | BR112012012872A2 (fr) |
| CA (1) | CA2781823A1 (fr) |
| CL (1) | CL2012001405A1 (fr) |
| CO (1) | CO6541606A2 (fr) |
| CR (1) | CR20120259A (fr) |
| EC (1) | ECSP12011945A (fr) |
| ES (1) | ES2543468T3 (fr) |
| IL (1) | IL220010A (fr) |
| MA (1) | MA33976B1 (fr) |
| MX (1) | MX2012006260A (fr) |
| MY (1) | MY160596A (fr) |
| NZ (1) | NZ600024A (fr) |
| PE (1) | PE20121334A1 (fr) |
| PH (1) | PH12012501029A1 (fr) |
| RU (1) | RU2571100C2 (fr) |
| SG (1) | SG181465A1 (fr) |
| TW (1) | TW201129571A (fr) |
| WO (1) | WO2011067185A1 (fr) |
| ZA (1) | ZA201204036B (fr) |
Families Citing this family (55)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL2118123T3 (pl) | 2007-01-31 | 2016-06-30 | Dana Farber Cancer Inst Inc | Stabilizowane peptydy p53 i ich zastosowania |
| KR101525754B1 (ko) | 2007-03-28 | 2015-06-09 | 프레지던트 앤드 펠로우즈 오브 하바드 칼리지 | 스티칭된 폴리펩티드 |
| JP2013510860A (ja) | 2009-11-12 | 2013-03-28 | ザ、リージェンツ、オブ、ザ、ユニバーシティ、オブ、ミシガン | スピロ−オキシインドールmdm2アンタゴニスト |
| US20110118283A1 (en) * | 2009-11-17 | 2011-05-19 | Qingjie Ding | Substituted Pyrrolidine-2-Carboxamides |
| US8288431B2 (en) * | 2010-02-17 | 2012-10-16 | Hoffmann-La Roche Inc. | Substituted spiroindolinones |
| JO2998B1 (ar) | 2010-06-04 | 2016-09-05 | Amgen Inc | مشتقات بيبيريدينون كمثبطات mdm2 لعلاج السرطان |
| CA2807685C (fr) | 2010-08-13 | 2020-10-06 | Aileron Therapeutics, Inc. | Macrocycle peptidomimetique derive de p53 |
| US20120046306A1 (en) * | 2010-08-18 | 2012-02-23 | David Joseph Bartkovitz | Substituted Heteroaryl Spiropyrrolidine MDM2 Antagonists |
| TWI535723B (zh) | 2010-11-12 | 2016-06-01 | 密西根大學董事會 | 螺-吲哚酮mdm2拮抗劑 |
| RU2612534C2 (ru) | 2011-03-10 | 2017-03-09 | Дайити Санкио Компани, Лимитед | Диспиропирролидиновые производные |
| SG194873A1 (en) | 2011-05-11 | 2013-12-30 | Sanofi Sa | Spiro-oxindole mdm2 antagonists |
| WO2013049250A1 (fr) | 2011-09-27 | 2013-04-04 | Amgen Inc. | Heterocycles utilises comme inhibiteurs de mdm2 dans le traitement du cancer |
| TW201806968A (zh) | 2011-10-18 | 2018-03-01 | 艾利倫治療公司 | 擬肽巨環化合物 |
| CA2864120A1 (fr) | 2012-02-15 | 2013-08-22 | Aileron Therapeutics, Inc. | Macrocycles peptidomimetiques reticules par triazole et par thioether |
| BR112014020103A2 (pt) | 2012-02-15 | 2018-10-09 | Aileron Therapeutics, Inc. | macrociclos peptidomiméticos |
| TWI586668B (zh) | 2012-09-06 | 2017-06-11 | 第一三共股份有限公司 | 二螺吡咯啶衍生物之結晶 |
| KR20150082307A (ko) | 2012-11-01 | 2015-07-15 | 에일러론 테라퓨틱스 인코포레이티드 | 이치환 아미노산 및 이의 제조 및 사용 방법 |
| BR112015013611A2 (pt) | 2012-12-20 | 2017-11-14 | Merck Sharp & Dohme | composto, e, composição farmacêutica |
| CN103113854B (zh) * | 2013-02-06 | 2015-11-18 | 青岛奥环新能源科技发展有限公司 | 一种移动供热用复合相变材料及其制备方法 |
| US11407721B2 (en) | 2013-02-19 | 2022-08-09 | Amgen Inc. | CIS-morpholinone and other compounds as MDM2 inhibitors for the treatment of cancer |
| AU2014223547B2 (en) * | 2013-02-28 | 2017-11-16 | Amgen Inc. | A benzoic acid derivative MDM2 inhibitor for the treatment of cancer |
| EP2970237B1 (fr) | 2013-03-14 | 2017-09-27 | Amgen Inc. | Composés morpholinone d'acide hétéroaryle utilisés comme inhibiteurs de mdm2 pour le traitement du cancer |
| JOP20200296A1 (ar) | 2013-06-10 | 2017-06-16 | Amgen Inc | عمليات صنع وأشكال بلورية من mdm2 مثبط |
| CN103342672B (zh) * | 2013-07-02 | 2015-12-23 | 扬州大学 | 取代吡咯烷-2-酮的新合成方法 |
| CA2945527C (fr) | 2014-04-17 | 2022-05-17 | The Regents Of The University Of Michigan | Inhibiteurs de hdac et methodes therapeutiques les utilisant |
| US10576064B2 (en) | 2014-07-03 | 2020-03-03 | Boehringer Ingelheim International Gmbh | Spiro[3H-indole-3,2′-pyrrolidin]-2(1H)-one compounds and derivatives as MDM2-P53 inhibitors |
| WO2016028391A2 (fr) * | 2014-08-18 | 2016-02-25 | Hudson Biopharma Inc. | Spiropyrrolidines utiles en tant qu'inhibiteurs de mdm2 |
| HRP20191414T1 (hr) | 2014-08-21 | 2019-11-01 | Boehringer Ingelheim Int | Novi spojevi i derivati spiro[3h-indol-3,2'-pirolidin]-2(1h)-ona kao mdm1-p53-inhibitori |
| MX2017003797A (es) | 2014-09-24 | 2017-06-15 | Aileron Therapeutics Inc | Macrociclos peptidomimeticos y usos de los mismos. |
| SG10201902598VA (en) | 2014-09-24 | 2019-04-29 | Aileron Therapeutics Inc | Peptidomimetic macrocycles and formulations thereof |
| US10253067B2 (en) | 2015-03-20 | 2019-04-09 | Aileron Therapeutics, Inc. | Peptidomimetic macrocycles and uses thereof |
| RU2629750C2 (ru) * | 2015-04-09 | 2017-09-01 | Ян Андреевич Иваненков | НОВЫЕ ДИСПИРО-ИНДОЛИНОНЫ, ИНГИБИТОРЫ MDM2/p53 ВЗАИМОДЕЙСТВИЯ, СПОСОБ ПОЛУЧЕНИЯ И ПРИМЕНЕНИЯ |
| CN108368161A (zh) | 2015-09-10 | 2018-08-03 | 艾瑞朗医疗公司 | 作为mcl-1调节剂的拟肽大环化合物 |
| HUE054985T2 (hu) | 2015-10-09 | 2021-11-29 | Boehringer Ingelheim Int | Spiro[3H-indol-3,2'-pirrolidin]-2(1H)-on vegyületek és számrazékok, mint MDM2-P53 inhibitorok |
| GB201603779D0 (en) * | 2016-03-04 | 2016-04-20 | Mission Therapeutics Ltd | Novel compounds |
| CN113788818A (zh) * | 2016-04-06 | 2021-12-14 | 密执安大学评议会 | Mdm2蛋白质降解剂 |
| CN105949221B (zh) * | 2016-05-11 | 2017-08-25 | 湖南科技大学 | 一种含螺吲哚‑2‑酮衍生物及其制备方法和作为抗癌药物的应用 |
| CN109152843A (zh) | 2016-05-20 | 2019-01-04 | 豪夫迈·罗氏有限公司 | Protac抗体缀合物及其使用方法 |
| JP6848047B2 (ja) * | 2016-08-08 | 2021-03-24 | フェイ シアオ, | スピロインドロンポリエチレングリコールカーボネート系化合物及びその組成物、調製方法及びその使用 |
| EP3511334A1 (fr) * | 2018-01-16 | 2019-07-17 | Adamed sp. z o.o. | Composés de 1,2,3',5'-tetrahydro-2'h-spiro[indole-3,1'-pyrrolo[3,4-c]pyrrole] -2,3'-dione comme agents thérapeutiques activant le tp53 |
| RU2730287C1 (ru) * | 2019-08-30 | 2020-08-21 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Московский государственный университет имени М.В. Ломоносова" (МГУ) | Новые 2',5'-диарилспиро[индол-3,3'-пирролидин]-2(1н)-оны и способ их получения |
| GB201919219D0 (en) | 2019-12-23 | 2020-02-05 | Otsuka Pharma Co Ltd | Cancer biomarkers |
| US20230313313A1 (en) | 2020-08-27 | 2023-10-05 | Otsuka Pharmaceutical Co., Ltd. | Biomarkers for cancer therapy using mdm2 antagonists |
| US20250073340A1 (en) * | 2021-01-23 | 2025-03-06 | Newave Pharmaceutical Inc. | Spirocyclic mdm2 modulator and uses thereof |
| GB202103080D0 (en) | 2021-03-04 | 2021-04-21 | Otsuka Pharma Co Ltd | Cancer biomarkers |
| CN115215872A (zh) * | 2021-04-15 | 2022-10-21 | 中国科学院上海药物研究所 | 具有取代苯基螺[吲哚啉-3,3′-吡咯烷]结构的小分子化合物 |
| US12398147B2 (en) | 2021-05-11 | 2025-08-26 | Enanta Pharmaceuticals, Inc. | Macrocyclic spiropyrrolidine derived antiviral agents |
| CN113387957B (zh) * | 2021-06-09 | 2022-08-09 | 江苏亚尧生物科技有限公司 | 螺环吲哚酮-吡咯烷碳酸酯化合物和其组合物、制备方法及用途 |
| US12479854B2 (en) | 2021-07-29 | 2025-11-25 | Enanta Pharmaceuticals, Inc. | Spiropyrrolidine derived antiviral agents |
| WO2023056069A1 (fr) | 2021-09-30 | 2023-04-06 | Angiex, Inc. | Conjugués agent de dégradation-anticorps et leurs procédés d'utilisation |
| WO2023086400A1 (fr) * | 2021-11-12 | 2023-05-19 | Enanta Pharmaceuticals, Inc. | Nouveaux agents antiviraux dérivés de spiropyrrolidine |
| WO2023107419A1 (fr) | 2021-12-08 | 2023-06-15 | Enanta Pharmaceuticals, Inc. | Composés spirocycliques saturés utilisés comme agents antiviraux |
| CN116283701B (zh) * | 2021-12-21 | 2025-04-22 | 中国科学院上海药物研究所 | 具有4-(取代氨甲基)-5-新戊基-n-取代基吡咯烷-2-甲酰胺结构的化合物 |
| CN114773327B (zh) * | 2022-04-18 | 2023-08-18 | 广东优康精细化工有限公司 | 一种吡噻菌胺中间体的制备方法 |
| 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 |
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| US2759935A (en) | 1953-02-18 | 1956-08-21 | Bristol Lab Inc | Substituted 3-phenyloxindoles |
| US3441570A (en) | 1966-01-20 | 1969-04-29 | Parke Davis & Co | 3-tertiary aminoalkylamino-3-phenyl oxindole compounds |
| US3686210A (en) | 1970-01-13 | 1972-08-22 | American Home Prod | 2-acylamido-3-aryl-3h-indol-3-ol esters and related compounds |
| US4020179A (en) | 1975-05-15 | 1977-04-26 | Richardson-Merrell Inc. | 7-Substituted-2-indolinones |
| JPS55129284A (en) | 1979-03-27 | 1980-10-06 | Shionogi & Co Ltd | 3-(1-imipazolyl)indolin-2-one |
| DE3714473A1 (de) | 1987-04-30 | 1988-11-10 | Basf Ag | Kontinuierliches verfahren zur epimerisierung von zuckern, insbesondere von d-arabinose zu d-ribose |
| RU2084449C1 (ru) * | 1994-03-02 | 1997-07-20 | Всероссийский научный центр по безопасности биологически активных веществ | 1-бензил-2-оксотриптамин гидрохлорид и его производные, обладающие гепатозащитной активностью |
| FR2740136B1 (fr) | 1995-10-24 | 1998-01-09 | Sanofi Sa | Derives d'indolin-2-one, procede pour leur preparation et les compositions pharmaceutiques les contenant |
| AU7450898A (en) | 1997-05-28 | 1998-12-30 | Tokyo Tanabe Company Limited | Indole compounds |
| US6511974B1 (en) | 1997-07-30 | 2003-01-28 | Wyeth | Tricyclic vasopressin agonists |
| EP0947511A1 (fr) | 1998-03-30 | 1999-10-06 | F. Hoffmann-La Roche Ag | Dérivés de l'acide phénoxyacétique et de phénoxyméthyltétrazole ayant une activité antitumorale |
| GB9819860D0 (en) | 1998-09-12 | 1998-11-04 | Zeneca Ltd | Chemical compounds |
| JP2000191661A (ja) | 1998-12-25 | 2000-07-11 | Mitsubishi-Tokyo Pharmaceuticals Inc | 環状アミド化合物 |
| CA2373990C (fr) | 1999-05-21 | 2007-05-08 | Bristol-Myers Squibb Company | Pyrrolotriazines inhibiteurs de kinases |
| BR0012590A (pt) | 1999-07-21 | 2002-04-09 | Astrazeneca Ab | Composto, processo para a preparação do mesmo, formulação farmacêutica, uso de um composto, e, métodos para tratamento ou profilaxia de dor ou desconforto, e para tratamento ou profilaxia de dor neuropática ou central |
| FR2827604B1 (fr) | 2001-07-17 | 2003-09-19 | Sanofi Synthelabo | Nouveaux derives de 1-phenylsulfonyl-1,3-dihydro-2h-indol-2- one, un procede pour leur preparation et les compositions pharmaceutiques en contenant |
| WO2003078394A1 (fr) | 2002-03-15 | 2003-09-25 | Eli Lilly And Company | Derives de dihydroindol-2-one modulant le recepteur nucleaire de l'hormone steroide |
| DE202004014849U1 (de) * | 2004-09-23 | 2005-02-03 | Trw Automotive Safety Systems Gmbh | Vorrichtung zur Bestimmung eines absoluten Drehwinkels |
| WO2006080574A1 (fr) | 2005-01-28 | 2006-08-03 | Taisho Pharmaceutical Co., Ltd. | Compose 1,3-dihydro-2h-indole-2-one et compose pyrrolidine-2-one condense avec un heterocycle aromatique |
| KR100944301B1 (ko) | 2005-02-22 | 2010-02-24 | 더 리젠츠 오브 더 유니버시티 오브 미시간 | Mdm2의 소분자 억제제 및 이의 용도 |
| US7576082B2 (en) | 2005-06-24 | 2009-08-18 | Hoffman-La Roche Inc. | Oxindole derivatives |
| AU2007224452A1 (en) | 2006-03-13 | 2007-09-20 | F. Hoffmann-La Roche Ag | Spiroindolinone derivatives |
| US20070213341A1 (en) | 2006-03-13 | 2007-09-13 | Li Chen | Spiroindolinone derivatives |
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| BRPI0713119A2 (pt) | 2006-06-30 | 2012-04-17 | Schering Corp | piperidinas substituìdas que aumentam a atividade de p53 e os usos destas |
| US7737174B2 (en) * | 2006-08-30 | 2010-06-15 | The Regents Of The University Of Michigan | Indole inhibitors of MDM2 and the uses thereof |
| CA2661354C (fr) | 2006-08-30 | 2012-12-18 | The Regents Of The University Of Michigan | Nouvelles petites molecules inhibitrices de mdm2 et leurs utilisations |
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| SG184288A1 (en) * | 2010-04-09 | 2012-11-29 | Univ Michigan | Biomarkers for mdm2 inhibitors for use in treating disease |
-
2010
- 2010-11-04 US US12/939,234 patent/US8088815B2/en not_active Expired - Fee Related
- 2010-11-29 JP JP2012541424A patent/JP5647262B2/ja not_active Expired - Fee Related
- 2010-11-29 CN CN201080062931.4A patent/CN102741257B/zh not_active Expired - Fee Related
- 2010-11-29 AU AU2010326855A patent/AU2010326855B2/en not_active Ceased
- 2010-11-29 TW TW099141297A patent/TW201129571A/zh unknown
- 2010-11-29 EP EP10793189.1A patent/EP2507243B1/fr not_active Not-in-force
- 2010-11-29 BR BR112012012872A patent/BR112012012872A2/pt not_active Application Discontinuation
- 2010-11-29 NZ NZ600024A patent/NZ600024A/en not_active IP Right Cessation
- 2010-11-29 PH PH1/2012/501029A patent/PH12012501029A1/en unknown
- 2010-11-29 MX MX2012006260A patent/MX2012006260A/es active IP Right Grant
- 2010-11-29 SG SG2012040341A patent/SG181465A1/en unknown
- 2010-11-29 WO PCT/EP2010/068353 patent/WO2011067185A1/fr not_active Ceased
- 2010-11-29 ES ES10793189.1T patent/ES2543468T3/es active Active
- 2010-11-29 MY MYPI2012002434A patent/MY160596A/en unknown
- 2010-11-29 KR KR1020127016926A patent/KR101418191B1/ko not_active Expired - Fee Related
- 2010-11-29 RU RU2012125763/04A patent/RU2571100C2/ru not_active IP Right Cessation
- 2010-11-29 MA MA34939A patent/MA33976B1/fr unknown
- 2010-11-29 CA CA2781823A patent/CA2781823A1/fr not_active Abandoned
- 2010-11-29 PE PE2012000748A patent/PE20121334A1/es not_active Application Discontinuation
- 2010-11-30 AR ARP100104410A patent/AR079226A1/es unknown
-
2012
- 2012-05-18 CR CR20120259A patent/CR20120259A/es unknown
- 2012-05-24 IL IL220010A patent/IL220010A/en not_active IP Right Cessation
- 2012-05-24 CO CO12086101A patent/CO6541606A2/es not_active Application Discontinuation
- 2012-05-30 CL CL2012001405A patent/CL2012001405A1/es unknown
- 2012-06-01 ZA ZA2012/04036A patent/ZA201204036B/en unknown
- 2012-06-01 EC ECSP12011945 patent/ECSP12011945A/es unknown
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