MA34732B1 - Spiro-oxindoles antagonistes de mdm2 - Google Patents
Spiro-oxindoles antagonistes de mdm2Info
- Publication number
- MA34732B1 MA34732B1 MA36005A MA36005A MA34732B1 MA 34732 B1 MA34732 B1 MA 34732B1 MA 36005 A MA36005 A MA 36005A MA 36005 A MA36005 A MA 36005A MA 34732 B1 MA34732 B1 MA 34732B1
- Authority
- MA
- Morocco
- Prior art keywords
- oxindoles
- mdm2
- spiro
- antagonists
- compounds
- Prior art date
Links
- 102000012199 E3 ubiquitin-protein ligase Mdm2 Human genes 0.000 title abstract 2
- 108050002772 E3 ubiquitin-protein ligase Mdm2 Proteins 0.000 title abstract 2
- 239000005557 antagonist Substances 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 230000003993 interaction Effects 0.000 abstract 1
- 229940124597 therapeutic agent Drugs 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N5/00—Radiation therapy
- A61N5/10—X-ray therapy; Gamma-ray therapy; Particle-irradiation therapy
-
- 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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Radiology & Medical Imaging (AREA)
- Pathology (AREA)
- Oncology (AREA)
- Dermatology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
La présente invention concerne des composés, des compositions, et des procédés dans le domaine de la chimie médicinale. Les composés et compositions présentement décrits concernent des spiro-oxindoles qui ont une fonction d'antagonistes de l'interaction entre p53 et MDM2, et leur utilisation en tant qu'agents thérapeutiques pour le traitement du cancer et d'autres maladies.
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US41309410P | 2010-11-12 | 2010-11-12 | |
| US201161451968P | 2011-03-11 | 2011-03-11 | |
| US201161451958P | 2011-03-11 | 2011-03-11 | |
| US201161470992P | 2011-04-01 | 2011-04-01 | |
| PCT/US2011/060300 WO2012065022A2 (fr) | 2010-11-12 | 2011-11-11 | Spiro-oxindoles antagonistes de mdm2 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA34732B1 true MA34732B1 (fr) | 2013-12-03 |
Family
ID=46048358
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA36005A MA34732B1 (fr) | 2010-11-12 | 2013-06-10 | Spiro-oxindoles antagonistes de mdm2 |
Country Status (27)
| Country | Link |
|---|---|
| US (2) | US8680132B2 (fr) |
| EP (1) | EP2638046A4 (fr) |
| JP (1) | JP2014500870A (fr) |
| KR (1) | KR101929188B1 (fr) |
| CN (1) | CN103298818B (fr) |
| AR (1) | AR083849A1 (fr) |
| AU (1) | AU2011326395B2 (fr) |
| CA (1) | CA2817585A1 (fr) |
| CO (1) | CO6721010A2 (fr) |
| CR (1) | CR20130271A (fr) |
| DO (1) | DOP2013000104A (fr) |
| EA (1) | EA201390682A1 (fr) |
| EC (1) | ECSP13012678A (fr) |
| GT (1) | GT201300118A (fr) |
| IL (1) | IL226275A0 (fr) |
| MA (1) | MA34732B1 (fr) |
| MX (1) | MX2013005238A (fr) |
| NI (1) | NI201300041A (fr) |
| NZ (1) | NZ611866A (fr) |
| PE (1) | PE20140408A1 (fr) |
| PH (1) | PH12013500955A1 (fr) |
| SG (1) | SG190230A1 (fr) |
| TW (1) | TWI535723B (fr) |
| UA (1) | UA109464C2 (fr) |
| UY (1) | UY33725A (fr) |
| WO (1) | WO2012065022A2 (fr) |
| ZA (1) | ZA201304042B (fr) |
Families Citing this family (65)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7759383B2 (en) | 2005-02-22 | 2010-07-20 | The Regents Of The University Of Michigan | Small molecule inhibitors of MDM2 and the uses thereof |
| WO2008095063A1 (fr) | 2007-01-31 | 2008-08-07 | Dana-Farber Cancer Institute, Inc. | Peptides p53 stabilisés et utilisations de ceux-ci |
| ES2430067T3 (es) | 2007-03-28 | 2013-11-18 | President And Fellows Of Harvard College | Polipéptidos cosidos |
| AU2010319595B2 (en) * | 2009-11-12 | 2015-09-17 | The Regents Of The University Of Michigan | Spiro-oxindole MDM2 antagonists |
| US8440693B2 (en) | 2009-12-22 | 2013-05-14 | Novartis Ag | Substituted isoquinolinones and quinazolinones |
| DK2603600T3 (da) | 2010-08-13 | 2019-03-04 | Aileron Therapeutics Inc | Peptidomimetiske makrocyklusser |
| CA2829188C (fr) | 2011-03-10 | 2016-10-18 | Daiichi Sankyo Company, Limited | Derive de dispiropyrrolidine |
| ES2624808T3 (es) | 2011-05-11 | 2017-07-17 | The Regents Of The University Of Michigan | Antagonistas de MDM2 espirooxindólicos |
| CA2852468A1 (fr) | 2011-10-18 | 2013-04-25 | Aileron Therapeutics, Inc. | Macrocycles peptidomimetiques |
| SG10201606775YA (en) | 2012-02-15 | 2016-10-28 | Aileron Therapeutics Inc | Peptidomimetic macrocycles |
| HK1205454A1 (en) | 2012-02-15 | 2015-12-18 | Aileron Therapeutics, Inc. | Triazole-crosslinked and thioether-crosslinked peptidomimetic macrocycles |
| US8993614B2 (en) | 2012-03-15 | 2015-03-31 | F. Hoffmann-La Roche Ag | Substituted pyrrolidine-2-carboxamides |
| US9365576B2 (en) | 2012-05-24 | 2016-06-14 | Novartis Ag | Pyrrolopyrrolidinone compounds |
| CA2887285A1 (fr) | 2012-11-01 | 2014-05-08 | Aileron Therapeutics, Inc. | Acides amines disubstitues et procedes de preparation et d'utilisation de ceux-ci |
| TW201429969A (zh) | 2012-12-20 | 2014-08-01 | Merck Sharp & Dohme | 作爲hdm2抑制劑之經取代咪唑吡啶 |
| EP2752191A1 (fr) * | 2013-01-07 | 2014-07-09 | Sanofi | Compositions et procédés utilisant un antagoniste de hdm2 et un inhibiteur de mek |
| US9403827B2 (en) | 2013-01-22 | 2016-08-02 | Novartis Ag | Substituted purinone compounds |
| US9556180B2 (en) | 2013-01-22 | 2017-01-31 | Novartis Ag | Pyrazolo[3,4-d]pyrimidinone compounds as inhibitors of the P53/MDM2 interaction |
| EA029312B1 (ru) | 2013-05-27 | 2018-03-30 | Новартис Аг | Производные имидазопирролидинона и их применение при лечении заболеваний |
| ES2650562T3 (es) | 2013-05-28 | 2018-01-19 | Novartis Ag | Derivados de pirazolo-pirrolidin-4-ona y su uso en el tratamiento de enfermedades |
| PL3004108T3 (pl) | 2013-05-28 | 2018-03-30 | Novartis Ag | Pochodne pirazolo-pirolidyn-4-onu jako inhibitory BET oraz ich zastosowanie w leczeniu chorób |
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| WO2015161032A1 (fr) | 2014-04-17 | 2015-10-22 | The Regents Of The University Of Michigan | Inhibiteurs de hdac et méthodes thérapeutiques les utilisant |
| TW201613576A (en) | 2014-06-26 | 2016-04-16 | Novartis Ag | Intermittent dosing of MDM2 inhibitor |
| JP6503386B2 (ja) | 2014-07-03 | 2019-04-17 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | MDM2−p53阻害剤としての新しいスピロ[3H−インドール−3,2’−ピロリジン]−2(1H)−オン化合物および誘導体 |
| CN105829318B (zh) | 2014-08-18 | 2018-10-02 | 哈德森生物医药有限公司 | 作为mdm2抑制剂的螺吡咯烷 |
| KR20170042779A (ko) | 2014-08-21 | 2017-04-19 | 베링거 인겔하임 인터내셔날 게엠베하 | Mdm2-p53 억제제로서의 신규 스피로[3h-인돌-3,2'-피롤리딘]-2(1h)-온 화합물 및 유도체 |
| SG10201902598VA (en) | 2014-09-24 | 2019-04-29 | Aileron Therapeutics Inc | Peptidomimetic macrocycles and formulations thereof |
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| JP2018516844A (ja) | 2015-03-20 | 2018-06-28 | エルロン・セラピューティクス・インコーポレイテッドAileron Therapeutics,Inc. | ペプチド模倣大環状分子およびその使用 |
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| PL3359542T3 (pl) | 2015-10-09 | 2021-09-20 | Boehringer Ingelheim International Gmbh | Związki i pochodne spiro[3h-indolo-3,2’-pirolidyno]-2(1h)-onowe jako inhibitory mdm2-p53 |
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-
2011
- 2011-11-11 JP JP2013538923A patent/JP2014500870A/ja not_active Ceased
- 2011-11-11 AR ARP110104223A patent/AR083849A1/es unknown
- 2011-11-11 US US13/294,315 patent/US8680132B2/en not_active Expired - Fee Related
- 2011-11-11 KR KR1020137015168A patent/KR101929188B1/ko not_active Expired - Fee Related
- 2011-11-11 PE PE2013001063A patent/PE20140408A1/es not_active Application Discontinuation
- 2011-11-11 CA CA2817585A patent/CA2817585A1/fr not_active Abandoned
- 2011-11-11 EA EA201390682A patent/EA201390682A1/ru unknown
- 2011-11-11 CN CN201180064853.6A patent/CN103298818B/zh not_active Expired - Fee Related
- 2011-11-11 AU AU2011326395A patent/AU2011326395B2/en not_active Ceased
- 2011-11-11 TW TW100141225A patent/TWI535723B/zh not_active IP Right Cessation
- 2011-11-11 PH PH1/2013/500955A patent/PH12013500955A1/en unknown
- 2011-11-11 SG SG2013035894A patent/SG190230A1/en unknown
- 2011-11-11 UY UY0001033725A patent/UY33725A/es not_active Application Discontinuation
- 2011-11-11 EP EP11840490.4A patent/EP2638046A4/fr not_active Withdrawn
- 2011-11-11 UA UAA201307447A patent/UA109464C2/uk unknown
- 2011-11-11 MX MX2013005238A patent/MX2013005238A/es active IP Right Grant
- 2011-11-11 WO PCT/US2011/060300 patent/WO2012065022A2/fr not_active Ceased
- 2011-11-11 NZ NZ61186611A patent/NZ611866A/en not_active IP Right Cessation
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- 2013-05-10 DO DO2013000104A patent/DOP2013000104A/es unknown
- 2013-06-02 EC ECSP13012678 patent/ECSP13012678A/es unknown
- 2013-06-03 ZA ZA2013/04042A patent/ZA201304042B/en unknown
- 2013-06-07 CR CR20130271A patent/CR20130271A/es unknown
- 2013-06-10 MA MA36005A patent/MA34732B1/fr unknown
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