MXPA05009611A - Piperidinas sustituidas como nuevos inhibidores de mdm2-p53. - Google Patents
Piperidinas sustituidas como nuevos inhibidores de mdm2-p53.Info
- Publication number
- MXPA05009611A MXPA05009611A MXPA05009611A MXPA05009611A MXPA05009611A MX PA05009611 A MXPA05009611 A MX PA05009611A MX PA05009611 A MXPA05009611 A MX PA05009611A MX PA05009611 A MXPA05009611 A MX PA05009611A MX PA05009611 A MXPA05009611 A MX PA05009611A
- Authority
- MX
- Mexico
- Prior art keywords
- inhibitors
- formula
- substituted piperidines
- iii
- pharmaceutically acceptable
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title 1
- 150000003053 piperidines Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 239000003937 drug carrier Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 239000000546 pharmaceutical excipient Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/40—Oxygen atoms
- C07D211/44—Oxygen atoms attached in position 4
- C07D211/52—Oxygen atoms attached in position 4 having an aryl radical as the second substituent in position 4
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/451—Non condensed piperidines, e.g. piperocaine having a carbocyclic group directly attached to the heterocyclic ring, e.g. glutethimide, meperidine, loperamide, phencyclidine, piminodine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/92—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with a hetero atom directly attached to the ring nitrogen atom
- C07D211/96—Sulfur atom
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)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
La presente invencion proporciona compuestos que tienen la formula (II) o la formula (III) y las sales farmaceuticamente aceptables de los mismos, en donde X, n y R1-R12 son como se definen en la presente. La invencion tambien proporciona una composicion farmaceutica que comprende una cantidad terapeuticamente efectiva de un compuesto representado por la formula (II) o (III) y un vehiculo o excipiente farmaceuticamente aceptable. Los compuestos son utiles para el tratamiento de cancer.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US45438703P | 2003-03-13 | 2003-03-13 | |
| PCT/EP2004/002339 WO2004080460A1 (en) | 2003-03-13 | 2004-03-08 | SUBSTITUTED PIPERIDINES AS NOVEL MDM2-p53 INHIBITORS |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MXPA05009611A true MXPA05009611A (es) | 2005-10-18 |
Family
ID=32990900
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MXPA05009611A MXPA05009611A (es) | 2003-03-13 | 2004-03-08 | Piperidinas sustituidas como nuevos inhibidores de mdm2-p53. |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US6916833B2 (es) |
| EP (1) | EP1605941A1 (es) |
| JP (1) | JP4468897B2 (es) |
| KR (1) | KR100755767B1 (es) |
| CN (1) | CN100372837C (es) |
| AU (1) | AU2004218842B2 (es) |
| BR (1) | BRPI0408338A (es) |
| CA (1) | CA2516145A1 (es) |
| MX (1) | MXPA05009611A (es) |
| RU (1) | RU2333201C2 (es) |
| WO (1) | WO2004080460A1 (es) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2009000132A (es) * | 2006-06-30 | 2009-01-26 | Schering Corp | Metodo para el uso de piperidinas sustituidas que incrementan la actividad de p53. |
| CN101595107A (zh) | 2006-06-30 | 2009-12-02 | 先灵公司 | 能提高p53活性的有取代哌啶及其用途 |
| JPWO2008072655A1 (ja) | 2006-12-14 | 2010-04-02 | 第一三共株式会社 | イミダゾチアゾール誘導体 |
| JPWO2009151069A1 (ja) | 2008-06-12 | 2011-11-17 | 第一三共株式会社 | 4,7−ジアザスピロ[2.5]オクタン環構造を有するイミダゾチアゾール誘導体 |
| KR20120013403A (ko) * | 2009-04-22 | 2012-02-14 | 액시킨 파마수티컬스 인코포레이티드 | 2,5-이치환된 아릴설폰아마이드 ccr3 길항제 |
| US8859776B2 (en) | 2009-10-14 | 2014-10-14 | Merck Sharp & Dohme Corp. | Substituted piperidines that increase p53 activity and the uses thereof |
| WO2011060049A2 (en) | 2009-11-12 | 2011-05-19 | The Regents Of The University Of Michigan | Spiro-oxindole mdm2 antagonists |
| US10159669B2 (en) * | 2010-03-02 | 2018-12-25 | Ian H. Chan | Individual and combination of mdivi-1 and nutlin-3 for topical or intravitreal ophthalmic use |
| JO2998B1 (ar) * | 2010-06-04 | 2016-09-05 | Amgen Inc | مشتقات بيبيريدينون كمثبطات mdm2 لعلاج السرطان |
| FR2967072B1 (fr) | 2010-11-05 | 2013-03-29 | Univ Dundee | Procede pour ameliorer la production de virus et semences vaccinales influenza |
| EP2638046A4 (en) | 2010-11-12 | 2014-06-25 | Univ Michigan | SPIRO-oxindole-MDM2 ANTAGONISTS |
| CN103717605B (zh) | 2011-05-11 | 2016-05-18 | 密执安州立大学董事会 | 螺-羟吲哚mdm2拮抗剂 |
| WO2013062923A1 (en) | 2011-10-28 | 2013-05-02 | Merck Sharp & Dohme Corp. | MACROCYCLES THAT INCREASE p53 ACTIVITY AND THE USES THEREOF |
| WO2013096150A1 (en) | 2011-12-21 | 2013-06-27 | Merck Sharp & Dohme Corp. | Substituted piperidines as hdm2 inhibitors |
| KR102196882B1 (ko) | 2012-12-20 | 2020-12-30 | 머크 샤프 앤드 돔 코포레이션 | Hdm2 억제제로서의 치환된 이미다조피리딘 |
| US9540377B2 (en) | 2013-01-30 | 2017-01-10 | Merck Sharp & Dohme Corp. | 2,6,7,8 substituted purines as HDM2 inhibitors |
| JOP20200296A1 (ar) * | 2013-06-10 | 2017-06-16 | Amgen Inc | عمليات صنع وأشكال بلورية من mdm2 مثبط |
| KR101851270B1 (ko) * | 2015-07-10 | 2018-04-25 | 고려대학교 산학협력단 | 자연 살해세포의 대량증식 방법 및 배양용 조성물 |
| CN109311900A (zh) | 2016-04-06 | 2019-02-05 | 密执安大学评议会 | 用于配体依赖性靶蛋白质降解的单官能中间体 |
| KR102387316B1 (ko) | 2016-04-06 | 2022-04-15 | 더 리젠츠 오브 더 유니버시티 오브 미시간 | Mdm2 단백질 분해제 |
| ES2858151T3 (es) | 2016-05-20 | 2021-09-29 | Hoffmann La Roche | Conjugados de PROTAC-anticuerpo y procedimientos de uso |
| CN108088727B (zh) | 2016-11-21 | 2020-07-07 | 中国科学院大连化学物理研究所 | 一种离体体液中蛋白质的预处理方法 |
| EP3863720A1 (en) | 2018-10-08 | 2021-08-18 | The Regents Of The University Of Michigan | Small molecule mdm2 protein degraders |
| EP4121043A4 (en) | 2020-03-19 | 2024-07-24 | Kymera Therapeutics, Inc. | Mdm2 degraders and uses thereof |
| WO2023056069A1 (en) | 2021-09-30 | 2023-04-06 | Angiex, Inc. | Degrader-antibody conjugates and methods of using same |
| WO2024240858A1 (en) | 2023-05-23 | 2024-11-28 | Valerio Therapeutics | Protac molecules directed against dna damage repair system and uses thereof |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4286095A (en) * | 1976-08-05 | 1981-08-25 | Canada Packers Inc. | 4-Arylpiperidine derivatives |
| SE7708555L (sv) * | 1976-08-05 | 1978-02-06 | Delmar Chem | 4-arylpiperidinderivat och forfarande for framstellning derav |
| SE9400447D0 (sv) * | 1994-02-11 | 1994-02-11 | Astra Ab | New compounds |
| US6274735B1 (en) * | 1998-08-10 | 2001-08-14 | Hoffmann-La Roche Inc. | Process and intermediates for preparation of substituted piperidines |
| GB9819860D0 (en) | 1998-09-12 | 1998-11-04 | Zeneca Ltd | Chemical compounds |
| GB9912961D0 (en) * | 1999-06-03 | 1999-08-04 | Pfizer Ltd | Metalloprotease inhibitors |
-
2004
- 2004-03-04 US US10/793,296 patent/US6916833B2/en not_active Expired - Fee Related
- 2004-03-08 CN CNB2004800066874A patent/CN100372837C/zh not_active Expired - Fee Related
- 2004-03-08 EP EP04718272A patent/EP1605941A1/en not_active Withdrawn
- 2004-03-08 RU RU2005131501/04A patent/RU2333201C2/ru not_active IP Right Cessation
- 2004-03-08 CA CA002516145A patent/CA2516145A1/en not_active Abandoned
- 2004-03-08 MX MXPA05009611A patent/MXPA05009611A/es active IP Right Grant
- 2004-03-08 JP JP2005518673A patent/JP4468897B2/ja not_active Expired - Lifetime
- 2004-03-08 AU AU2004218842A patent/AU2004218842B2/en not_active Ceased
- 2004-03-08 BR BRPI0408338-5A patent/BRPI0408338A/pt not_active IP Right Cessation
- 2004-03-08 WO PCT/EP2004/002339 patent/WO2004080460A1/en not_active Ceased
- 2004-03-08 KR KR1020057016661A patent/KR100755767B1/ko not_active Expired - Fee Related
-
2005
- 2005-03-18 US US11/083,750 patent/US7060713B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CN100372837C (zh) | 2008-03-05 |
| US6916833B2 (en) | 2005-07-12 |
| CA2516145A1 (en) | 2004-09-23 |
| RU2005131501A (ru) | 2006-05-27 |
| AU2004218842B2 (en) | 2009-11-12 |
| US20040180929A1 (en) | 2004-09-16 |
| KR20050106505A (ko) | 2005-11-09 |
| US20050171157A1 (en) | 2005-08-04 |
| RU2333201C2 (ru) | 2008-09-10 |
| JP4468897B2 (ja) | 2010-05-26 |
| AU2004218842A1 (en) | 2004-09-23 |
| EP1605941A1 (en) | 2005-12-21 |
| BRPI0408338A (pt) | 2006-03-21 |
| US7060713B2 (en) | 2006-06-13 |
| WO2004080460A1 (en) | 2004-09-23 |
| KR100755767B1 (ko) | 2007-09-10 |
| JP2006519767A (ja) | 2006-08-31 |
| CN1758909A (zh) | 2006-04-12 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant or registration |