DE60318321T2 - Pyrazolopyridine als hemmstoffe cyclin abhängiger kinasen - Google Patents
Pyrazolopyridine als hemmstoffe cyclin abhängiger kinasen Download PDFInfo
- Publication number
- DE60318321T2 DE60318321T2 DE60318321T DE60318321T DE60318321T2 DE 60318321 T2 DE60318321 T2 DE 60318321T2 DE 60318321 T DE60318321 T DE 60318321T DE 60318321 T DE60318321 T DE 60318321T DE 60318321 T2 DE60318321 T2 DE 60318321T2
- Authority
- DE
- Germany
- Prior art keywords
- alkyl
- aryl
- group
- heteroaryl
- cycloalkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 0 *c1c(c(*)c(*)c(*)c2N=*)[n]2nc1 Chemical compound *c1c(c(*)c(*)c(*)c2N=*)[n]2nc1 0.000 description 3
- UZOFELREXGAFOI-UHFFFAOYSA-N CC1CCNCC1 Chemical compound CC1CCNCC1 UZOFELREXGAFOI-UHFFFAOYSA-N 0.000 description 1
- IFRQUYKKCFSYPQ-UHFFFAOYSA-N CNC1=CCN(C)CC1 Chemical compound CNC1=CCN(C)CC1 IFRQUYKKCFSYPQ-UHFFFAOYSA-N 0.000 description 1
- NFOFCRCQFQTYPD-UHFFFAOYSA-N C[Sc]C1CCNCC1 Chemical compound C[Sc]C1CCNCC1 NFOFCRCQFQTYPD-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
-
- 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)
- Hematology (AREA)
- Oncology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US41213802P | 2002-09-19 | 2002-09-19 | |
| US412138P | 2002-09-19 | ||
| PCT/US2003/029841 WO2004026872A1 (en) | 2002-09-19 | 2003-09-17 | Pyrazolopyridines as cyclin dependent kinase inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE60318321D1 DE60318321D1 (en) | 2008-02-07 |
| DE60318321T2 true DE60318321T2 (de) | 2008-12-11 |
Family
ID=32030811
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE60318321T Expired - Lifetime DE60318321T2 (de) | 2002-09-19 | 2003-09-17 | Pyrazolopyridine als hemmstoffe cyclin abhängiger kinasen |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US7151104B2 (enExample) |
| EP (1) | EP1539750B1 (enExample) |
| JP (1) | JP4845380B2 (enExample) |
| KR (1) | KR20050072090A (enExample) |
| CN (1) | CN100475812C (enExample) |
| AR (1) | AR041292A1 (enExample) |
| AT (1) | ATE382048T1 (enExample) |
| AU (1) | AU2003270846B2 (enExample) |
| CA (1) | CA2499593C (enExample) |
| DE (1) | DE60318321T2 (enExample) |
| ES (1) | ES2297203T3 (enExample) |
| IL (1) | IL167432A (enExample) |
| MX (1) | MXPA05003059A (enExample) |
| MY (1) | MY136840A (enExample) |
| NZ (1) | NZ538595A (enExample) |
| TW (1) | TWI283243B (enExample) |
| WO (1) | WO2004026872A1 (enExample) |
| ZA (1) | ZA200502271B (enExample) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4579351B2 (ja) | 1996-12-03 | 2010-11-10 | スローン−ケッタリング インスティトュート フォア キャンサー リサーチ | エポチロンの合成とその中間体及びその類似物並びにその使用 |
| US20020058286A1 (en) * | 1999-02-24 | 2002-05-16 | Danishefsky Samuel J. | Synthesis of epothilones, intermediates thereto and analogues thereof |
| US6921769B2 (en) | 2002-08-23 | 2005-07-26 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto and analogues thereof |
| CA2496477C (en) | 2002-08-23 | 2012-10-16 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto, analogues and uses thereof |
| US7649006B2 (en) | 2002-08-23 | 2010-01-19 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto and analogues thereof |
| JP5117189B2 (ja) * | 2004-08-27 | 2013-01-09 | サイクラセル リミテッド | プリン及びピリミジンcdk阻害剤、並びに自己免疫疾患の治療のためのそれらの使用 |
| JP5106098B2 (ja) * | 2005-02-28 | 2012-12-26 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | スルホンアミド化合物の抗癌剤との新規併用 |
| US20090047278A1 (en) * | 2005-02-28 | 2009-02-19 | Eisai R & D Management Co., Ltd. | Novel Combinational Use of Sulfonamide Compound |
| US7304074B2 (en) * | 2005-04-05 | 2007-12-04 | Hoffmann-La Roche Inc. | Substituted 1,5-naphthyridine azolinones |
| KR20080002935A (ko) * | 2005-04-07 | 2008-01-04 | 데이진 화-마 가부시키가이샤 | 피라졸로[1,5-a]피리딘 유도체 또는 그 의학상 허용되는염 |
| US7417053B2 (en) | 2005-04-07 | 2008-08-26 | Teijin Pharma Limited | Pyrazolo[1,5-a]pyridine derivatives or pharmaceutically acceptable salts thereof |
| CN101300233A (zh) | 2005-09-09 | 2008-11-05 | 先灵公司 | 氮杂稠合的细胞周期蛋白依赖性激酶抑制剂 |
| KR20090094336A (ko) * | 2006-11-27 | 2009-09-04 | 하. 룬트벡 아크티에 셀스카브 | 헤테로아릴 아미드 유도체 |
| KR20090031122A (ko) * | 2007-09-21 | 2009-03-25 | 주식회사 중외제약 | 인다졸 골격을 함유하는 화합물, 이의 제조방법 및 상기화합물을 함유하는 약제학적 조성물 |
| FR2940284B1 (fr) * | 2008-12-19 | 2011-02-18 | Sanofi Aventis | Derives de 6-cycloamino-2,3-di-pyridinyl-imidazo°1,2-b!- pyridazine,leur preparation et leur application en therapeutique |
| US8883819B2 (en) | 2011-09-01 | 2014-11-11 | Irm Llc | Bicyclic heterocycle derivatives for the treatment of pulmonary arterial hypertension |
| US9073921B2 (en) | 2013-03-01 | 2015-07-07 | Novartis Ag | Salt forms of bicyclic heterocyclic derivatives |
| AU2016243529B2 (en) * | 2015-03-27 | 2021-03-25 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinases |
| EP3377908B1 (en) | 2015-11-18 | 2020-08-05 | Genzyme Corporation | Biomarker of polycystic kidney disease and uses thereof |
| CN109790160B (zh) * | 2016-09-07 | 2022-11-15 | 上海海和药物研究开发股份有限公司 | 吡啶并五元芳香环类化合物、其制备方法及用途 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7091346B1 (en) | 1995-11-01 | 2006-08-15 | Novartis Ag | Purine derivatives and processes for their preparation |
| ES2281941T3 (es) | 1997-12-13 | 2007-10-01 | Bristol-Myers Squibb Company | Uso de pirazolo(3,4-b)piridina como inhibidores de quinasa dependiente de ciclina. |
| SE9802794D0 (sv) * | 1998-08-21 | 1998-08-21 | Astra Ab | New compounds |
| FR2801308B1 (fr) * | 1999-11-19 | 2003-05-09 | Oreal | COMPOSITIONS DE TEINTURE DE FIBRES KERATINIQUES CONTENANT DE DES 3-AMINO PYRAZOLO-[1,(-a]-PYRIDINES, PROCEDE DE TEINTURE, NOUVELLES 3-AMINO PYRAZOLO-[1,5-a]-PYRIDINES |
| CN100356979C (zh) * | 2000-02-03 | 2007-12-26 | 卫材R&D管理有限公司 | 整联蛋白表达抑制剂 |
| WO2002050079A1 (fr) * | 2000-12-20 | 2002-06-27 | Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R.A.S.) | Inhibiteurs de kinases dependantes des cylines (cdk) et de la glycogene synthase kinase-3 (gsk-3) |
| CZ20032398A3 (cs) * | 2001-03-08 | 2004-02-18 | Astrazeneca Ab | Nové použití derivátů 6-karboxamidoimidazo [1,2-a] pyridinu |
| CN1202896C (zh) * | 2002-02-07 | 2005-05-25 | 北京燕化高新技术股份有限公司 | 空气分离时纯化空气的方法 |
-
2003
- 2003-09-17 AT AT03752559T patent/ATE382048T1/de not_active IP Right Cessation
- 2003-09-17 CN CNB038220113A patent/CN100475812C/zh not_active Expired - Fee Related
- 2003-09-17 AU AU2003270846A patent/AU2003270846B2/en not_active Ceased
- 2003-09-17 KR KR1020057004435A patent/KR20050072090A/ko not_active Abandoned
- 2003-09-17 CA CA2499593A patent/CA2499593C/en not_active Expired - Fee Related
- 2003-09-17 EP EP03752559A patent/EP1539750B1/en not_active Expired - Lifetime
- 2003-09-17 ES ES03752559T patent/ES2297203T3/es not_active Expired - Lifetime
- 2003-09-17 DE DE60318321T patent/DE60318321T2/de not_active Expired - Lifetime
- 2003-09-17 AR ARP030103374A patent/AR041292A1/es active IP Right Grant
- 2003-09-17 NZ NZ538595A patent/NZ538595A/en not_active IP Right Cessation
- 2003-09-17 TW TW092125613A patent/TWI283243B/zh not_active IP Right Cessation
- 2003-09-17 MX MXPA05003059A patent/MXPA05003059A/es active IP Right Grant
- 2003-09-17 WO PCT/US2003/029841 patent/WO2004026872A1/en not_active Ceased
- 2003-09-17 MY MYPI20033535A patent/MY136840A/en unknown
- 2003-09-17 JP JP2004538405A patent/JP4845380B2/ja not_active Expired - Fee Related
- 2003-09-17 US US10/664,337 patent/US7151104B2/en not_active Expired - Lifetime
-
2005
- 2005-03-15 IL IL167432A patent/IL167432A/en not_active IP Right Cessation
- 2005-03-17 ZA ZA200502271A patent/ZA200502271B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ES2297203T3 (es) | 2008-05-01 |
| CA2499593C (en) | 2011-08-16 |
| TWI283243B (en) | 2007-07-01 |
| CN1681816A (zh) | 2005-10-12 |
| NZ538595A (en) | 2006-04-28 |
| CA2499593A1 (en) | 2004-04-01 |
| HK1071758A1 (en) | 2005-07-29 |
| IL167432A (en) | 2010-05-17 |
| ZA200502271B (en) | 2005-09-19 |
| EP1539750B1 (en) | 2007-12-26 |
| JP2006503060A (ja) | 2006-01-26 |
| KR20050072090A (ko) | 2005-07-08 |
| JP4845380B2 (ja) | 2011-12-28 |
| AU2003270846B2 (en) | 2006-11-23 |
| ATE382048T1 (de) | 2008-01-15 |
| DE60318321D1 (en) | 2008-02-07 |
| MXPA05003059A (es) | 2005-05-27 |
| AU2003270846A1 (en) | 2004-04-08 |
| AR041292A1 (es) | 2005-05-11 |
| EP1539750A1 (en) | 2005-06-15 |
| CN100475812C (zh) | 2009-04-08 |
| US20040097516A1 (en) | 2004-05-20 |
| MY136840A (en) | 2008-11-28 |
| US7151104B2 (en) | 2006-12-19 |
| WO2004026872A1 (en) | 2004-04-01 |
| TW200409775A (en) | 2004-06-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8364 | No opposition during term of opposition |