JP2004509115A - プロテインキナーゼインヒビターとして有用なピラゾール化合物 - Google Patents
プロテインキナーゼインヒビターとして有用なピラゾール化合物 Download PDFInfo
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- JP2004509115A JP2004509115A JP2002526858A JP2002526858A JP2004509115A JP 2004509115 A JP2004509115 A JP 2004509115A JP 2002526858 A JP2002526858 A JP 2002526858A JP 2002526858 A JP2002526858 A JP 2002526858A JP 2004509115 A JP2004509115 A JP 2004509115A
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- Prior art keywords
- ring
- aliphatic
- optionally substituted
- halo
- phenyl
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- 0 CC([*+]=C(c1c(*)cc[s]1)NC)=I Chemical compound CC([*+]=C(c1c(*)cc[s]1)NC)=I 0.000 description 54
- PTKYZFPNSHUICN-UHFFFAOYSA-N CC(C)C(C1C(N)N=CCC1)N Chemical compound CC(C)C(C1C(N)N=CCC1)N PTKYZFPNSHUICN-UHFFFAOYSA-N 0.000 description 1
- AJMLHVYIEZYKIB-UHFFFAOYSA-N CC(C1C(NC(CC2)NC(C)C2=N)=NC(C(C=CCC2)=C2C(F)(F)F)NC1C(CC1)CCC1N)NC Chemical compound CC(C1C(NC(CC2)NC(C)C2=N)=NC(C(C=CCC2)=C2C(F)(F)F)NC1C(CC1)CCC1N)NC AJMLHVYIEZYKIB-UHFFFAOYSA-N 0.000 description 1
- CIZPNYVIGQXKPR-UHFFFAOYSA-N CC(NC(CC1)CCC1c1c(C)c(NC(c2ccccc2N)=N)nc(-c2c(C(F)(F)F)cccc2)n1)=O Chemical compound CC(NC(CC1)CCC1c1c(C)c(NC(c2ccccc2N)=N)nc(-c2c(C(F)(F)F)cccc2)n1)=O CIZPNYVIGQXKPR-UHFFFAOYSA-N 0.000 description 1
- DOSKTRRKJNRBGI-UHFFFAOYSA-N CC1=Nc2c1cccc2 Chemical compound CC1=Nc2c1cccc2 DOSKTRRKJNRBGI-UHFFFAOYSA-N 0.000 description 1
- RHXNSSPPMRSIQF-UHFFFAOYSA-N CC1C(C)C=C(Nc2nc(-c3cc(C(F)(F)F)cc(C(F)(F)F)c3)nc3c2cccc3)N(C)C1 Chemical compound CC1C(C)C=C(Nc2nc(-c3cc(C(F)(F)F)cc(C(F)(F)F)c3)nc3c2cccc3)N(C)C1 RHXNSSPPMRSIQF-UHFFFAOYSA-N 0.000 description 1
- QUPLTULZRMCAPW-UHFFFAOYSA-N CC1c(cccc2)c2C(Nc2nc(-c(cccc3)c3Cl)nc(N3CCNCC3)c2C)=C(C)CC1 Chemical compound CC1c(cccc2)c2C(Nc2nc(-c(cccc3)c3Cl)nc(N3CCNCC3)c2C)=C(C)CC1 QUPLTULZRMCAPW-UHFFFAOYSA-N 0.000 description 1
- WQVHDUCJOJFSRR-UHFFFAOYSA-N CCC(CC1)C(C)C=C1Nc1nc(-c2cccc(N)c2)nc2ccccc12 Chemical compound CCC(CC1)C(C)C=C1Nc1nc(-c2cccc(N)c2)nc2ccccc12 WQVHDUCJOJFSRR-UHFFFAOYSA-N 0.000 description 1
- VVFUCXCAQWCFLH-NGQTVDHRSA-N CC[C@H](C)/C=C(\NC)/NC1=NC(c2cccc(C(F)(F)F)c2)[N-]c2c1cccc2 Chemical compound CC[C@H](C)/C=C(\NC)/NC1=NC(c2cccc(C(F)(F)F)c2)[N-]c2c1cccc2 VVFUCXCAQWCFLH-NGQTVDHRSA-N 0.000 description 1
- HBNLBFIEWGOOBJ-UHFFFAOYSA-N Cc1c(C)nc(-c(cccc2)c2Cl)nc1N Chemical compound Cc1c(C)nc(-c(cccc2)c2Cl)nc1N HBNLBFIEWGOOBJ-UHFFFAOYSA-N 0.000 description 1
- PXBFMLJZNCDSMP-UHFFFAOYSA-N NC(c(cccc1)c1N)=O Chemical compound NC(c(cccc1)c1N)=O PXBFMLJZNCDSMP-UHFFFAOYSA-N 0.000 description 1
- NEBILHRHTHIIQV-UHFFFAOYSA-N Nc1c(CCNC2)c2nc(-c2c(C(F)(F)F)cccc2)n1 Chemical compound Nc1c(CCNC2)c2nc(-c2c(C(F)(F)F)cccc2)n1 NEBILHRHTHIIQV-UHFFFAOYSA-N 0.000 description 1
- CEMMDFSMYNZKBR-UHFFFAOYSA-N Nc1nc(-c(cccc2)c2Cl)nc2c1CCCCC2 Chemical compound Nc1nc(-c(cccc2)c2Cl)nc2c1CCCCC2 CEMMDFSMYNZKBR-UHFFFAOYSA-N 0.000 description 1
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- 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
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- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- Chemical & Material Sciences (AREA)
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- Diabetes (AREA)
- Immunology (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Biomedical Technology (AREA)
- Obesity (AREA)
- Pulmonology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Psychiatry (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Emergency Medicine (AREA)
- Oncology (AREA)
- Vascular Medicine (AREA)
- Transplantation (AREA)
- Communicable Diseases (AREA)
- Virology (AREA)
- Hospice & Palliative Care (AREA)
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Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US23279500P | 2000-09-15 | 2000-09-15 | |
| US25788700P | 2000-12-21 | 2000-12-21 | |
| US28694901P | 2001-04-27 | 2001-04-27 | |
| PCT/US2001/028793 WO2002022605A1 (en) | 2000-09-15 | 2001-09-14 | Pyrazole compounds useful as protein kinase inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2004509115A true JP2004509115A (ja) | 2004-03-25 |
| JP2004509115A5 JP2004509115A5 (cg-RX-API-DMAC7.html) | 2005-04-28 |
Family
ID=27398347
Family Applications (9)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002526858A Pending JP2004509115A (ja) | 2000-09-15 | 2001-09-14 | プロテインキナーゼインヒビターとして有用なピラゾール化合物 |
| JP2002526857A Expired - Fee Related JP4105948B2 (ja) | 2000-09-15 | 2001-09-14 | プロテインキナーゼインヒビターとして有用なピラゾール化合物 |
| JP2002526856A Expired - Fee Related JP4922539B2 (ja) | 2000-09-15 | 2001-09-14 | プロテインキナーゼインヒビターとして有用なピラゾール化合物 |
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Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006043490A1 (ja) * | 2004-10-20 | 2006-04-27 | Astellas Pharma Inc. | 非芳香環縮合ピリミジン誘導体 |
| US7947690B2 (en) | 2004-10-20 | 2011-05-24 | Astellas Pharma Inc. | Pyrimidine derivative condensed with a non-aromatic ring |
| JP2008520713A (ja) * | 2004-11-17 | 2008-06-19 | ミイカナ セラピューティクス インコーポレイテッド | キナーゼ阻害剤 |
| JP2008537536A (ja) * | 2005-01-26 | 2008-09-18 | シェーリング コーポレイション | 癌の処置のためのプロテインキナーゼインヒビターとしての、3−(インダゾール−5−イル)−(1,2,4)トリアジン誘導体、および関連する化合物 |
| JP2010520889A (ja) * | 2007-03-09 | 2010-06-17 | バーテックス ファーマシューティカルズ インコーポレイテッド | 蛋白キナーゼの阻害剤として有用なアミノピリミジン |
| JP2012521425A (ja) * | 2009-03-23 | 2012-09-13 | Msd株式会社 | オーロラa選択的阻害作用を有する新規アミノピリジン誘導体 |
| JP2012521427A (ja) * | 2009-03-24 | 2012-09-13 | Msd株式会社 | オーロラa選択的阻害作用を有する新規アミノピリジン誘導体 |
| JP2012521426A (ja) * | 2009-03-24 | 2012-09-13 | Msd株式会社 | オーロラa選択的阻害作用を有する新規アミノピリジン誘導体 |
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