JP2010508288A - キナーゼ阻害剤として有用なヘテロサイクリックアミド化合物 - Google Patents
キナーゼ阻害剤として有用なヘテロサイクリックアミド化合物 Download PDFInfo
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- JP2010508288A JP2010508288A JP2009534850A JP2009534850A JP2010508288A JP 2010508288 A JP2010508288 A JP 2010508288A JP 2009534850 A JP2009534850 A JP 2009534850A JP 2009534850 A JP2009534850 A JP 2009534850A JP 2010508288 A JP2010508288 A JP 2010508288A
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- 0 Cc1c(C(Nc2cc(C(N*)=O)ccc2C)=O)[n]c(CN2*)c1C2=O Chemical compound Cc1c(C(Nc2cc(C(N*)=O)ccc2C)=O)[n]c(CN2*)c1C2=O 0.000 description 9
- YLYIGLFJQOHNLD-UHFFFAOYSA-N COc(cc1)cc(OC)c1C(N1CCNCC1)=O Chemical compound COc(cc1)cc(OC)c1C(N1CCNCC1)=O YLYIGLFJQOHNLD-UHFFFAOYSA-N 0.000 description 1
- HNHMMWBURNQSHP-UHFFFAOYSA-N C[n]1c2cc(N)ccc2c(C#N)c1 Chemical compound C[n]1c2cc(N)ccc2c(C#N)c1 HNHMMWBURNQSHP-UHFFFAOYSA-N 0.000 description 1
- YAKYJNFAHDIXEU-UHFFFAOYSA-N Cc(c(NC(C(C=C(C)N1)=CC1=O)=O)c1)ccc1C(NC1CC1)=O Chemical compound Cc(c(NC(C(C=C(C)N1)=CC1=O)=O)c1)ccc1C(NC1CC1)=O YAKYJNFAHDIXEU-UHFFFAOYSA-N 0.000 description 1
- JHJVAKBKNABYPA-UHFFFAOYSA-N Cc(c(NC(c([s]c(-c(cc1)ccc1Cl)c1)c1N)=O)c1)ccc1C(NC1CC1)=O Chemical compound Cc(c(NC(c([s]c(-c(cc1)ccc1Cl)c1)c1N)=O)c1)ccc1C(NC1CC1)=O JHJVAKBKNABYPA-UHFFFAOYSA-N 0.000 description 1
- AEWMYJNRMDLLRT-UHFFFAOYSA-N Cc(c(NC(c1c[s]c(-c2cnccc2)c1)=O)c1)ccc1C(NC1CC1)=O Chemical compound Cc(c(NC(c1c[s]c(-c2cnccc2)c1)=O)c1)ccc1C(NC1CC1)=O AEWMYJNRMDLLRT-UHFFFAOYSA-N 0.000 description 1
- QMVNNYMSPMSVOL-UHFFFAOYSA-N Cc(c(NC(c1cc(Br)c[s]1)=O)c1)ccc1C(NC1CC1)=O Chemical compound Cc(c(NC(c1cc(Br)c[s]1)=O)c1)ccc1C(NC1CC1)=O QMVNNYMSPMSVOL-UHFFFAOYSA-N 0.000 description 1
- FWZYXQGOOFWPLV-UHFFFAOYSA-N Cc(c(NC(c1ccc(-c(cc2)ccc2C(NC)=O)[s]1)=O)c1)ccc1C(NC1CC1)=O Chemical compound Cc(c(NC(c1ccc(-c(cc2)ccc2C(NC)=O)[s]1)=O)c1)ccc1C(NC1CC1)=O FWZYXQGOOFWPLV-UHFFFAOYSA-N 0.000 description 1
- NLHDHFYSDUQEGA-UHFFFAOYSA-N Cc(c(NC(c1ccc(-c2cc(C(NC3CC3)=O)ccc2)[s]1)=O)c1)ccc1C(NC1CC1)=O Chemical compound Cc(c(NC(c1ccc(-c2cc(C(NC3CC3)=O)ccc2)[s]1)=O)c1)ccc1C(NC1CC1)=O NLHDHFYSDUQEGA-UHFFFAOYSA-N 0.000 description 1
- BOYHXHQUTNXTNI-UHFFFAOYSA-N Cc(c(NC(c1ccc(-c2ncccc2C(F)(F)F)[s]1)=O)c1)ccc1C(NC1CC1)=O Chemical compound Cc(c(NC(c1ccc(-c2ncccc2C(F)(F)F)[s]1)=O)c1)ccc1C(NC1CC1)=O BOYHXHQUTNXTNI-UHFFFAOYSA-N 0.000 description 1
- INIMRKBPUZALDM-UHFFFAOYSA-N Cc(c(NC(c1cnc(C(c2ccccc2)=O)[n]1C)=O)c1)ccc1C(NC1CC1)=O Chemical compound Cc(c(NC(c1cnc(C(c2ccccc2)=O)[n]1C)=O)c1)ccc1C(NC1CC1)=O INIMRKBPUZALDM-UHFFFAOYSA-N 0.000 description 1
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- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more 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
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- 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
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
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- Physical Education & Sports Medicine (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
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- Urology & Nephrology (AREA)
- Transplantation (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Furan Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyrrole Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US85490806P | 2006-10-27 | 2006-10-27 | |
| PCT/US2007/082471 WO2008057775A2 (en) | 2006-10-27 | 2007-10-25 | Heterocyclic amide compounds useful as kinase inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2010508288A true JP2010508288A (ja) | 2010-03-18 |
| JP2010508288A5 JP2010508288A5 (enExample) | 2010-10-21 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009534850A Withdrawn JP2010508288A (ja) | 2006-10-27 | 2007-10-25 | キナーゼ阻害剤として有用なヘテロサイクリックアミド化合物 |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US7935696B2 (enExample) |
| EP (2) | EP2083816A2 (enExample) |
| JP (1) | JP2010508288A (enExample) |
| CN (1) | CN101616667A (enExample) |
| NO (1) | NO20091590L (enExample) |
| WO (1) | WO2008057775A2 (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2013535434A (ja) * | 2010-07-15 | 2013-09-12 | バイエル・インテレクチユアル・プロパテイー・ゲー・エム・ベー・ハー | 有害生物防除剤としての新規複素環式化合物 |
| WO2013161871A1 (ja) * | 2012-04-25 | 2013-10-31 | 興和株式会社 | Tlr阻害作用を有するチオフェン誘導体 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7935696B2 (en) * | 2006-10-27 | 2011-05-03 | Bristol-Myers Squibb Company | Heterocyclic amide compounds useful as kinase inhibitors |
| AU2009244664A1 (en) | 2008-04-04 | 2009-11-12 | Gilead Sciences, Inc. | Triazolopyridinone derivatives for use as stearoyl CoA desaturase inhibitors |
| CA2719362A1 (en) * | 2008-04-04 | 2009-10-08 | Gilead Sciences, Inc. | Pyrrolotriazinone derivatives for use as stearoyl coa desaturase inhibitors |
| ES2383340T3 (es) * | 2008-09-02 | 2012-06-20 | Boehringer Ingelheim International Gmbh | Derivados de (fenil)-amida del ácido 7-(piperazin-1-ilmetil)-1H-indol-2-carboxílico y compuestos relacionados en calidad de inhibidores de MAP-QUINASA P38 para el tratamiento de enfermedades de las vías respiratorias. |
| CN102203064A (zh) | 2008-09-02 | 2011-09-28 | 贝林格尔.英格海姆国际有限公司 | 新的苯甲酰胺,其制备及其作为药物的用途 |
| US8580959B2 (en) * | 2008-10-08 | 2013-11-12 | Bristol-Myers Squibb Company | Azolotriazinone melanin concentrating hormone receptor-1 antagonists |
| WO2010071583A1 (en) * | 2008-12-18 | 2010-06-24 | Astrazeneca Ab | Pharmaceutical product comprising a p38 kinase inhibitor and a second active ingredient |
| WO2010071885A1 (en) | 2008-12-19 | 2010-06-24 | Cephalon, Inc. | Pyrrolotriazines as alk and jak2 inhibitors |
| EA018907B1 (ru) * | 2009-01-30 | 2013-11-29 | ГЛЭКСОСМИТКЛАЙН ЭлЭлСи | Кристаллический гидрохлорид n-{(1s)-2-амино-1-[(3-фторфенил)метил]этил}-5-хлор-4-(4-хлор-1-метил-1h-пиразол-5-ил)-2-тиофенкарбоксамида |
| US8889674B2 (en) | 2009-03-05 | 2014-11-18 | Shionogi & Co., Ltd. | Piperidine and pyrrolidine derivatives having NPY Y5 receptor antagonism |
| CA2777723C (en) * | 2009-12-14 | 2016-06-21 | Novartis Ag | Methods for making silicone hydrogel lenses from water-based lens formulations |
| US8765797B2 (en) | 2010-06-21 | 2014-07-01 | Board Of Regents, The University Of Texas System | TG2 inhibitors and uses thereof |
| US20130269064A1 (en) * | 2010-11-23 | 2013-10-10 | Syngenta Participations Ag | Insecticidal compounds |
| MA42038A (fr) * | 2015-05-05 | 2018-03-14 | Bayer Pharma AG | Dérivés de cyclohexane à substitution amido |
| US10287291B2 (en) * | 2016-08-19 | 2019-05-14 | Bristol-Myers Squibb Company | Seco-cyclopropapyrroloindole compounds, antibody-drug conjugates thereof, and methods of making and use |
| CN111233734B (zh) * | 2019-12-06 | 2023-09-19 | 济宁医学院 | 一种芳氧基马来酰亚胺化合物及其制备方法 |
| CN114656414B (zh) * | 2022-05-24 | 2022-08-23 | 常熟华虞环境科技有限公司 | 三氮唑改性二氧化钛光催化剂及其制备方法 |
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| US4200750A (en) | 1977-01-07 | 1980-04-29 | Westwood Pharmaceuticals Inc. | 4-Substituted imidazo [1,2-a]quinoxalines |
| GB9816837D0 (en) * | 1998-08-04 | 1998-09-30 | Zeneca Ltd | Amide derivatives |
| IL118544A (en) | 1995-06-07 | 2001-08-08 | Smithkline Beecham Corp | History of imidazole, the process for their preparation and the pharmaceutical preparations containing them |
| JP2000503302A (ja) | 1996-01-11 | 2000-03-21 | スミスクライン・ビーチャム・コーポレイション | 新規置換イミダゾール化合物 |
| US5945418A (en) | 1996-12-18 | 1999-08-31 | Vertex Pharmaceuticals Incorporated | Inhibitors of p38 |
| US6147080A (en) | 1996-12-18 | 2000-11-14 | Vertex Pharmaceuticals Incorporated | Inhibitors of p38 |
| US6087496A (en) | 1998-05-22 | 2000-07-11 | G. D. Searle & Co. | Substituted pyrazoles suitable as p38 kinase inhibitors |
| CN1264376A (zh) | 1997-05-22 | 2000-08-23 | G·D·瑟尔公司 | 作为p38激酶抑制剂的3(5)-杂芳基取代的吡唑化合物 |
| EP1019396A1 (en) | 1997-07-02 | 2000-07-19 | SmithKline Beecham Corporation | Novel cycloalkyl substituted imidazoles |
| US6130235A (en) | 1998-05-22 | 2000-10-10 | Scios Inc. | Compounds and methods to treat cardiac failure and other disorders |
| US6184226B1 (en) | 1998-08-28 | 2001-02-06 | Scios Inc. | Quinazoline derivatives as inhibitors of P-38 α |
| CA2342251A1 (en) | 1998-08-28 | 2000-03-09 | Scios Inc. | Use of piperidines and/or piperazines as inhibitors of p38-alpha kinase |
| KR20010110668A (ko) * | 1999-03-17 | 2001-12-13 | 다비드 에 질레스 | 아미드 유도체 |
| GB9906566D0 (en) | 1999-03-23 | 1999-05-19 | Zeneca Ltd | Chemical compounds |
| GB9924092D0 (en) | 1999-10-13 | 1999-12-15 | Zeneca Ltd | Pyrimidine derivatives |
| BR0007447A (pt) | 1999-11-10 | 2002-04-09 | Ortho Mcneil Pharm Inc | 2-aril-3-(heteroaril)-imidazo[1,2-a]pirimidinas substituìdas, composições farmacêuticas e métodos |
| WO2002014308A1 (en) | 2000-08-17 | 2002-02-21 | Eli Lilly And Company | Antithrombotic agents |
| GB0124936D0 (en) | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
| GB0124928D0 (en) * | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
| WO2004071440A2 (en) | 2003-02-06 | 2004-08-26 | Bristol-Myers Squibb Company | Thiazolyl-based compounds useful as kinase inhibitors |
| GB0308511D0 (en) * | 2003-04-14 | 2003-05-21 | Astex Technology Ltd | Pharmaceutical compounds |
| BRPI0409949A (pt) * | 2003-05-01 | 2006-04-25 | Bristol Myers Squibb Co | compostos de pirazol amida aril-substituìda úteis como inibidores de cinase |
| US7419978B2 (en) * | 2003-10-22 | 2008-09-02 | Bristol-Myers Squibb Company | Phenyl-aniline substituted bicyclic compounds useful as kinase inhibitors |
| GB0329572D0 (en) | 2003-12-20 | 2004-01-28 | Astrazeneca Ab | Amide derivatives |
| EP1714958B9 (en) * | 2004-01-28 | 2017-05-31 | Mitsui Chemicals Agro, Inc. | Amide derivatives, process for production of the same, and method for application thereof as insecticide |
| US7652146B2 (en) * | 2004-02-06 | 2010-01-26 | Bristol-Myers Squibb Company | Process for preparing 2-aminothiazole-5-carboxamides useful as kinase inhibitors |
| JP2007532615A (ja) * | 2004-04-13 | 2007-11-15 | アステックス、セラピューティックス、リミテッド | 医薬化合物 |
| US20090105218A1 (en) * | 2004-05-29 | 2009-04-23 | 7Tm Pharma A/S | CRTH2 Receptor Ligands For Therapeutic Use |
| AU2005317870A1 (en) * | 2004-12-22 | 2006-06-29 | Astrazeneca Ab | Pyridine carboxamide derivatives for use as anticancer agents |
| TW200635899A (en) | 2004-12-22 | 2006-10-16 | Astrazeneca Ab | Chemical compounds |
| CA2599989A1 (en) * | 2005-03-03 | 2006-09-08 | Sirtris Pharmaceuticals, Inc. | N-phenyl benzamide derivatives as sirtuin modulators |
| AU2006260299B8 (en) * | 2005-06-21 | 2012-11-29 | Mitsui Chemicals, Inc. | Amide derivative and insecticide containing the same |
| US7935696B2 (en) * | 2006-10-27 | 2011-05-03 | Bristol-Myers Squibb Company | Heterocyclic amide compounds useful as kinase inhibitors |
| US7943658B2 (en) * | 2007-07-23 | 2011-05-17 | Bristol-Myers Squibb Company | Indole indane amide compounds useful as CB2 agonists and method |
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2007
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- 2007-10-25 WO PCT/US2007/082471 patent/WO2008057775A2/en not_active Ceased
- 2007-10-25 JP JP2009534850A patent/JP2010508288A/ja not_active Withdrawn
- 2007-10-25 EP EP07863490A patent/EP2083816A2/en not_active Withdrawn
- 2007-10-25 EP EP12156082.5A patent/EP2468717B1/en not_active Not-in-force
- 2007-10-25 CN CN200780048839A patent/CN101616667A/zh active Pending
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2009
- 2009-04-22 NO NO20091590A patent/NO20091590L/no not_active Application Discontinuation
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2011
- 2011-03-02 US US13/038,488 patent/US8404689B2/en active Active
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2013535434A (ja) * | 2010-07-15 | 2013-09-12 | バイエル・インテレクチユアル・プロパテイー・ゲー・エム・ベー・ハー | 有害生物防除剤としての新規複素環式化合物 |
| WO2013161871A1 (ja) * | 2012-04-25 | 2013-10-31 | 興和株式会社 | Tlr阻害作用を有するチオフェン誘導体 |
Also Published As
| Publication number | Publication date |
|---|---|
| CN101616667A (zh) | 2009-12-30 |
| NO20091590L (no) | 2009-05-08 |
| EP2468717A1 (en) | 2012-06-27 |
| EP2468717B1 (en) | 2013-11-20 |
| US8404689B2 (en) | 2013-03-26 |
| EP2083816A2 (en) | 2009-08-05 |
| WO2008057775A3 (en) | 2008-07-31 |
| US20110160207A1 (en) | 2011-06-30 |
| US20080171741A1 (en) | 2008-07-17 |
| US7935696B2 (en) | 2011-05-03 |
| WO2008057775A2 (en) | 2008-05-15 |
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