TW200730502A - Isoquinoline aminopyrazole derivatives, their manufacture and use as pharmaceutical agents - Google Patents
Isoquinoline aminopyrazole derivatives, their manufacture and use as pharmaceutical agentsInfo
- Publication number
- TW200730502A TW200730502A TW095146990A TW95146990A TW200730502A TW 200730502 A TW200730502 A TW 200730502A TW 095146990 A TW095146990 A TW 095146990A TW 95146990 A TW95146990 A TW 95146990A TW 200730502 A TW200730502 A TW 200730502A
- Authority
- TW
- Taiwan
- Prior art keywords
- manufacture
- isoquinoline
- pharmaceutical agents
- aminopyrazole derivatives
- compounds
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—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
- C07D401/02—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 two hetero rings
- C07D401/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—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
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP05027720 | 2005-12-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
TW200730502A true TW200730502A (en) | 2007-08-16 |
Family
ID=36337671
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TW095146990A TW200730502A (en) | 2005-12-19 | 2006-12-15 | Isoquinoline aminopyrazole derivatives, their manufacture and use as pharmaceutical agents |
Country Status (15)
Country | Link |
---|---|
US (1) | US7572809B2 (zh) |
EP (1) | EP1966190A1 (zh) |
JP (1) | JP2009519918A (zh) |
KR (1) | KR20080076963A (zh) |
CN (1) | CN101341145A (zh) |
AR (1) | AR058362A1 (zh) |
AU (1) | AU2006328997A1 (zh) |
BR (1) | BRPI0620012A2 (zh) |
CA (1) | CA2633101A1 (zh) |
IL (1) | IL191984A0 (zh) |
NO (1) | NO20082643L (zh) |
RU (1) | RU2008129381A (zh) |
TW (1) | TW200730502A (zh) |
WO (1) | WO2007071348A1 (zh) |
ZA (1) | ZA200805163B (zh) |
Families Citing this family (47)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PL1846394T3 (pl) | 2005-02-04 | 2012-04-30 | Astrazeneca Ab | Pochodne pirazoliloaminopirydyny użyteczne jako inhibitory kinazy |
JP2008081492A (ja) * | 2006-08-31 | 2008-04-10 | Banyu Pharmaceut Co Ltd | 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 |
EA201070143A1 (ru) * | 2007-07-13 | 2010-08-30 | Аддекс Фарма С.А. | Новые гетероароматические производные и их использование в качестве положительных аллостерических модуляторов метаботропных глутаматных рецепторов |
WO2009010871A2 (en) * | 2007-07-13 | 2009-01-22 | Addex Pharma S.A. | Pyrazole derivatives as antagonists of adenosine a3 receptor |
JP5209254B2 (ja) * | 2007-08-30 | 2013-06-12 | 日本曹達株式会社 | 置換フェノキシアザビシクロオクタン誘導体の製造方法 |
US8193182B2 (en) | 2008-01-04 | 2012-06-05 | Intellikine, Inc. | Substituted isoquinolin-1(2H)-ones, and methods of use thereof |
NZ587051A (en) | 2008-01-04 | 2012-12-21 | Intellikine Llc | Isoquinolinone derivatives, compositions and methods of inhibiting phosphatidyl inositol-3 kinase (pi3 kinase) |
US8703778B2 (en) | 2008-09-26 | 2014-04-22 | Intellikine Llc | Heterocyclic kinase inhibitors |
CA2760791C (en) | 2009-05-07 | 2017-06-20 | Intellikine, Inc. | Heterocyclic compounds and uses thereof |
US8258149B2 (en) * | 2009-05-08 | 2012-09-04 | Hoffmann-La Roche Inc. | Isoquinoline derivatives |
ES2593256T3 (es) | 2010-05-21 | 2016-12-07 | Infinity Pharmaceuticals, Inc. | Compuestos químicos, composiciones y métodos para las modulaciones de cinasas |
US20130296363A1 (en) * | 2010-09-01 | 2013-11-07 | Ambit Biosciences Corporation | Quinoline and isoquinoline derivatives for use as jak modulators |
EP2441755A1 (en) * | 2010-09-30 | 2012-04-18 | Almirall, S.A. | Pyridine- and isoquinoline-derivatives as Syk and JAK kinase inhibitors |
WO2012064973A2 (en) | 2010-11-10 | 2012-05-18 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
KR20130129244A (ko) * | 2010-12-17 | 2013-11-27 | 에프. 호프만-라 로슈 아게 | 치환된 6,6-융합된 질소 헤테로환형 화합물 및 이의 용도 |
CN103648499B (zh) | 2011-01-10 | 2017-02-15 | 无限药品股份有限公司 | 用于制备异喹啉酮的方法及异喹啉酮的固体形式 |
ES2543050T3 (es) | 2011-02-28 | 2015-08-14 | Array Biopharma, Inc. | Inhibidores de serina/treonina quinasa |
CA2842190A1 (en) | 2011-07-19 | 2013-01-24 | Infinity Pharmaceuticals Inc. | Heterocyclic compounds and uses thereof |
EP2734520B1 (en) | 2011-07-19 | 2016-09-14 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
US9187462B2 (en) | 2011-08-04 | 2015-11-17 | Array Biopharma Inc. | Substituted quinazolines as serine/threonine kinase inhibitors |
WO2013032591A1 (en) | 2011-08-29 | 2013-03-07 | Infinity Pharmaceuticals Inc. | Heterocyclic compounds and uses thereof |
SI2820009T1 (en) | 2012-03-01 | 2018-05-31 | Array Biopharma, Inc. | Serine / Threonine kinase inhibitors |
US8940742B2 (en) | 2012-04-10 | 2015-01-27 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
US8828998B2 (en) | 2012-06-25 | 2014-09-09 | Infinity Pharmaceuticals, Inc. | Treatment of lupus, fibrotic conditions, and inflammatory myopathies and other disorders using PI3 kinase inhibitors |
BR112015004548A2 (pt) * | 2012-08-27 | 2017-08-08 | Array Biopharma Inc | inibidores de serina/treonina para tratamento de doenças hiperproliferativas |
JO3377B1 (ar) * | 2013-03-11 | 2019-03-13 | Takeda Pharmaceuticals Co | مشتقات بيريدينيل وبيريدينيل مندمج |
US9481667B2 (en) | 2013-03-15 | 2016-11-01 | Infinity Pharmaceuticals, Inc. | Salts and solid forms of isoquinolinones and composition comprising and methods of using the same |
WO2015051241A1 (en) | 2013-10-04 | 2015-04-09 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
CA2925944C (en) | 2013-10-04 | 2023-01-10 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
EP4066834A1 (en) | 2014-03-19 | 2022-10-05 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds for use in the treatment of pi3k-gamma mediated disorders |
LT3536685T (lt) | 2014-04-04 | 2022-04-25 | Pfizer Inc. | Biciklinio sulieto heteroarilo arba arilo junginiai ir jų naudojimas kaip irak4 inhibitorių |
WO2015160975A2 (en) | 2014-04-16 | 2015-10-22 | Infinity Pharmaceuticals, Inc. | Combination therapies |
CN103922965B (zh) * | 2014-04-28 | 2016-08-24 | 西安瑞联新材料股份有限公司 | 一种4-甲氧基-2-甲基苯乙腈的合成方法 |
WO2016054491A1 (en) | 2014-10-03 | 2016-04-07 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
EP3303348B1 (en) * | 2015-05-28 | 2019-08-07 | Theravance Biopharma R&D IP, LLC | Naphthyridine compounds as jak kinase inhibitors |
CN108349985A (zh) | 2015-09-14 | 2018-07-31 | 无限药品股份有限公司 | 异喹啉酮的固体形式、其制备方法、包含其的组合物及其使用方法 |
US10759806B2 (en) | 2016-03-17 | 2020-09-01 | Infinity Pharmaceuticals, Inc. | Isotopologues of isoquinolinone and quinazolinone compounds and uses thereof as PI3K kinase inhibitors |
US10919914B2 (en) | 2016-06-08 | 2021-02-16 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
WO2017223422A1 (en) | 2016-06-24 | 2017-12-28 | Infinity Pharmaceuticals, Inc. | Combination therapies |
PE20200008A1 (es) | 2017-03-30 | 2020-01-06 | Hoffmann La Roche | Isoquinolinas como inhibidores de hpk1 |
AR112027A1 (es) | 2017-06-15 | 2019-09-11 | Biocryst Pharm Inc | Inhibidores de alk 2 quinasa que contienen imidazol |
US11612606B2 (en) | 2018-10-03 | 2023-03-28 | Genentech, Inc. | 8-aminoisoquinoline compounds and uses thereof |
CA3154247A1 (en) * | 2019-10-25 | 2021-04-29 | Mitchell H. KEYLOR | N-(heteroaryl) quinazolin-2-amine derivatives as lrrk2 inhibitors, pharmaceutical compositions, and uses thereof |
CN111039940B (zh) * | 2019-12-31 | 2022-10-21 | 北京鑫开元医药科技有限公司 | 一种Aurora A激酶抑制剂、制备方法、药物组合物及其用途 |
WO2022235492A1 (en) * | 2021-05-04 | 2022-11-10 | Board Of Regents, The University Of Texas System | Indanone and tetralone-keto or hydroxyl oximes as cancer therapeutics |
FR3132098A1 (fr) | 2022-01-25 | 2023-07-28 | Rhodia Operations | Procédé de préparation d’acide p-hydroxycinnamiques |
CN114573506B (zh) * | 2022-03-21 | 2022-09-30 | 邦恩泰(山东)生物医药科技集团股份有限公司 | 药物中间体及合成方法、异喹啉类衍生物及其合成方法 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
UA71945C2 (en) | 1999-01-27 | 2005-01-17 | Pfizer Prod Inc | Substituted bicyclic derivatives being used as anticancer agents |
ATE309241T1 (de) * | 1999-09-10 | 2005-11-15 | Merck & Co Inc | Tyrosin kinase inhibitoren |
AP2001002266A0 (en) * | 2000-08-31 | 2001-09-30 | Pfizer Prod Inc | Pyrazole derivatives. |
US20050209297A1 (en) * | 2000-08-31 | 2005-09-22 | Pfizer Inc | Pyrazole derivatives |
CA2422371C (en) | 2000-09-15 | 2010-05-18 | Vertex Pharmaceuticals Incorporated | Pyrazole compounds useful as protein kinase inhibitors |
US20030105090A1 (en) | 2000-12-21 | 2003-06-05 | David Bebbington | Pyrazole compounds useful as protein kinase inhibitors |
ATE339418T1 (de) | 2001-06-01 | 2006-10-15 | Vertex Pharma | Thiazolverbindungen, die sich als inhibitoren von proteinkinasen eignen |
TWI372050B (en) | 2003-07-03 | 2012-09-11 | Astex Therapeutics Ltd | (morpholin-4-ylmethyl-1h-benzimidazol-2-yl)-1h-pyrazoles |
MXPA06013042A (es) * | 2004-05-14 | 2007-02-12 | Millennium Pharm Inc | Compuestos y m??todos para inhibir la progresion mit??tica. |
GB0509227D0 (en) * | 2005-05-05 | 2005-06-15 | Chroma Therapeutics Ltd | Intracellular enzyme inhibitors |
-
2006
- 2006-12-12 US US11/637,733 patent/US7572809B2/en not_active Expired - Fee Related
- 2006-12-15 CA CA002633101A patent/CA2633101A1/en not_active Abandoned
- 2006-12-15 WO PCT/EP2006/012112 patent/WO2007071348A1/en active Application Filing
- 2006-12-15 EP EP06840991A patent/EP1966190A1/en not_active Withdrawn
- 2006-12-15 AR ARP060105558A patent/AR058362A1/es unknown
- 2006-12-15 KR KR1020087014869A patent/KR20080076963A/ko not_active Application Discontinuation
- 2006-12-15 AU AU2006328997A patent/AU2006328997A1/en not_active Abandoned
- 2006-12-15 JP JP2008544887A patent/JP2009519918A/ja active Pending
- 2006-12-15 TW TW095146990A patent/TW200730502A/zh unknown
- 2006-12-15 CN CNA2006800480407A patent/CN101341145A/zh active Pending
- 2006-12-15 RU RU2008129381/04A patent/RU2008129381A/ru not_active Application Discontinuation
- 2006-12-15 BR BRPI0620012-5A patent/BRPI0620012A2/pt not_active Application Discontinuation
-
2008
- 2008-06-05 NO NO20082643A patent/NO20082643L/no not_active Application Discontinuation
- 2008-06-05 IL IL191984A patent/IL191984A0/en unknown
- 2008-06-12 ZA ZA200805163A patent/ZA200805163B/xx unknown
Also Published As
Publication number | Publication date |
---|---|
KR20080076963A (ko) | 2008-08-20 |
IL191984A0 (en) | 2008-12-29 |
RU2008129381A (ru) | 2010-01-27 |
NO20082643L (no) | 2008-09-01 |
BRPI0620012A2 (pt) | 2011-10-25 |
AR058362A1 (es) | 2008-01-30 |
CA2633101A1 (en) | 2007-06-28 |
ZA200805163B (en) | 2009-06-24 |
US20070179151A1 (en) | 2007-08-02 |
WO2007071348A1 (en) | 2007-06-28 |
US7572809B2 (en) | 2009-08-11 |
EP1966190A1 (en) | 2008-09-10 |
JP2009519918A (ja) | 2009-05-21 |
CN101341145A (zh) | 2009-01-07 |
AU2006328997A1 (en) | 2007-06-28 |
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