MX340402B - Inhibidores triciclicos de cinasas. - Google Patents
Inhibidores triciclicos de cinasas.Info
- Publication number
- MX340402B MX340402B MX2013009873A MX2013009873A MX340402B MX 340402 B MX340402 B MX 340402B MX 2013009873 A MX2013009873 A MX 2013009873A MX 2013009873 A MX2013009873 A MX 2013009873A MX 340402 B MX340402 B MX 340402B
- Authority
- MX
- Mexico
- Prior art keywords
- kinases
- tricyclic inhibitors
- compounds
- relates
- present
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- 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
- C07D487/12—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 three hetero rings
- C07D487/14—Ortho-condensed systems
-
- 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
Abstract
La presente invención se refiere a compuestos de fórmula (I) o sus sales farmacéuticamente aceptables, en donde X, Y, Z, R3 y R4 se definen en la descripción. La presente invención también se refiere a composiciones que contienen dichos compuestos que son útiles para inhibir cinasas tales como wee-1 y métodos de tratamiento de enfermedades como el cáncer.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161447405P | 2011-02-28 | 2011-02-28 | |
PCT/US2012/026685 WO2012161812A1 (en) | 2011-02-28 | 2012-02-27 | Tricyclic inhibitors of kinases |
Publications (2)
Publication Number | Publication Date |
---|---|
MX2013009873A MX2013009873A (es) | 2014-03-12 |
MX340402B true MX340402B (es) | 2016-07-07 |
Family
ID=46000328
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2013009873A MX340402B (es) | 2011-02-28 | 2012-02-27 | Inhibidores triciclicos de cinasas. |
Country Status (11)
Country | Link |
---|---|
US (1) | US8710065B2 (es) |
EP (1) | EP2681221B1 (es) |
JP (1) | JP5886326B2 (es) |
CN (1) | CN103703005A (es) |
AR (1) | AR085502A1 (es) |
CA (1) | CA2827648A1 (es) |
ES (1) | ES2587514T3 (es) |
MX (1) | MX340402B (es) |
TW (1) | TWI532742B (es) |
UY (1) | UY33925A (es) |
WO (1) | WO2012161812A1 (es) |
Families Citing this family (50)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8754114B2 (en) | 2010-12-22 | 2014-06-17 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3 |
UA117347C2 (uk) | 2012-06-13 | 2018-07-25 | Інсайт Холдинґс Корпорейшн | Заміщені трициклічні сполуки як інгібітори fgfr |
WO2014026125A1 (en) | 2012-08-10 | 2014-02-13 | Incyte Corporation | Pyrazine derivatives as fgfr inhibitors |
US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
CN105263931B (zh) | 2013-04-19 | 2019-01-25 | 因赛特公司 | 作为fgfr抑制剂的双环杂环 |
JPWO2015029447A1 (ja) * | 2013-08-30 | 2017-03-02 | 興和株式会社 | 光学活性カルビノール化合物の製造方法 |
GB201322602D0 (en) * | 2013-12-19 | 2014-02-05 | Almac Discovery Ltd | Pharmaceutical compounds |
US10300055B2 (en) | 2014-04-10 | 2019-05-28 | Dalhousie University | Treatment of parkinson's disease through ARFGAP1 inhibition |
EP3185860A4 (en) | 2014-08-29 | 2018-08-29 | The Board of Regents of the University of Texas System | Novel capsazepine analogs for the treatment of cancer and other proliferative diseases |
US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
WO2016134294A1 (en) | 2015-02-20 | 2016-08-25 | Incyte Corporation | Bicyclic heterocycles as fgfr4 inhibitors |
MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
UA121669C2 (uk) | 2015-02-20 | 2020-07-10 | Інсайт Корпорейшн | Біциклічні гетероцикли як інгібітори fgfr |
AU2017359844B2 (en) | 2016-11-16 | 2021-09-30 | Impact Therapeutics (Shanghai), Inc | 8,9-dihydroimidazole[1,2-a]pyrimido[5,4-e]pyrimidine-5(6H)-ketone compound |
CN110198943B (zh) * | 2017-01-23 | 2021-04-16 | 石家庄智康弘仁新药开发有限公司 | 作为Wee1抑制剂的1,2-二氢-3H-吡唑[3,4-d]嘧啶-3-酮衍生物 |
EP3600247A1 (en) | 2017-03-31 | 2020-02-05 | Seattle Genetics, Inc. | Combinations of chk1- and wee1 - inhibitors |
AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
US11345710B2 (en) | 2017-07-10 | 2022-05-31 | Impact Therapeutics (Shanghai), Inc | Imidazo[1,2-b]pyrimido[4,5-d]pyridazin-5(6H)-ones and the use thereof |
JOP20200024A1 (ar) | 2017-08-04 | 2020-02-02 | Bayer Ag | مركبات ثنائي هيدروكساديازينون |
US11897867B2 (en) | 2017-08-04 | 2024-02-13 | Bayer Aktiengesellschaft | 6-phenyl-4,5-dihydropyridazin-3(2H)-one derivatives as PDE3A and PDE3B inhibitors for treating cancer |
CN107821390A (zh) * | 2017-10-13 | 2018-03-23 | 南京扬子鸿利源化学品有限责任公司 | 一种甲基磺草酮油悬浮剂及其制备方法 |
EP3712150A4 (en) | 2017-11-01 | 2021-03-10 | Shijiazhuang Sagacity New Drug Development Co., Ltd. | MACROCYCLIC COMPOUND SERVING AS AN INHIBITOR OF WEE1 AND ITS APPLICATIONS |
MA52493A (fr) | 2018-05-04 | 2021-03-10 | Incyte Corp | Sels d'un inhibiteur de fgfr |
SG11202010636VA (en) | 2018-05-04 | 2020-11-27 | Incyte Corp | Solid forms of an fgfr inhibitor and processes for preparing the same |
CN108727249A (zh) * | 2018-07-07 | 2018-11-02 | 台州学院 | 3-二氟甲基哌啶盐酸盐及其衍生物的合成方法 |
KR20210066839A (ko) * | 2018-09-27 | 2021-06-07 | 베타 파머수티컬 컴퍼니 리미티드 | Fgfr4 저해제 및 그것의 용도 |
US11066404B2 (en) | 2018-10-11 | 2021-07-20 | Incyte Corporation | Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors |
WO2020083404A1 (zh) | 2018-10-26 | 2020-04-30 | 南京明德新药研发有限公司 | 作为Wee1抑制剂的嘧啶并吡唑酮类衍生物及其应用 |
US11384083B2 (en) | 2019-02-15 | 2022-07-12 | Incyte Corporation | Substituted spiro[cyclopropane-1,5′-pyrrolo[2,3-d]pyrimidin]-6′(7′h)-ones as CDK2 inhibitors |
TW202100520A (zh) | 2019-03-05 | 2021-01-01 | 美商英塞特公司 | 作為cdk2 抑制劑之吡唑基嘧啶基胺化合物 |
US11628162B2 (en) | 2019-03-08 | 2023-04-18 | Incyte Corporation | Methods of treating cancer with an FGFR inhibitor |
US11919904B2 (en) | 2019-03-29 | 2024-03-05 | Incyte Corporation | Sulfonylamide compounds as CDK2 inhibitors |
CN113784968B (zh) | 2019-04-30 | 2024-03-15 | 无锡智康弘义生物科技有限公司 | Wee1抑制剂化合物的晶型及其应用 |
US11440914B2 (en) | 2019-05-01 | 2022-09-13 | Incyte Corporation | Tricyclic amine compounds as CDK2 inhibitors |
US11447494B2 (en) | 2019-05-01 | 2022-09-20 | Incyte Corporation | Tricyclic amine compounds as CDK2 inhibitors |
WO2021007269A1 (en) | 2019-07-09 | 2021-01-14 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
JP2023509260A (ja) | 2019-08-14 | 2023-03-08 | インサイト・コーポレイション | Cdk2阻害剤としてのイミダゾリルピリミジニルアミン化合物 |
CN112442049A (zh) * | 2019-09-03 | 2021-03-05 | 微境生物医药科技(上海)有限公司 | 作为Wee1抑制剂的嘧啶衍生物 |
WO2021072232A1 (en) | 2019-10-11 | 2021-04-15 | Incyte Corporation | Bicyclic amines as cdk2 inhibitors |
PE20221085A1 (es) | 2019-10-14 | 2022-07-05 | Incyte Corp | Heterociclos biciclicos como inhibidores de fgfr |
CN114502559B (zh) * | 2019-10-16 | 2024-02-02 | 上海瑛派药业有限公司 | 二氢咪唑并嘧啶并嘧啶酮类化合物 |
WO2021076728A1 (en) | 2019-10-16 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
CN115151539A (zh) | 2019-12-04 | 2022-10-04 | 因赛特公司 | Fgfr抑制剂的衍生物 |
WO2021113479A1 (en) | 2019-12-04 | 2021-06-10 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
AU2021290701A1 (en) | 2020-06-17 | 2023-02-02 | Wigen Biomedicine Technology (shanghai) Co., Ltd. | Pyrazolo(3,4-d)pyrimidine-3-ketone derivative as Wee-1 inhibitor |
WO2022174765A1 (zh) * | 2021-02-19 | 2022-08-25 | 微境生物医药科技(上海)有限公司 | 作为Wee-1抑制剂的稠环化合物 |
EP4332104A1 (en) * | 2021-04-30 | 2024-03-06 | Wigen Biomedicine Technology (Shanghai) Co., Ltd. | Fused ring compound as wee-1 inhibitor, and preparation method therefor and use thereof |
CA3220274A1 (en) | 2021-06-09 | 2022-12-15 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
WO2023083194A1 (zh) * | 2021-11-09 | 2023-05-19 | 杭州格博生物医药有限公司 | Wee1蛋白激酶降解剂及其用途 |
CN116836184A (zh) * | 2022-03-25 | 2023-10-03 | 药雅科技(上海)有限公司 | Wee1激酶抑制剂的制备及其应用 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE602004029293D1 (de) | 2003-07-25 | 2010-11-04 | Novartis Ag | p-38-Kinasehemmer |
US20050070554A1 (en) * | 2003-08-27 | 2005-03-31 | Amgen Inc. | Substituted heterocyclic compounds and methods of use |
US20050250836A1 (en) * | 2004-05-03 | 2005-11-10 | Pfizer Inc | Inhibitors of checkpoint kinases (Wee1 and Chk1) |
AR058277A1 (es) | 2005-12-09 | 2008-01-30 | Solvay Pharm Gmbh | N- sulfamoil - piperidin - amidas, composiciones farmaceuticas que las comprenden y procedimiento para su preparacion |
US8299080B2 (en) * | 2006-12-13 | 2012-10-30 | Aska Pharmaceutical Co., Ltd. | Substituted imidazo[1,5-A] quinoxalines as a PDE9 inhibitor |
CA2703489A1 (en) * | 2007-10-23 | 2009-04-30 | Banyu Pharmaceutical Co., Ltd. | Pyridone-substituted-dihydropyrazolopyrimidinone derivative |
WO2009151997A1 (en) | 2008-06-12 | 2009-12-17 | Merck & Co., Inc. | Process for producing bicycloaniline derivatives |
CA2745970A1 (en) * | 2008-12-12 | 2010-06-17 | Msd K.K. | Dihydropyrimidopyrimidine derivative |
-
2012
- 2012-02-24 TW TW101106325A patent/TWI532742B/zh not_active IP Right Cessation
- 2012-02-27 JP JP2013556755A patent/JP5886326B2/ja not_active Expired - Fee Related
- 2012-02-27 CN CN201280018862.6A patent/CN103703005A/zh active Pending
- 2012-02-27 WO PCT/US2012/026685 patent/WO2012161812A1/en active Application Filing
- 2012-02-27 CA CA2827648A patent/CA2827648A1/en not_active Abandoned
- 2012-02-27 UY UY0001033925A patent/UY33925A/es not_active Application Discontinuation
- 2012-02-27 ES ES12716781.5T patent/ES2587514T3/es active Active
- 2012-02-27 MX MX2013009873A patent/MX340402B/es active IP Right Grant
- 2012-02-27 EP EP12716781.5A patent/EP2681221B1/en not_active Not-in-force
- 2012-02-28 AR ARP120100641A patent/AR085502A1/es unknown
- 2012-02-28 US US13/406,937 patent/US8710065B2/en active Active
Also Published As
Publication number | Publication date |
---|---|
CN103703005A (zh) | 2014-04-02 |
TWI532742B (zh) | 2016-05-11 |
EP2681221B1 (en) | 2016-05-18 |
AR085502A1 (es) | 2013-10-09 |
US8710065B2 (en) | 2014-04-29 |
ES2587514T3 (es) | 2016-10-25 |
US20120220572A1 (en) | 2012-08-30 |
JP5886326B2 (ja) | 2016-03-16 |
TW201247675A (en) | 2012-12-01 |
EP2681221A1 (en) | 2014-01-08 |
UY33925A (es) | 2012-09-28 |
MX2013009873A (es) | 2014-03-12 |
CA2827648A1 (en) | 2012-11-29 |
JP2014506929A (ja) | 2014-03-20 |
WO2012161812A1 (en) | 2012-11-29 |
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Legal Events
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FG | Grant or registration |