MA38183A1 - Composés pyrrolopyrimidines en tant qu'inhibiteurs de kinase - Google Patents
Composés pyrrolopyrimidines en tant qu'inhibiteurs de kinaseInfo
- Publication number
- MA38183A1 MA38183A1 MA38183A MA38183A MA38183A1 MA 38183 A1 MA38183 A1 MA 38183A1 MA 38183 A MA38183 A MA 38183A MA 38183 A MA38183 A MA 38183A MA 38183 A1 MA38183 A1 MA 38183A1
- Authority
- MA
- Morocco
- Prior art keywords
- relates
- btk
- compounds
- inhibitors
- kinase inhibitors
- Prior art date
Links
Classifications
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- 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
- C07D487/02—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
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- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- 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 présente invention concerne des composés qui forment des liaisons covalentes avec la tyrosine kinase de bruton (btk). L'invention concerne également des inhibiteurs irréversibles de btk. De plus, l'invention concerne également des inhibiteurs réversibles de btk. L'invention concerne également des compositions pharmaceutiques qui comprennent les composés. L'invention concerne des procédés d'utilisation des inhibiteurs de btk, seuls en combinaison avec d'autres agents thérapeutiques, pour le traitement de maladies auto-immunes ou d'états auto-immuns, de maladies hétéro-immunes ou d'états hétéro-immuns, le cancer, comprenant un lymphome, et des maladies ou états inflammatoires.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201261727031P | 2012-11-15 | 2012-11-15 | |
PCT/US2013/070164 WO2014078578A1 (fr) | 2012-11-15 | 2013-11-14 | Composés pyrrolopyrimidines en tant qu'inhibiteurs de kinase |
Publications (1)
Publication Number | Publication Date |
---|---|
MA38183A1 true MA38183A1 (fr) | 2017-03-31 |
Family
ID=50728514
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA38183A MA38183A1 (fr) | 2012-11-15 | 2013-11-14 | Composés pyrrolopyrimidines en tant qu'inhibiteurs de kinase |
Country Status (24)
Country | Link |
---|---|
US (3) | US9096604B2 (fr) |
EP (1) | EP2920180A4 (fr) |
JP (1) | JP2015537033A (fr) |
KR (1) | KR20150084923A (fr) |
CN (1) | CN104854107A (fr) |
AR (1) | AR093518A1 (fr) |
AU (1) | AU2013344656A1 (fr) |
BR (1) | BR112015011171A2 (fr) |
CA (1) | CA2890934A1 (fr) |
CL (1) | CL2015001268A1 (fr) |
CR (1) | CR20150263A (fr) |
DO (1) | DOP2015000108A (fr) |
EA (1) | EA201590855A1 (fr) |
HK (1) | HK1215253A1 (fr) |
IL (1) | IL238728A0 (fr) |
MA (1) | MA38183A1 (fr) |
MX (1) | MX2015006168A (fr) |
NI (1) | NI201500067A (fr) |
PE (1) | PE20151495A1 (fr) |
PH (1) | PH12015501067A1 (fr) |
SG (1) | SG11201503842PA (fr) |
TN (1) | TN2015000174A1 (fr) |
TW (1) | TWI522359B (fr) |
WO (1) | WO2014078578A1 (fr) |
Families Citing this family (49)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20120101114A1 (en) | 2007-03-28 | 2012-04-26 | Pharmacyclics, Inc. | Inhibitors of bruton's tyrosine kinase |
WO2010009342A2 (fr) | 2008-07-16 | 2010-01-21 | Pharmacyclics, Inc. | Inhibiteurs de tyrosine kinase de bruton pour le traitement de tumeurs solides |
CA2800913C (fr) | 2010-06-03 | 2019-07-23 | Pharmacyclics, Inc. | Utilisation d'inhibiteurs de la tyrosine kinase de bruton (btk) |
PL2710005T3 (pl) | 2011-05-17 | 2017-07-31 | Principia Biopharma Inc. | Inhibitory kinazy tyrozynowej |
US9376438B2 (en) | 2011-05-17 | 2016-06-28 | Principia Biopharma, Inc. | Pyrazolopyrimidine derivatives as tyrosine kinase inhibitors |
WO2013010136A2 (fr) | 2011-07-13 | 2013-01-17 | Pharmacyclics, Inc. | Inhibiteurs de tyrosine kinase de bruton |
US9416132B2 (en) | 2011-07-21 | 2016-08-16 | Tolero Pharmaceuticals, Inc. | Substituted imidazo[1,2-b]pyridazines as protein kinase inhibitors |
US8377946B1 (en) | 2011-12-30 | 2013-02-19 | Pharmacyclics, Inc. | Pyrazolo[3,4-d]pyrimidine and pyrrolo[2,3-d]pyrimidine compounds as kinase inhibitors |
CN110354132A (zh) | 2012-06-04 | 2019-10-22 | 药品循环有限责任公司 | 布鲁顿酪氨酸激酶抑制剂的晶形 |
EP2877598A1 (fr) | 2012-07-24 | 2015-06-03 | Pharmacyclics, Inc. | Mutations associées à la résistance à des inhibiteurs de la tyrosine kinase de bruton (btk) |
SI2892900T1 (en) | 2012-09-10 | 2018-01-31 | Principia Biopharma Inc. | Compounds of pyrazolopyrimidine, as kinase inhibitors |
BR112015011171A2 (pt) * | 2012-11-15 | 2017-07-11 | Pharmacyclics Inc | compostos de pirrolopirimidina como inibidores da quinase |
CN108997225A (zh) | 2013-03-14 | 2018-12-14 | 特雷罗药物股份有限公司 | Jak2和alk2抑制剂及其使用方法 |
US8957080B2 (en) | 2013-04-09 | 2015-02-17 | Principia Biopharma Inc. | Tyrosine kinase inhibitors |
ES2709509T3 (es) | 2013-08-12 | 2019-04-16 | Pharmacyclics Llc | Procedimientos para el tratamiento de cáncer amplificado por HER2 |
MX2016004030A (es) * | 2013-09-30 | 2016-10-26 | Beijing Synercare Pharma Tech Co Ltd | Inhibidores sustituidos de nicotinamida de btk y su preparacion y uso en el tratamiento del cancer, inflamacion y enfermedad autoinmune. |
KR20160062103A (ko) | 2013-09-30 | 2016-06-01 | 파마싸이클릭스 엘엘씨 | 브루톤 티로신 키나제의 억제제 |
CA2939186C (fr) | 2014-02-21 | 2023-03-07 | Principia Biopharma Inc. | Sels et forme solide d'un inhibiteur de btk |
WO2015143400A1 (fr) | 2014-03-20 | 2015-09-24 | Pharmacyclics, Inc. | Mutations de phospholipase c gamma 2 et associées aux résistances |
US9533991B2 (en) | 2014-08-01 | 2017-01-03 | Pharmacyclics Llc | Inhibitors of Bruton's tyrosine kinase |
SG11201700849XA (en) | 2014-08-07 | 2017-03-30 | Pharmacyclics Llc | Novel formulations of a bruton's tyrosine kinase inhibitor |
WO2016100914A1 (fr) | 2014-12-18 | 2016-06-23 | Gourlay Steven | Traitement du pemphigus |
AU2016226279B2 (en) | 2015-03-03 | 2021-11-11 | Pharmacyclics Llc | Pharmaceutical formulations of Bruton's tyrosine kinase inhibtor |
TW201718572A (zh) | 2015-06-24 | 2017-06-01 | 普林斯匹亞生物製藥公司 | 酪胺酸激酶抑制劑 |
US10550124B2 (en) * | 2015-08-13 | 2020-02-04 | San Diego State University Foundation | Atropisomerism for increased kinase inhibitor selectivity |
CN108431007B (zh) * | 2015-09-16 | 2022-06-07 | 洛克索肿瘤学股份有限公司 | 用于治疗癌症的作为btk抑制剂的吡唑并嘧啶衍生物 |
WO2017106771A1 (fr) * | 2015-12-16 | 2017-06-22 | Southern Research Institute | Composés de pyrrolopyrimidine, leur utilisation à titre d'inhibiteurs de la kinase lrrk2, et leurs procédés de préparation |
CN107513068A (zh) * | 2016-06-16 | 2017-12-26 | 中国科学院上海药物研究所 | 一种具有fgfr抑制活性的新型化合物及其制备和应用 |
CA3028169A1 (fr) | 2016-06-29 | 2018-01-04 | Principia Biopharma Inc. | Formulations a liberation modifiee a base de 2-[3-[4-amino-3-(2-fluoro-4-phenoxy-phenyl)pyrazolo[3,4-d]pyrimidine-1-yl]piperidine-1-carbonyl]-4-methyl-4-[4-(oxetane-3-yl)piperazin e-1-yl]pent-2-enenitrile |
TWI757340B (zh) * | 2016-09-16 | 2022-03-11 | 美商生命醫藥有限責任公司 | 梅嫩蛋白(menin)-MLL相互作用之抑制劑 |
CN110545826A (zh) | 2016-12-03 | 2019-12-06 | 朱诺治疗学股份有限公司 | 用于与激酶抑制剂组合使用治疗性t细胞的方法和组合物 |
CN106588937B (zh) | 2017-01-16 | 2018-09-21 | 东莞市真兴贝特医药技术有限公司 | 咪唑并吡嗪类化合物及其制备方法和应用 |
CN106946896B (zh) * | 2017-03-30 | 2019-05-21 | 成都知普莱生物医药科技有限公司 | 呋喃并[2,3-d]嘧啶-4-胺衍生物 |
IT201700099690A1 (it) * | 2017-09-06 | 2019-03-06 | Abiogen Pharma Spa | Composizione per l’integrazione di calcio |
US11013741B1 (en) | 2018-04-05 | 2021-05-25 | Sumitomo Dainippon Pharma Oncology, Inc. | AXL kinase inhibitors and use of the same |
CN117838695A (zh) | 2018-04-13 | 2024-04-09 | 住友制药肿瘤公司 | 用于治疗骨髓增殖性肿瘤和与癌症相关的纤维化的pim激酶抑制剂 |
WO2020023910A1 (fr) | 2018-07-26 | 2020-01-30 | Tolero Pharmaceuticals, Inc. | Procédés de traitement de maladies associées à l'expression anormale d'acvr1 et inhibiteurs d'acvr1 destinés à être utilisés dans ceux-ci |
CN113412262A (zh) | 2019-02-12 | 2021-09-17 | 大日本住友制药肿瘤公司 | 包含杂环蛋白激酶抑制剂的制剂 |
CA3130049A1 (fr) * | 2019-02-15 | 2020-08-20 | Taiho Pharmaceutical Co., Ltd. | Derive de 7h-pyrrolo [2,3-d] pyrimidine-4-amine |
CN114364798A (zh) | 2019-03-21 | 2022-04-15 | 欧恩科斯欧公司 | 用于治疗癌症的Dbait分子与激酶抑制剂的组合 |
CN111825674A (zh) * | 2019-04-22 | 2020-10-27 | 上海仕谱生物科技有限公司 | 嘧啶并五元杂环类化合物及其作为突变型idh2抑制剂的用途 |
AU2020378630A1 (en) | 2019-11-08 | 2022-05-26 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for the treatment of cancers that have acquired resistance to kinase inhibitors |
WO2021148581A1 (fr) | 2020-01-22 | 2021-07-29 | Onxeo | Nouvelle molécule dbait et son utilisation |
CN113493439B (zh) * | 2020-03-20 | 2022-10-14 | 深圳市塔吉瑞生物医药有限公司 | 取代的丙烯酰胺衍生物及其组合物及用途 |
CN113527300B (zh) * | 2020-06-04 | 2023-02-03 | 广州百霆医药科技有限公司 | 布鲁顿酪氨酸蛋白激酶抑制剂 |
EP4247816A1 (fr) * | 2020-11-17 | 2023-09-27 | Relay Therapeutics, Inc. | Inhibiteurs de src et leurs utilisations |
WO2022140246A1 (fr) | 2020-12-21 | 2022-06-30 | Hangzhou Jijing Pharmaceutical Technology Limited | Procédés et composés destinés à l'autophagie ciblée |
WO2023078413A1 (fr) * | 2021-11-04 | 2023-05-11 | 微境生物医药科技(上海)有限公司 | Inhibiteur du fgfr2, son procédé de préparation et son utilisation pharmaceutique |
US20230277424A1 (en) * | 2022-03-03 | 2023-09-07 | Profounda Health And Beauty Inc. | Treatment composition for nasal and oral dryness, nosebleeds, and allergy symptoms |
Family Cites Families (98)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5052558A (en) | 1987-12-23 | 1991-10-01 | Entravision, Inc. | Packaged pharmaceutical product |
US5033252A (en) | 1987-12-23 | 1991-07-23 | Entravision, Inc. | Method of packaging and sterilizing a pharmaceutical product |
JPH01167840A (ja) | 1987-12-24 | 1989-07-03 | Konica Corp | 新規な写真用シアンカプラー |
US5323907A (en) | 1992-06-23 | 1994-06-28 | Multi-Comp, Inc. | Child resistant package assembly for dispensing pharmaceutical medications |
GB9226855D0 (en) | 1992-12-23 | 1993-02-17 | Erba Carlo Spa | Vinylene-azaindole derivatives and process for their preparation |
US6326469B1 (en) | 1994-04-22 | 2001-12-04 | Sugen, Inc. | Megakaryocytic protein tyrosine kinases |
US5593997A (en) | 1995-05-23 | 1997-01-14 | Pfizer Inc. | 4-aminopyrazolo(3-,4-D)pyrimidine and 4-aminopyrazolo-(3,4-D)pyridine tyrosine kinase inhibitors |
CH690773A5 (de) | 1996-02-01 | 2001-01-15 | Novartis Ag | Pyrrolo(2,3-d)pyrimide und ihre Verwendung. |
WO1997049706A1 (fr) | 1996-06-25 | 1997-12-31 | Novartis Ag | 7-AMINO-PYRROLO[3,2-d]PYRIMIDINES SUBSTITUES ET UTILISATION DE CES COMPOSES |
HUP0001507A3 (en) | 1997-03-19 | 2002-01-28 | Abbott Gmbh & Co Kg | Pyrrolo [2,3-d] pyrimidine derivatives, process for their preparation, their use and pharmaceutical compositions containing them |
IL139080A0 (en) | 1998-04-17 | 2001-11-25 | Parker Hughes Inst | Btx inhibitors and methods for their indentification and use |
US6303652B1 (en) | 1998-08-21 | 2001-10-16 | Hughes Institute | BTK inhibitors and methods for their identification and use |
US6335155B1 (en) | 1998-06-26 | 2002-01-01 | Sunesis Pharmaceuticals, Inc. | Methods for rapidly identifying small organic molecule ligands for binding to biological target molecules |
US20050287596A9 (en) | 1998-06-26 | 2005-12-29 | Braisted Andrew C | Novel ligands and libraries of ligands |
US6998233B2 (en) | 1998-06-26 | 2006-02-14 | Sunesis Pharmaceuticals, Inc. | Methods for ligand discovery |
US6306897B1 (en) | 1999-03-19 | 2001-10-23 | Parker Hughes Institute | Calanolides for inhibiting BTK |
PT1212327E (pt) | 1999-09-17 | 2004-01-30 | Abbott Gmbh & Co Kg | Pirazolopirimidinas como agentes terapeuticos |
US6921763B2 (en) | 1999-09-17 | 2005-07-26 | Abbott Laboratories | Pyrazolopyrimidines as therapeutic agents |
JP5036112B2 (ja) | 1999-10-06 | 2012-09-26 | ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド | チロシンキナーゼのインヒビターとして有益な複素環化合物 |
US6506769B2 (en) | 1999-10-06 | 2003-01-14 | Boehringer Ingelheim Pharmaceuticals, Inc. | Heterocyclic compounds useful as inhibitors of tyrosine kinases |
WO2001041754A2 (fr) | 1999-11-30 | 2001-06-14 | Parker Hughes Institute | Inhibiteurs d'agregation plaquettaire induite par le collagene |
AU2439701A (en) | 1999-12-17 | 2001-06-25 | Ariad Pharmaceuticals, Inc. | Novel heterocycles |
GB0005345D0 (en) | 2000-03-06 | 2000-04-26 | Mathilda & Terence Kennedy Ins | Methods of treating sepsis septic shock and inflammation |
WO2002038797A2 (fr) | 2000-10-23 | 2002-05-16 | Bristol-Myers Squibb Company | Modulateurs de tyrosine kinase de bruton et intermediaires de tyrosine kinase de bruton et leurs procedes d'identification et d'utilisation dans le traitement et la prevention de l'osteoporose et d'etats pathologiques connexes |
WO2002045684A2 (fr) | 2000-12-06 | 2002-06-13 | Pharmacia Corporation | Composition pharmaceutique a dispersion rapide |
MXPA03008560A (es) | 2001-03-22 | 2004-06-30 | Abbot Gmbh & Co Kg | Pirazolopirimidinas como agentes terapeuticos. |
US8306897B2 (en) | 2001-05-04 | 2012-11-06 | Stockshield, Inc. | Method and system for insuring against investment loss |
WO2003000187A2 (fr) | 2001-06-21 | 2003-01-03 | Ariad Pharmaceuticals, Inc. | Nouvelles pyrazolo-pyrimidines et pyrrolo-pyrimidines et leur utilisation |
CN1523991A (zh) | 2001-08-10 | 2004-08-25 | ��˹��ŵ�� | 单独的c-Src抑制剂或其与STI571的组合用于治疗白血病的用途 |
WO2003016338A1 (fr) | 2001-08-15 | 2003-02-27 | Parker Hughes Institute | Structure cristalline du domaine kinase de btk |
MXPA04004814A (es) | 2001-11-21 | 2004-08-11 | Sunesis Pharmaceuticals Inc | Metodos para descubrir ligandos. |
US20050084905A1 (en) | 2002-03-21 | 2005-04-21 | Prescott John C. | Identification of kinase inhibitors |
GB2388594A (en) | 2002-05-16 | 2003-11-19 | Bayer Ag | Imidazo-triazine PDE 4 inhibitors |
AU2003257094A1 (en) | 2002-08-08 | 2004-02-25 | Boehringer Ingelheim Pharmaceuticals, Inc. | Substituted benzimidazole compounds |
GB0303910D0 (en) | 2003-02-20 | 2003-03-26 | Merck Sharp & Dohme | Therapeutic agents |
WO2005000197A2 (fr) | 2003-04-11 | 2005-01-06 | The Regents Of The University Of California | Inhibiteurs selectifs de la serine/threonine kinase |
WO2004100868A2 (fr) | 2003-04-23 | 2004-11-25 | Abbott Laboratories | Procede servant a traiter le rejet d'un transplant |
EP1473039A1 (fr) | 2003-05-02 | 2004-11-03 | Centre National De La Recherche Scientifique (Cnrs) | Utilisation d'inhibiteurs et d'oligonucleotitides antisense de BTK pour le traitement de la mastocytose proliferative |
US7405295B2 (en) | 2003-06-04 | 2008-07-29 | Cgi Pharmaceuticals, Inc. | Certain imidazo[1,2-a]pyrazin-8-ylamines and method of inhibition of Bruton's tyrosine kinase by such compounds |
US7393848B2 (en) | 2003-06-30 | 2008-07-01 | Cgi Pharmaceuticals, Inc. | Certain heterocyclic substituted imidazo[1,2-A]pyrazin-8-ylamines and methods of inhibition of Bruton's tyrosine kinase by such compounds |
US8131475B2 (en) | 2003-09-03 | 2012-03-06 | The United States Of America As Represented By The Secretary, Department Of Health And Human Services | Methods for identifying, diagnosing, and predicting survival of lymphomas |
CN1897950A (zh) | 2003-10-14 | 2007-01-17 | 惠氏公司 | 稠合芳基和杂芳基衍生物及其使用方法 |
AU2004282219C1 (en) | 2003-10-15 | 2009-12-17 | Osi Pharmaceuticals, Inc. | Imidazo [1, 5 - a] pyrazine tyrosine kinase inhibitors |
AU2003297904A1 (en) | 2003-12-12 | 2005-07-14 | University Of Maryland, Baltimore | Immunomodulatory compounds that target and inhibit the py+3 binding site of tyrosene kinase p56 lck sh2 domain |
BRPI0418031A (pt) | 2003-12-22 | 2007-04-17 | Gilead Sciences Inc | inibidores de quinase fosfonato-substituìdos |
JP2007519742A (ja) | 2004-01-26 | 2007-07-19 | 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 | プロテインキナーゼの阻害剤として有用な組成物 |
US20060025383A1 (en) | 2004-02-03 | 2006-02-02 | Neil Wishart | Aminobenzoxazoles as therapeutic agents |
AR053090A1 (es) | 2004-07-20 | 2007-04-25 | Osi Pharm Inc | Imidazotriazinas como inhibidores de proteina quinasas y su uso para la preparacion de medicamentos |
JP2008514635A (ja) | 2004-09-27 | 2008-05-08 | コーザン バイオサイエンシス インコーポレイテッド | 特異的キナーゼ阻害剤 |
CA2582225A1 (fr) | 2004-09-28 | 2006-04-06 | Mingde Xia | Antagonistes anti-ccr2 a base de dipiperidine substituee |
MX2007005643A (es) | 2004-11-10 | 2008-03-13 | Cgi Pharmaceuticals Inc | Ciertas imidazo [1,2-a] pirazin-8-ilaminas, metodo para su elaboracion y metodo de uso de las mismas. |
GB0425035D0 (en) | 2004-11-12 | 2004-12-15 | Novartis Ag | Organic compounds |
WO2006099075A2 (fr) | 2005-03-10 | 2006-09-21 | Cgi Pharmaceuticals, Inc. | Amides substitues, procede pour les produire et procede pour les utiliser |
MX2007014066A (es) | 2005-05-13 | 2008-02-11 | Irm Llc | Compuestos y composiciones como inhibidores de cinasa de proteina. |
DK1893612T3 (da) | 2005-06-22 | 2011-11-21 | Plexxikon Inc | Pyrrol [2,3-B]pyridin-derivater som proteinkinasehæmmere |
US20070065449A1 (en) | 2005-09-16 | 2007-03-22 | Claire Verschraegen | Method of treating cancer, especially soft tissue sarcoma utilizing gemcitabine in combination with docetaxel and anti-VEGF therapy (bevacizumab) |
WO2007058832A2 (fr) | 2005-11-12 | 2007-05-24 | Boehringer Ingelheim International Gmbh | INHIBITEURS DES KINASES Tec |
AU2006336506B2 (en) | 2006-01-13 | 2012-06-28 | Pharmacyclics Llc | Inhibitors of tyrosine kinases and uses thereof |
JP2009525468A (ja) | 2006-01-30 | 2009-07-09 | ザ・スクリプス・リサーチ・インステイチユート | 循環腫瘍細胞の検出方法および哺乳類対象における癌の診断方法 |
MX2008012928A (es) | 2006-04-04 | 2009-03-06 | Univ California | Antagonistas de pi3-cinasa. |
EP2027087A2 (fr) | 2006-05-18 | 2009-02-25 | MannKind Corporation | Inhibiteurs de kinases intracellulaires |
HUE028086T2 (en) | 2006-09-22 | 2016-11-28 | Pharmacyclics Llc | Bruton tyrosine kinase inhibitors |
US8987233B2 (en) | 2006-11-03 | 2015-03-24 | Pharmacyclics, Inc. | Bruton's tyrosine kinase activity probe and method of using |
NL2000640C2 (nl) | 2007-03-05 | 2008-09-08 | Stichting Wetsus Ct Of Excelle | Werkwijze en systeem voor het zuiveren van een vloeistof. |
US20120101114A1 (en) | 2007-03-28 | 2012-04-26 | Pharmacyclics, Inc. | Inhibitors of bruton's tyrosine kinase |
CA3001152A1 (fr) | 2007-03-28 | 2008-10-09 | Pharmacyclics Llc | Inhibiteurs de la tyrosine kinase de bruton |
US20120065201A1 (en) | 2007-03-28 | 2012-03-15 | Pharmacyclics, Inc. | Inhibitors of bruton's tyrosine kinase |
US20090010911A1 (en) | 2007-04-06 | 2009-01-08 | Iowa State University Research Foundation, Inc. | Methods and compositions for affecting cyclophilin a regulation of kinases in modulating cellular activities |
TWI552752B (zh) | 2007-10-19 | 2016-10-11 | 賽基艾維洛米斯研究股份有限公司 | 雜芳基化合物及其用途 |
US7989465B2 (en) | 2007-10-19 | 2011-08-02 | Avila Therapeutics, Inc. | 4,6-disubstituted pyrimidines useful as kinase inhibitors |
SG185330A1 (en) | 2007-10-23 | 2012-11-29 | Hoffmann La Roche | Novel kinase inhibitors |
US8426441B2 (en) | 2007-12-14 | 2013-04-23 | Roche Palo Alto Llc | Inhibitors of bruton's tyrosine kinase |
US20150152115A1 (en) | 2007-12-27 | 2015-06-04 | Pharmacyclics, Inc. | Inhibitors of bruton's tyrosine kinase |
RU2536584C2 (ru) | 2008-06-27 | 2014-12-27 | Авила Терапьютикс, Инк. | Гетероарильные соединения и их применение |
WO2010009342A2 (fr) | 2008-07-16 | 2010-01-21 | Pharmacyclics, Inc. | Inhibiteurs de tyrosine kinase de bruton pour le traitement de tumeurs solides |
US20100185419A1 (en) | 2008-09-05 | 2010-07-22 | Avila Therapeutics, Inc. | Algorithm for designing irreversible inhibitors |
US8426428B2 (en) * | 2008-12-05 | 2013-04-23 | Principia Biopharma, Inc. | EGFR kinase knockdown via electrophilically enhanced inhibitors |
JP5656976B2 (ja) | 2009-04-29 | 2015-01-21 | ローカス ファーマシューティカルズ インコーポレイテッド | ピロロトリアジン化合物 |
US9556426B2 (en) | 2009-09-16 | 2017-01-31 | Celgene Avilomics Research, Inc. | Protein kinase conjugates and inhibitors |
US7718662B1 (en) | 2009-10-12 | 2010-05-18 | Pharmacyclics, Inc. | Pyrazolo-pyrimidine inhibitors of bruton's tyrosine kinase |
CN102918040B (zh) | 2010-05-31 | 2015-03-18 | 小野药品工业株式会社 | 6-羟基嘌呤衍生物 |
US20120071497A1 (en) | 2010-06-03 | 2012-03-22 | Pharmacyclics, Inc. | Methods of treating abc-dlbcl using inhibitors of bruton's tyrosine kinase |
CA2800913C (fr) | 2010-06-03 | 2019-07-23 | Pharmacyclics, Inc. | Utilisation d'inhibiteurs de la tyrosine kinase de bruton (btk) |
UA108889C2 (uk) | 2010-06-23 | 2015-06-25 | Конденсовані піримідинові похідні для інгібування тирозинкіназної активності | |
SG187796A1 (en) | 2010-08-10 | 2013-03-28 | Celgene Avilomics Res Inc | Besylate salt of a btk inhibitor |
PL2710005T3 (pl) * | 2011-05-17 | 2017-07-31 | Principia Biopharma Inc. | Inhibitory kinazy tyrozynowej |
US8377946B1 (en) | 2011-12-30 | 2013-02-19 | Pharmacyclics, Inc. | Pyrazolo[3,4-d]pyrimidine and pyrrolo[2,3-d]pyrimidine compounds as kinase inhibitors |
US8501724B1 (en) | 2012-01-31 | 2013-08-06 | Pharmacyclics, Inc. | Purinone compounds as kinase inhibitors |
CN110354132A (zh) | 2012-06-04 | 2019-10-22 | 药品循环有限责任公司 | 布鲁顿酪氨酸激酶抑制剂的晶形 |
DK2861599T3 (da) * | 2012-06-18 | 2020-03-02 | Principia Biopharma Inc | Reversible kovalente pyrrolo- eller pyrazolopyrimidiner, der er nyttige til behandling af cancer og autoimmunsygdomme |
EP2877598A1 (fr) | 2012-07-24 | 2015-06-03 | Pharmacyclics, Inc. | Mutations associées à la résistance à des inhibiteurs de la tyrosine kinase de bruton (btk) |
BR112015011171A2 (pt) | 2012-11-15 | 2017-07-11 | Pharmacyclics Inc | compostos de pirrolopirimidina como inibidores da quinase |
RU2705204C2 (ru) | 2013-05-30 | 2019-11-06 | Инфинити Фармасьютикалз, Инк. | Лечение злокачественных опухолей с использованием модуляторов изоформ piз-киназы |
CA2919996A1 (fr) | 2013-08-02 | 2015-02-05 | Pharmacyclics Llc | Methodes permettant de traiter des tumeurs solides |
JP6508785B2 (ja) | 2013-10-25 | 2019-05-08 | ファーマサイクリックス エルエルシー | ブルトンチロシンキナーゼ阻害剤および免疫療法を使用する処置 |
CN106008515A (zh) | 2014-01-29 | 2016-10-12 | 苏州晶云药物科技有限公司 | 依鲁替尼的新晶型及其制备方法 |
US20150238490A1 (en) | 2014-02-21 | 2015-08-27 | Pharmacyclics, Inc. | Biomarkers for predicting response of dlbcl to treatment with ibrutinib |
WO2015143400A1 (fr) | 2014-03-20 | 2015-09-24 | Pharmacyclics, Inc. | Mutations de phospholipase c gamma 2 et associées aux résistances |
-
2013
- 2013-11-14 BR BR112015011171A patent/BR112015011171A2/pt not_active IP Right Cessation
- 2013-11-14 JP JP2015542791A patent/JP2015537033A/ja active Pending
- 2013-11-14 AU AU2013344656A patent/AU2013344656A1/en not_active Abandoned
- 2013-11-14 PE PE2015000625A patent/PE20151495A1/es not_active Application Discontinuation
- 2013-11-14 CN CN201380059811.2A patent/CN104854107A/zh active Pending
- 2013-11-14 MA MA38183A patent/MA38183A1/fr unknown
- 2013-11-14 EP EP13854424.2A patent/EP2920180A4/fr not_active Withdrawn
- 2013-11-14 KR KR1020157015148A patent/KR20150084923A/ko not_active Application Discontinuation
- 2013-11-14 EA EA201590855A patent/EA201590855A1/ru unknown
- 2013-11-14 SG SG11201503842PA patent/SG11201503842PA/en unknown
- 2013-11-14 MX MX2015006168A patent/MX2015006168A/es unknown
- 2013-11-14 WO PCT/US2013/070164 patent/WO2014078578A1/fr active Application Filing
- 2013-11-14 CA CA2890934A patent/CA2890934A1/fr not_active Abandoned
- 2013-11-15 TW TW102141817A patent/TWI522359B/zh not_active IP Right Cessation
- 2013-11-15 US US14/081,053 patent/US9096604B2/en active Active
- 2013-11-18 AR ARP130104233A patent/AR093518A1/es unknown
-
2015
- 2015-05-06 TN TNP2015000174A patent/TN2015000174A1/fr unknown
- 2015-05-08 US US14/708,099 patent/US9540385B2/en active Active
- 2015-05-10 IL IL238728A patent/IL238728A0/en unknown
- 2015-05-12 CL CL2015001268A patent/CL2015001268A1/es unknown
- 2015-05-12 DO DO2015000108A patent/DOP2015000108A/es unknown
- 2015-05-14 NI NI201500067A patent/NI201500067A/es unknown
- 2015-05-14 PH PH12015501067A patent/PH12015501067A1/en unknown
- 2015-05-19 CR CR20150263A patent/CR20150263A/es unknown
-
2016
- 2016-03-18 HK HK16103201.1A patent/HK1215253A1/zh unknown
- 2016-09-09 US US15/261,414 patent/US20160375026A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
US20160375026A1 (en) | 2016-12-29 |
EP2920180A1 (fr) | 2015-09-23 |
SG11201503842PA (en) | 2015-06-29 |
BR112015011171A2 (pt) | 2017-07-11 |
EA201590855A1 (ru) | 2015-11-30 |
PE20151495A1 (es) | 2015-10-23 |
TN2015000174A1 (en) | 2016-10-03 |
CR20150263A (es) | 2015-08-24 |
US9540385B2 (en) | 2017-01-10 |
US20140142126A1 (en) | 2014-05-22 |
HK1215253A1 (zh) | 2016-08-19 |
CN104854107A (zh) | 2015-08-19 |
EP2920180A4 (fr) | 2016-04-13 |
CA2890934A1 (fr) | 2014-05-22 |
US20150239897A1 (en) | 2015-08-27 |
KR20150084923A (ko) | 2015-07-22 |
CL2015001268A1 (es) | 2015-07-10 |
WO2014078578A1 (fr) | 2014-05-22 |
IL238728A0 (en) | 2015-06-30 |
DOP2015000108A (es) | 2015-06-30 |
NI201500067A (es) | 2016-02-15 |
TW201425315A (zh) | 2014-07-01 |
JP2015537033A (ja) | 2015-12-24 |
TWI522359B (zh) | 2016-02-21 |
MX2015006168A (es) | 2015-08-10 |
PH12015501067A1 (en) | 2015-08-10 |
US9096604B2 (en) | 2015-08-04 |
AR093518A1 (es) | 2015-06-10 |
AU2013344656A1 (en) | 2015-06-04 |
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