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
-
- 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
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
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 (51)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20120101114A1 (en) | 2007-03-28 | 2012-04-26 | Pharmacyclics, Inc. | Inhibitors of bruton's tyrosine kinase |
CN102159214A (zh) | 2008-07-16 | 2011-08-17 | 药品循环公司 | 用于实体肿瘤的治疗的布鲁顿酪氨酸激酶的抑制剂 |
MY191929A (en) | 2010-06-03 | 2022-07-18 | Pharmacyclics Llc | The use of inhibitors of bruton's tyrosine kinase (btk) |
HUE033019T2 (en) | 2011-05-17 | 2017-11-28 | Principia Biopharma Inc | Tyrosine kinase inhibitors |
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 |
ES2671748T3 (es) | 2011-07-21 | 2018-06-08 | Tolero Pharmaceuticals, Inc. | Inhibidores heterocíclicos de proteína quinasas |
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 |
TWI662964B (zh) | 2012-06-04 | 2019-06-21 | 美商製藥有限責任公司 | 布魯頓氏酪胺酸激酶抑制劑之結晶形式 |
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) |
LT3181567T (lt) | 2012-09-10 | 2019-07-25 | Principia Biopharma Inc. | Pirazolpirimidino junginiai kaip kinazės slopikliai |
SG11201503842PA (en) | 2012-11-15 | 2015-06-29 | Pharmacyclics Inc | Pyrrolopyrimidine compounds as kinase inhibitors |
RU2019119893A (ru) | 2013-03-14 | 2019-08-09 | Толеро Фармасьютикалз, Инк. | Ингибиторы jak2 и alk2 и способы их использования |
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 |
KR102272792B1 (ko) | 2013-09-30 | 2021-07-05 | 광저우 이노케어 파마 테크 씨오., 엘티디. | Btk의 치환된 니코틴이미드 저해제 및 그의 제조 방법 및 암, 염증 및 자가면역 질환에의 용도 |
MA38961A1 (fr) | 2013-09-30 | 2018-05-31 | Pharmacyclics Llc | Composés 3-phenyl-1h-pyrazolo[3,4-d]pyrimidin-4-ylamine substitués inhibiteurs de la tyrosine kinase de bruton utilisés pour traiter par exemple les maladies auto-immunes, respiratoires et inflammatoires, cancer, mastocytose et osteoporose |
ES2841248T3 (es) | 2014-02-21 | 2021-07-07 | Principia Biopharma Inc | Sales y forma sólida de un inhibidor de BTK |
US9885086B2 (en) | 2014-03-20 | 2018-02-06 | Pharmacyclics Llc | Phospholipase C gamma 2 and resistance associated mutations |
CA2959602A1 (fr) * | 2014-08-01 | 2016-02-04 | Pharmacyclics Llc | Inhibiteurs de la tyrosine kinase de bruton |
MX2017001671A (es) | 2014-08-07 | 2017-07-04 | Pharmacyclics Llc | Formulaciones novedosas de un inhibidor de la tirosina cinasa de bruton. |
CA2970723C (fr) | 2014-12-18 | 2023-09-05 | Principia Biopharma Inc. | Traitement du pemphigus |
TWI810588B (zh) | 2015-03-03 | 2023-08-01 | 美商製藥公司 | 布魯東氏(bruton’s)酪胺酸激酶抑制劑之醫藥調配物 |
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 |
WO2017027883A1 (fr) * | 2015-08-13 | 2017-02-16 | San Diego State University Research Foundation | Atropisomérisme pour une sélectivité accrue des inhibiteurs de kinase |
AU2016322063A1 (en) * | 2015-09-16 | 2018-04-12 | Loxo Oncology, Inc. | Pyrazolopyrimidine derivatives as BTK inhibitors for the treatment of cancer |
CN108934162A (zh) * | 2015-12-16 | 2018-12-04 | 南方研究所 | 吡咯并嘧啶化合物、作为激酶lrrk2抑制剂的用途及其制备方法 |
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 |
EP3478273A1 (fr) | 2016-06-29 | 2019-05-08 | Principia Biopharma Inc. | Formulations à libération modifiée à base de 2-[3-[4-amino-3-(2-fluoro-4-phénoxy-phényl)pyrazolo[3,4-d]pyrimidine-1-yl]pipéridine-1-carbonyl]-4-méthyl-4-[4-(oxétane-3-yl)pipérazine-1-yl]pent-2-ènenitrile |
IL265028B (en) | 2016-09-16 | 2022-09-01 | Vitae Pharmaceuticals Llc | Inhibitors of the menin-mil interaction |
MX2019006288A (es) | 2016-12-03 | 2020-10-01 | Juno Therapeutics Inc | Metodos y composiciones para el uso de celulas t terapeuticas en combinacion con inhibidores de quinasa. |
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 |
EP3773560A4 (fr) | 2018-04-13 | 2022-01-19 | Sumitomo Dainippon Pharma Oncology, Inc. | Inhibiteurs de kinase pim pour le traitement de néoplasmes myéloprolifératifs et de fibrose associée au cancer |
AU2019310590A1 (en) | 2018-07-26 | 2021-01-14 | Sumitomo Pharma Oncology, Inc. | Methods for treating diseases associated with abnormal acvr1 expression and acvr1 inhibitors for use in the same |
AU2020221247A1 (en) | 2019-02-12 | 2021-08-05 | Sumitomo Pharma Oncology, Inc. | Formulations comprising heterocyclic protein kinase inhibitors |
BR112021015813A2 (pt) * | 2019-02-15 | 2021-10-13 | Taiho Pharmaceutical Co., Ltd. | Derivado de 7h-pirrolo[2,3-d]pirimidina-4-amina |
MX2021009863A (es) | 2019-03-21 | 2021-11-12 | Onxeo | Una molecula dbait en combinacion con inhibidor de quinasa para el tratamiento del cancer. |
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 |
KR20220098759A (ko) | 2019-11-08 | 2022-07-12 | 인쎄름 (엥스띠뛰 나씨오날 드 라 쌍떼 에 드 라 흐쉐르슈 메디깔) | 키나제 억제제에 대해 내성을 획득한 암의 치료 방법 |
CA3168146A1 (fr) | 2020-01-20 | 2021-07-29 | Genzyme Corporation | Inhibiteurs therapeutiques de la tyrosine kinase pour la sclerose en plaques recurrente (rms) |
WO2021148581A1 (fr) | 2020-01-22 | 2021-07-29 | Onxeo | Nouvelle molécule dbait et son utilisation |
WO2021185348A1 (fr) * | 2020-03-20 | 2021-09-23 | 深圳市塔吉瑞生物医药有限公司 | Dérivé d'acrylamide substitué et composition et utilisation associée |
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 |
US20240100172A1 (en) | 2020-12-21 | 2024-03-28 | Hangzhou Jijing Pharmaceutical Technology Limited | Methods and compounds for targeted autophagy |
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 |
US12016941B2 (en) * | 2022-03-03 | 2024-06-25 | Profounda Health And Beauty Inc. | Treatment composition for nasal and oral dryness, nosebleeds, and allergy symptoms |
WO2024097653A1 (fr) | 2022-10-31 | 2024-05-10 | Sumitomo Pharma America, Inc. | Inhibiteur de pim-1 pour le traitement de néoplasmes myéloprolifératifs |
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. |
AU3176297A (en) | 1996-06-25 | 1998-01-14 | Novartis Ag | Substituted 7-amino-pyrrolo{3,2-d}pyrimidines and the use thereof |
WO1998041525A1 (fr) | 1997-03-19 | 1998-09-24 | Basf Aktiengesellschaft | Pyrrolo [2,3] pyrimidines et leur utilisation comme inhibiteurs de la tyrosine kinase |
JP2002512216A (ja) | 1998-04-17 | 2002-04-23 | パーカー ヒューズ インスティテュート | Btkインヒビターならびにその同定方法および使用方法 |
US6303652B1 (en) | 1998-08-21 | 2001-10-16 | Hughes Institute | BTK inhibitors and methods for their identification and use |
US6998233B2 (en) | 1998-06-26 | 2006-02-14 | Sunesis Pharmaceuticals, Inc. | Methods for ligand discovery |
US20050287596A9 (en) | 1998-06-26 | 2005-12-29 | Braisted Andrew C | Novel ligands and libraries of ligands |
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 |
US6306897B1 (en) | 1999-03-19 | 2001-10-23 | Parker Hughes Institute | Calanolides for inhibiting BTK |
EP1212327B8 (fr) | 1999-09-17 | 2004-02-25 | Abbott GmbH & Co. KG | Pyrazolopyrimidines en tant qu'agents therapeutiques |
US6921763B2 (en) | 1999-09-17 | 2005-07-26 | Abbott Laboratories | Pyrazolopyrimidines as therapeutic agents |
EP1222187B1 (fr) | 1999-10-06 | 2004-09-22 | Boehringer Ingelheim Pharmaceuticals Inc. | Composes heterocycliques utiles comme inhibiteurs de tyrosine kinases |
US6506769B2 (en) | 1999-10-06 | 2003-01-14 | Boehringer Ingelheim Pharmaceuticals, Inc. | Heterocyclic compounds useful as inhibitors of tyrosine kinases |
AU4508601A (en) | 1999-11-30 | 2001-06-18 | Parker Hughes Institute | Inhibitors of collagen-induced platelet aggregation |
WO2001044258A1 (fr) | 1999-12-17 | 2001-06-21 | Ariad Pharmaceuticals, Inc. | Nouveaux heterocycles |
GB0005345D0 (en) | 2000-03-06 | 2000-04-26 | Mathilda & Terence Kennedy Ins | Methods of treating sepsis septic shock and inflammation |
US20030040461A1 (en) | 2000-10-23 | 2003-02-27 | Mcatee C. Patrick | Modulators of Bruton'sTyrosine Kinase and Bruton's Tyrosine Kinase intermediates and methods for their identification and use in the treatment and prevention of osteoporosis and related diseases states |
JP2004514732A (ja) | 2000-12-06 | 2004-05-20 | ファルマシア・コーポレーション | 迅速に分散する医薬組成物 |
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 |
AU2002315389A1 (en) | 2001-06-21 | 2003-01-08 | Ariad Pharmaceuticals, Inc. | Novel pyrazolo-and pyrrolo-pyrimidines and uses thereof |
EP2258371A1 (fr) | 2001-08-10 | 2010-12-08 | Novartis AG | Utilisation d'inhibiteurs c-Src seuls ou en combinaison avec STI571 pour le traitement de leucemies |
WO2003016338A1 (fr) | 2001-08-15 | 2003-02-27 | Parker Hughes Institute | Structure cristalline du domaine kinase de btk |
EP1446496A4 (fr) | 2001-11-21 | 2005-03-30 | Sunesis Pharmaceuticals Inc | Procedes de decouverte de ligands |
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 |
WO2004014905A1 (fr) | 2002-08-08 | 2004-02-19 | Boehringer Ingelheim Pharmaceuticals, Inc. | Composes benzimidazole substitues |
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 |
US20050008640A1 (en) | 2003-04-23 | 2005-01-13 | Wendy Waegell | Method of treating transplant rejection |
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 |
WO2005014599A1 (fr) | 2003-06-04 | 2005-02-17 | Cellular Genomics, Inc. | Imidazo[1,2-a]pyrazin-8-ylamines et methodes d'inhibition de la tyrosine kinase de bruton par de tels composes |
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 |
KR100872204B1 (ko) | 2003-10-15 | 2008-12-09 | 오에스아이 파마슈티컬스, 인코포레이티드 | 이미다조피라진 티로신 키나제 억제제 |
WO2005060956A1 (fr) | 2003-12-12 | 2005-07-07 | University Of Maryland, Baltimore | Composes immunomodulateurs de ciblage et d'inhibition du site de liaison py+3 du domaine sh2 de la proteine p56 tyrosine kinase |
BRPI0418031A (pt) | 2003-12-22 | 2007-04-17 | Gilead Sciences Inc | inibidores de quinase fosfonato-substituìdos |
EP1716151A1 (fr) | 2004-01-26 | 2006-11-02 | Vertex Pharmaceuticals Incorporated | Compositions utilisees en tant qu'inhibiteurs des proteines kinases |
CA2553724A1 (fr) | 2004-02-03 | 2005-08-18 | Abbott Laboratories | Utilisation d'aminobenzoxazoles comme agents therapeutiques |
MY139689A (en) | 2004-07-20 | 2009-10-30 | Osi Pharm Inc | Imidazotriazines as protein kinase inhibitors |
CA2581375A1 (fr) | 2004-09-27 | 2006-04-06 | Kosan Biosciences Incorporated | Inhibiteurs de kinases specifiques |
CA2582225A1 (fr) | 2004-09-28 | 2006-04-06 | Mingde Xia | Antagonistes anti-ccr2 a base de dipiperidine substituee |
CA2587192A1 (fr) | 2004-11-10 | 2006-05-18 | Cgi Pharmaceuticals, Inc. | Certaines imidazo[1,2-a] pyrazin-8-ylamines et les procedes de fabrication et d'utilisation correspondants |
GB0425035D0 (en) | 2004-11-12 | 2004-12-15 | Novartis Ag | Organic compounds |
JP2008533032A (ja) | 2005-03-10 | 2008-08-21 | シージーアイ ファーマシューティカルズ,インコーポレイティド | 或る種の置換アミド、その製造方法及び使用方法 |
AU2006247757B2 (en) | 2005-05-13 | 2009-08-27 | Irm, Llc | Compounds and compositions as protein kinase inhibitors |
MY153898A (en) | 2005-06-22 | 2015-04-15 | Plexxikon Inc | Compounds and methods for kinase modulation, and indications therefor |
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) |
EP1957491A2 (fr) | 2005-11-12 | 2008-08-20 | Boehringer Ingelheim International GmbH | Derives de pyrrolo (2,3-b) pyridine utiles comme inhibiteurs de tec kinase |
CA2636696A1 (fr) | 2006-01-13 | 2007-08-02 | Pharmacyclics, Inc. | Inhibiteurs de tyrosine kinase et leurs utilisations |
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. |
CA2651732C (fr) | 2006-05-18 | 2014-10-14 | Mannkind Corporation | Inhibiteurs de kinases intracellulaires |
EP2201840B1 (fr) | 2006-09-22 | 2011-11-02 | Pharmacyclics, Inc. | Inhibiteurs de la tyrosine kinase de Bruton |
EP2089391B1 (fr) | 2006-11-03 | 2013-01-16 | Pharmacyclics, Inc. | Sonde d'activité de la tyrosine kinase de bruton et son procédé d'utilisation |
NL2000640C2 (nl) | 2007-03-05 | 2008-09-08 | Stichting Wetsus Ct Of Excelle | Werkwijze en systeem voor het zuiveren van een vloeistof. |
US20120065201A1 (en) | 2007-03-28 | 2012-03-15 | Pharmacyclics, Inc. | Inhibitors of bruton's tyrosine kinase |
US20120101114A1 (en) | 2007-03-28 | 2012-04-26 | Pharmacyclics, Inc. | Inhibitors of bruton's tyrosine kinase |
EP2548558A1 (fr) | 2007-03-28 | 2013-01-23 | Pharmacyclics, Inc. | Composé hétérocyclique condensé contenant de l'azote comme inhibiteurs de la tyrosine kinase de bruton |
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 |
CA2702674C (fr) | 2007-10-19 | 2016-05-03 | Avila Therapeutics, Inc. | Composes heteroaryles et leurs utilisations |
US7989465B2 (en) | 2007-10-19 | 2011-08-02 | Avila Therapeutics, Inc. | 4,6-disubstituted pyrimidines useful as kinase inhibitors |
ES2444144T3 (es) | 2007-10-23 | 2014-02-24 | F. Hoffmann-La Roche Ag | Nuevos inhibidores de quinasa |
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 |
MX360970B (es) | 2008-06-27 | 2018-11-23 | Avila Therapeutics Inc | Compuestos de heteroarilo y usos de los mismos. |
CN102159214A (zh) | 2008-07-16 | 2011-08-17 | 药品循环公司 | 用于实体肿瘤的治疗的布鲁顿酪氨酸激酶的抑制剂 |
SG193859A1 (en) | 2008-09-05 | 2013-10-30 | Celgene Avilomics Res 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 |
KR20120093220A (ko) | 2009-09-16 | 2012-08-22 | 아빌라 테라퓨틱스, 인크. | 단백질 키나아제 컨쥬게이트 및 인히비터 |
US7718662B1 (en) | 2009-10-12 | 2010-05-18 | Pharmacyclics, Inc. | Pyrazolo-pyrimidine inhibitors of bruton's tyrosine kinase |
AU2011260961B9 (en) | 2010-05-31 | 2015-02-26 | Ono Pharmaceutical Co., Ltd. | Purinone derivative |
MY191929A (en) | 2010-06-03 | 2022-07-18 | Pharmacyclics Llc | The use of inhibitors of bruton's tyrosine kinase (btk) |
US20120071497A1 (en) | 2010-06-03 | 2012-03-22 | Pharmacyclics, Inc. | Methods of treating abc-dlbcl using inhibitors of bruton's tyrosine kinase |
AU2011269989B2 (en) | 2010-06-23 | 2014-12-11 | Hanmi Science Co., Ltd. | Novel fused pyrimidine derivatives for inhibition of tyrosine kinase activity |
EP2603081B1 (fr) | 2010-08-10 | 2016-10-05 | Celgene Avilomics Research, Inc. | Sel de bésylate d'un inhibiteur de btk |
HUE033019T2 (en) * | 2011-05-17 | 2017-11-28 | Principia Biopharma Inc | Tyrosine 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 |
US8501724B1 (en) | 2012-01-31 | 2013-08-06 | Pharmacyclics, Inc. | Purinone compounds as kinase inhibitors |
TWI662964B (zh) | 2012-06-04 | 2019-06-21 | 美商製藥有限責任公司 | 布魯頓氏酪胺酸激酶抑制劑之結晶形式 |
ES2776175T3 (es) * | 2012-06-18 | 2020-08-14 | Principia Biopharma Inc | Pirrolo- o pirazolopirimidinas covalentes reversibles útiles para el tratamiento de cáncer y enfermedades autoinmunes |
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) |
SG11201503842PA (en) * | 2012-11-15 | 2015-06-29 | Pharmacyclics Inc | Pyrrolopyrimidine compounds as kinase inhibitors |
SG11201509842SA (en) | 2013-05-30 | 2015-12-30 | Infinity Pharmaceuticals Inc | Treatment of cancers using pi3 kinase isoform modulators |
WO2015017812A1 (fr) | 2013-08-02 | 2015-02-05 | Pharmacyclics, Inc. | Méthodes permettant de traiter des tumeurs solides |
EA201690746A1 (ru) | 2013-10-25 | 2016-12-30 | Фармасайкликс Элэлси | Лечение с применением ингибиторов тирозинкиназы брутона и иммунотерапии |
CN106008516A (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 |
US9885086B2 (en) | 2014-03-20 | 2018-02-06 | Pharmacyclics Llc | Phospholipase C gamma 2 and resistance associated mutations |
-
2013
- 2013-11-14 SG SG11201503842PA patent/SG11201503842PA/en unknown
- 2013-11-14 BR BR112015011171A patent/BR112015011171A2/pt not_active IP Right Cessation
- 2013-11-14 MA MA38183A patent/MA38183A1/fr unknown
- 2013-11-14 EP EP13854424.2A patent/EP2920180A4/fr not_active Withdrawn
- 2013-11-14 EA EA201590855A patent/EA201590855A1/ru unknown
- 2013-11-14 MX MX2015006168A patent/MX2015006168A/es unknown
- 2013-11-14 KR KR1020157015148A patent/KR20150084923A/ko not_active Application Discontinuation
- 2013-11-14 CA CA2890934A patent/CA2890934A1/fr not_active Abandoned
- 2013-11-14 PE PE2015000625A patent/PE20151495A1/es not_active Application Discontinuation
- 2013-11-14 JP JP2015542791A patent/JP2015537033A/ja active Pending
- 2013-11-14 AU AU2013344656A patent/AU2013344656A1/en not_active Abandoned
- 2013-11-14 CN CN201380059811.2A patent/CN104854107A/zh active Pending
- 2013-11-14 WO PCT/US2013/070164 patent/WO2014078578A1/fr active Application Filing
- 2013-11-15 US US14/081,053 patent/US9096604B2/en active Active
- 2013-11-15 TW TW102141817A patent/TWI522359B/zh not_active IP Right Cessation
- 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 |
---|---|
EP2920180A4 (fr) | 2016-04-13 |
JP2015537033A (ja) | 2015-12-24 |
US20150239897A1 (en) | 2015-08-27 |
HK1215253A1 (zh) | 2016-08-19 |
PE20151495A1 (es) | 2015-10-23 |
AU2013344656A1 (en) | 2015-06-04 |
IL238728A0 (en) | 2015-06-30 |
AR093518A1 (es) | 2015-06-10 |
US9540385B2 (en) | 2017-01-10 |
US9096604B2 (en) | 2015-08-04 |
KR20150084923A (ko) | 2015-07-22 |
EP2920180A1 (fr) | 2015-09-23 |
US20160375026A1 (en) | 2016-12-29 |
CA2890934A1 (fr) | 2014-05-22 |
BR112015011171A2 (pt) | 2017-07-11 |
CR20150263A (es) | 2015-08-24 |
DOP2015000108A (es) | 2015-06-30 |
SG11201503842PA (en) | 2015-06-29 |
PH12015501067A1 (en) | 2015-08-10 |
NI201500067A (es) | 2016-02-15 |
US20140142126A1 (en) | 2014-05-22 |
CN104854107A (zh) | 2015-08-19 |
WO2014078578A1 (fr) | 2014-05-22 |
EA201590855A1 (ru) | 2015-11-30 |
TN2015000174A1 (en) | 2016-10-03 |
TWI522359B (zh) | 2016-02-21 |
CL2015001268A1 (es) | 2015-07-10 |
MX2015006168A (es) | 2015-08-10 |
TW201425315A (zh) | 2014-07-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
MA38183A1 (fr) | Composés pyrrolopyrimidines en tant qu'inhibiteurs de kinase | |
MA38961A1 (fr) | Composés 3-phenyl-1h-pyrazolo[3,4-d]pyrimidin-4-ylamine substitués inhibiteurs de la tyrosine kinase de bruton utilisés pour traiter par exemple les maladies auto-immunes, respiratoires et inflammatoires, cancer, mastocytose et osteoporose | |
TN2015000168A1 (fr) | Inhibiteurs de la tyrosine kinase de bruton | |
PH12014501815A1 (en) | Purinone compounds as kinase inhibitors | |
MA43094B1 (fr) | Dérivés de maytansinoïde, leurs conjugués, et procédés d'utilisation | |
MX2020010412A (es) | Inhibidores de tirosina quinasa de bruton. | |
LTPA2017009I1 (lt) | Brutono tirozinkinazės inhibitoriai | |
MA41654B2 (fr) | Formes cristallines d'un inhibiteur de tyrosine kinase de bruton | |
MA42622B1 (fr) | Agents de liaison à tigit et leurs utilisations | |
MA37829A1 (fr) | Combinaisons pharmaceutiques comprenant un inhibiteur de b-raf, un inhibiteur d'egfr et facultativement un inhibiteur de pi3k alpha | |
MA32226B1 (fr) | Compositions et leurs procedes de preparation et d'utilisation | |
MA38391A1 (fr) | Dérivés de pyridinyl et triazolone pyridinyl de fusion | |
MA38060A1 (fr) | Imidazo[1,2-a]pyridincarboxamides amino-substitués et leur utilisation | |
MA38273A1 (fr) | Thérapie de combinaison avec des anticorps anti-her3 | |
MA37742B1 (fr) | Dérivés d'oestra-1,3,5 (10), 16-tétraène substitués en position 3, leurs procédés de préparation, préparations pharmaceutiques les contenant, et leur utilisation pour la fabrication de médicaments | |
MA40791A (fr) | Ciblage lysosomal d'enzymes et utilisations associées | |
MA38925A1 (fr) | Dérivés de phénylalanine substitués | |
MA44909A (fr) | Association thérapeutique d'un inhibiteur du cd19 et d'un inhibiteur de la btk | |
MA35064B1 (fr) | Dérivés de thiéno[2,3-d]pyrimidine et leur utilisation pour traiter l'arythmie | |
MA38056B1 (fr) | Inhibiteurs de la tyrosine kinase de bruton | |
MA41643B1 (fr) | Formulations pharmaceutiques d'inhibiteur de la tyrosine kinase de bruton | |
MA41065B1 (fr) | Dérivés de maytansinoïde, conjugués de ceux-ci, et procédés d'utilisation | |
MA37678B2 (fr) | Nouvelles 7h-pyrrolo[2,3-d]pyrimidines substituées par un groupe amino en position 4, utilisées comme inhibiteurs de lrrk2 | |
MA37780B1 (fr) | Nouveaux acides 5-aminotétrahydrochinolino-2-carboxyliques et leur utilisation | |
EA202092370A1 (ru) | Новые модуляторы киназ |