MA38393A3 - Composés hétéroaryle et utilisations associées - Google Patents
Composés hétéroaryle et utilisations associéesInfo
- Publication number
- MA38393A3 MA38393A3 MA38393A MA38393A MA38393A3 MA 38393 A3 MA38393 A3 MA 38393A3 MA 38393 A MA38393 A MA 38393A MA 38393 A MA38393 A MA 38393A MA 38393 A3 MA38393 A3 MA 38393A3
- Authority
- MA
- Morocco
- Prior art keywords
- protein kinase
- heteroaryl compounds
- related uses
- compositions
- carcinomas
- 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- 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
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/78—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 2
- C07D239/80—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Gastroenterology & Hepatology (AREA)
- Neurology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Epidemiology (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Abstract
L'invention concerne des composés utiles comme inhibiteurs de protéines kinases, contenant un reste de cystéine dans le site de liaison atp. L'invention concerne également des compositions pharmaceutiquement acceptables comprenant des quantités thérapeutiquement efficaces d'un ou de plusieurs composés inhibiteurs de protéines kinases, ainsi que des méthodes d'utilisation de ces compositions dans le traitement de cancers et de carcinomes.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP14305361 | 2014-03-13 | ||
PCT/US2014/029270 WO2014144737A1 (fr) | 2013-03-15 | 2014-03-14 | Composés hétéroaryle et utilisations associées |
Publications (2)
Publication Number | Publication Date |
---|---|
MA38393A3 true MA38393A3 (fr) | 2018-05-31 |
MA38393B1 MA38393B1 (fr) | 2018-11-30 |
Family
ID=50390019
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA38393A MA38393B1 (fr) | 2014-03-13 | 2014-03-14 | Composés hétéroaryle et utilisations associées |
Country Status (13)
Country | Link |
---|---|
US (1) | US9663524B2 (fr) |
EP (1) | EP2968337B1 (fr) |
JP (1) | JP6576325B2 (fr) |
KR (1) | KR102219695B1 (fr) |
CN (2) | CN105307657B (fr) |
AU (1) | AU2014228746B2 (fr) |
BR (1) | BR112015022191A8 (fr) |
EA (1) | EA036160B1 (fr) |
MA (1) | MA38393B1 (fr) |
MX (1) | MX2015011514A (fr) |
PE (1) | PE20151776A1 (fr) |
SG (1) | SG11201507478VA (fr) |
WO (1) | WO2014144737A1 (fr) |
Families Citing this family (65)
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 |
GB201204384D0 (en) | 2012-03-13 | 2012-04-25 | Univ Dundee | Anti-flammatory agents |
ES2704744T3 (es) | 2012-06-13 | 2019-03-19 | Incyte Holdings Corp | Compuestos tricíclicos sustituidos como inhibidores de FGFR |
RS62233B1 (sr) | 2012-07-11 | 2021-09-30 | Blueprint Medicines Corp | Inhibitori receptora fibroblast faktora rasta |
WO2014026125A1 (fr) | 2012-08-10 | 2014-02-13 | Incyte Corporation | Dérivés de pyrazine en tant qu'inhibiteurs de fgfr |
US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
BR112015022191A8 (pt) | 2013-03-15 | 2018-01-23 | Celgene Avilomics Res Inc | compostos heteroarila e usos dos mesmos |
US9321786B2 (en) | 2013-03-15 | 2016-04-26 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
MY181020A (en) | 2013-03-15 | 2020-12-16 | Sanofi Sa | Heteroaryl compounds and uses thereof |
CN109776525B (zh) | 2013-04-19 | 2022-01-21 | 因赛特控股公司 | 作为fgfr抑制剂的双环杂环 |
SG11201602069WA (en) * | 2013-10-18 | 2016-04-28 | Eisai R&D Man Co Ltd | Pyrimidine fgfr4 inhibitors |
EP3060560A1 (fr) | 2013-10-25 | 2016-08-31 | Blueprint Medicines Corporation | Inhibiteurs du récepteur du facteur de croissance des fibroblastes |
AU2014338549B2 (en) | 2013-10-25 | 2017-05-25 | Novartis Ag | Ring-fused bicyclic pyridyl derivatives as FGFR4 inhibitors |
US9695165B2 (en) | 2014-01-15 | 2017-07-04 | Blueprint Medicines Corporation | Inhibitors of the fibroblast growth factor receptor |
EP3171874B1 (fr) | 2014-07-21 | 2020-11-18 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs d'imidazolyl kinase et leurs utilisations |
DK3172213T3 (da) | 2014-07-21 | 2021-12-13 | Dana Farber Cancer Inst Inc | Makrocykliske kinasehæmmere og anvendelser deraf |
AU2015300782B2 (en) | 2014-08-08 | 2020-04-16 | Dana-Farber Cancer Institute, Inc. | Uses of salt-inducible kinase (SIK) inhibitors |
WO2016054483A1 (fr) | 2014-10-03 | 2016-04-07 | Novartis Ag | Utilisation de dérivés pyridyle bicycliques à anneaux fusionnés en tant qu'inhibiteurs de fgfr4 |
US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
US9580423B2 (en) | 2015-02-20 | 2017-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
AU2016219822B2 (en) | 2015-02-20 | 2020-07-09 | Incyte Holdings Corporation | Bicyclic heterocycles as FGFR inhibitors |
MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
AU2016238436A1 (en) | 2015-03-25 | 2017-08-17 | Novartis Ag | Formylated N-heterocyclic derivatives as FGFR4 inhibitors |
US9802917B2 (en) | 2015-03-25 | 2017-10-31 | Novartis Ag | Particles of N-(5-cyano-4-((2-methoxyethyl)amino)pyridin-2-yl)-7-formyl-6-((4-methyl-2-oxopiperazin-1-yl)methyl)-3,4-dihydro-1,8-naphthyridine-1(2H)-carboxamide |
WO2016168331A1 (fr) | 2015-04-14 | 2016-10-20 | Eisai R&D Management Co., Ltd. | Composé inhibiteur de fgfr4 cristallin et utilisations de celui-ci |
JP7372740B2 (ja) | 2016-05-10 | 2023-11-01 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 細胞生存性及び/又は細胞増殖を低減するための薬物の組み合わせ |
KR20180002053A (ko) * | 2016-06-28 | 2018-01-05 | 한미약품 주식회사 | 신규한 헤테로시클릭 유도체 화합물 및 이의 용도 |
AU2017291812B2 (en) | 2016-07-05 | 2023-12-14 | Dana-Farber Cancer Institute, Inc. | Bicyclic urea kinase inhibitors and uses thereof |
US11241435B2 (en) | 2016-09-16 | 2022-02-08 | The General Hospital Corporation | Uses of salt-inducible kinase (SIK) inhibitors for treating osteoporosis |
WO2018055503A1 (fr) | 2016-09-20 | 2018-03-29 | Novartis Ag | Combinaison comprenant un antagoniste de pd-1 et un inhibiteur de fgfr4 |
CN109922804B (zh) | 2016-11-02 | 2023-11-17 | 诺华股份有限公司 | Fgfr4抑制剂和胆汁酸螯合剂的组合 |
JP6919922B2 (ja) * | 2016-12-19 | 2021-08-18 | アビスコ セラピューティクス カンパニー リミテッド | Fgfr4阻害剤、その製造方法と薬学的な応用 |
CN108503593B (zh) * | 2017-02-28 | 2021-04-27 | 暨南大学 | 2-氨基嘧啶类化合物及其应用 |
BR112019017741A2 (pt) | 2017-02-28 | 2020-04-07 | Dana Farber Cancer Inst Inc | usos de pirimidopirimidinonas como inibidores de sik |
US11174255B2 (en) * | 2017-05-15 | 2021-11-16 | University Of Houston System | Pyrido[2,3-d]pyrimidin-7-ones and related compounds as inhibitors of protein kinases |
AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
CN110914267B (zh) * | 2017-07-19 | 2022-07-12 | 江苏奥赛康药业有限公司 | 嘧啶并吡啶酮或者吡啶并吡啶酮类化合物及其应用 |
CN109384790B (zh) * | 2017-08-08 | 2022-05-10 | 药捷安康(南京)科技股份有限公司 | 成纤维细胞生长因子受体抑制剂及其用途 |
CN109745325B (zh) * | 2017-11-08 | 2022-02-15 | 上海翰森生物医药科技有限公司 | Fgfr4抑制剂、其制备方法和用途 |
CN110386921A (zh) * | 2018-04-23 | 2019-10-29 | 南京药捷安康生物科技有限公司 | 成纤维细胞生长因子受体抑制剂化合物 |
BR112020022392A2 (pt) | 2018-05-04 | 2021-02-02 | Incyte Corporation | formas sólidas de um inibidor de fgfr e processos para preparação das mesmas |
MX2020011639A (es) | 2018-05-04 | 2021-02-15 | Incyte Corp | Sales de un inhibidor de receptores de factor de crecimiento de fibroblastos (fgfr). |
WO2019223766A1 (fr) * | 2018-05-25 | 2019-11-28 | 上海和誉生物医药科技有限公司 | Inhibiteur de fgfr, son procédé de préparation et son utilisation pharmaceutique |
CN110577524B (zh) * | 2018-06-07 | 2022-01-28 | 北京大学深圳研究生院 | 一种激酶选择性抑制剂 |
CN111936493B (zh) * | 2018-06-19 | 2023-05-26 | 上海和誉生物医药科技有限公司 | 一种高选择性FGFRi抑制剂及其制备方法和应用 |
CN112119064B (zh) | 2018-09-14 | 2023-06-23 | 上海和誉生物医药科技有限公司 | Fgfr抑制剂、其制备方法和应用 |
WO2020177067A1 (fr) | 2019-03-05 | 2020-09-10 | Bioardis Llc | Dérivés aromatiques, procédés de préparation et utilisations médicales de ceux-ci |
WO2020185532A1 (fr) | 2019-03-08 | 2020-09-17 | Incyte Corporation | Méthodes de traitement du cancer au moyen d'un inhibiteur de fgfr |
EP3936509B1 (fr) * | 2019-03-08 | 2024-07-31 | Shouyao Holdings (Beijing) Co., Ltd. | Inhibiteur de fgfr4 kinase, son procédé de préparation et son utilisation |
US11591329B2 (en) | 2019-07-09 | 2023-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
IL291901A (en) | 2019-10-14 | 2022-06-01 | Incyte Corp | Bicyclyl heterocycles as fgr suppressors |
WO2021076728A1 (fr) | 2019-10-16 | 2021-04-22 | Incyte Corporation | Hétérocycles bicycliques en tant qu'inhibiteurs de fgfr |
GB201915828D0 (en) * | 2019-10-31 | 2019-12-18 | Cancer Research Tech Ltd | Compounds, compositions and therapeutic uses thereof |
WO2021108803A1 (fr) | 2019-11-26 | 2021-06-03 | Theravance Biopharma R&D Ip, Llc | Composés de pyrimidine pyridinone fusionnés en tant qu'inhibiteurs de jak |
KR20220131900A (ko) | 2019-12-04 | 2022-09-29 | 인사이트 코포레이션 | Fgfr 억제제의 유도체 |
WO2021113479A1 (fr) | 2019-12-04 | 2021-06-10 | Incyte Corporation | Hétérocycles tricycliques en tant qu'inhibiteurs de fgfr |
WO2021146424A1 (fr) | 2020-01-15 | 2021-07-22 | Incyte Corporation | Hétérocycles bicycliques en tant qu'inhibiteurs de fgfr |
KR102382613B1 (ko) * | 2020-01-15 | 2022-04-06 | 한국과학기술연구원 | 단백질 키나아제 저해 활성을 갖는 7-아미노-3,4-디히드로피리미도피리미딘-2-온 유도체 및 이를 포함하는 치료용 약학 조성물 |
AU2021436754A1 (en) * | 2021-03-26 | 2023-10-12 | Apeloa Pharmaceutical Co., Ltd. | Bicyclic heterocyclic fgfr4 inhibitor, pharmaceutical composition and preparation comprising same, and application thereof |
CA3215903A1 (fr) | 2021-04-12 | 2022-10-20 | Incyte Corporation | Polytherapie comprenant un inhibiteur de fgfr et un agent de ciblage de nectine-4 |
EP4352059A1 (fr) | 2021-06-09 | 2024-04-17 | Incyte Corporation | Hétérocycles tricycliques en tant qu'inhibiteurs de fgfr |
CN113527311B (zh) * | 2021-08-23 | 2022-05-06 | 中南大学湘雅医院 | Fgfr4抑制剂、组合物及其在药物制备中的用途 |
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-
2014
- 2014-03-14 BR BR112015022191A patent/BR112015022191A8/pt active Search and Examination
- 2014-03-14 SG SG11201507478VA patent/SG11201507478VA/en unknown
- 2014-03-14 MX MX2015011514A patent/MX2015011514A/es active IP Right Grant
- 2014-03-14 WO PCT/US2014/029270 patent/WO2014144737A1/fr active Application Filing
- 2014-03-14 CN CN201480016170.7A patent/CN105307657B/zh active Active
- 2014-03-14 CN CN202010661205.XA patent/CN111793068A/zh active Pending
- 2014-03-14 PE PE2015002022A patent/PE20151776A1/es unknown
- 2014-03-14 MA MA38393A patent/MA38393B1/fr unknown
- 2014-03-14 EP EP14763001.6A patent/EP2968337B1/fr active Active
- 2014-03-14 EA EA201591420A patent/EA036160B1/ru not_active IP Right Cessation
- 2014-03-14 KR KR1020157029048A patent/KR102219695B1/ko active IP Right Grant
- 2014-03-14 JP JP2016503031A patent/JP6576325B2/ja active Active
- 2014-03-14 AU AU2014228746A patent/AU2014228746B2/en not_active Ceased
- 2014-03-14 US US14/776,373 patent/US9663524B2/en active Active
Also Published As
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SG11201507478VA (en) | 2015-10-29 |
MX2015011514A (es) | 2016-08-11 |
BR112015022191A8 (pt) | 2018-01-23 |
CN105307657A (zh) | 2016-02-03 |
CN111793068A (zh) | 2020-10-20 |
BR112015022191A2 (pt) | 2017-10-10 |
PE20151776A1 (es) | 2015-12-11 |
JP2016519673A (ja) | 2016-07-07 |
AU2014228746A1 (en) | 2015-09-10 |
EP2968337A4 (fr) | 2016-10-19 |
WO2014144737A1 (fr) | 2014-09-18 |
EP2968337B1 (fr) | 2021-07-21 |
AU2014228746B2 (en) | 2018-08-30 |
KR20150131237A (ko) | 2015-11-24 |
MA38393B1 (fr) | 2018-11-30 |
KR102219695B1 (ko) | 2021-02-25 |
EP2968337A1 (fr) | 2016-01-20 |
US20160046634A1 (en) | 2016-02-18 |
JP6576325B2 (ja) | 2019-09-18 |
EA036160B1 (ru) | 2020-10-08 |
EA201591420A1 (ru) | 2016-02-29 |
CN105307657B (zh) | 2020-07-10 |
US9663524B2 (en) | 2017-05-30 |
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