MA51429A - Dérivés amino-fluoropipéridines utilisés en tant qu'inhibiteur de kinase - Google Patents
Dérivés amino-fluoropipéridines utilisés en tant qu'inhibiteur de kinaseInfo
- Publication number
- MA51429A MA51429A MA051429A MA51429A MA51429A MA 51429 A MA51429 A MA 51429A MA 051429 A MA051429 A MA 051429A MA 51429 A MA51429 A MA 51429A MA 51429 A MA51429 A MA 51429A
- Authority
- MA
- Morocco
- Prior art keywords
- amino
- kinase inhibitor
- derivatives used
- fluoropiperidine
- fluoropiperidine derivatives
- Prior art date
Links
- XTWMFWPWKJBNDS-UHFFFAOYSA-N 1-fluoropiperidin-2-amine Chemical class NC1N(CCCC1)F XTWMFWPWKJBNDS-UHFFFAOYSA-N 0.000 title 1
- 229940043355 kinase inhibitor Drugs 0.000 title 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 title 1
Classifications
-
- 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
- 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
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (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)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1020170183060A KR102577241B1 (ko) | 2017-12-28 | 2017-12-28 | 카이네이즈 저해제로서의 아미노-플루오로피페리딘 유도체 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA51429A true MA51429A (fr) | 2021-04-07 |
Family
ID=67063980
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA051429A MA51429A (fr) | 2017-12-28 | 2018-12-28 | Dérivés amino-fluoropipéridines utilisés en tant qu'inhibiteur de kinase |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US11078206B2 (fr) |
| EP (1) | EP3733671B1 (fr) |
| JP (1) | JP7032535B2 (fr) |
| KR (1) | KR102577241B1 (fr) |
| CN (1) | CN111491934B (fr) |
| AU (1) | AU2018394995B2 (fr) |
| BR (1) | BR112020013164A2 (fr) |
| CA (1) | CA3084777C (fr) |
| CL (1) | CL2020001754A1 (fr) |
| DO (1) | DOP2020000109A (fr) |
| EC (1) | ECSP20035222A (fr) |
| ES (1) | ES2923682T3 (fr) |
| MA (1) | MA51429A (fr) |
| MX (1) | MX2020006708A (fr) |
| MY (1) | MY196186A (fr) |
| PE (1) | PE20210548A1 (fr) |
| PH (1) | PH12020551014A1 (fr) |
| RU (1) | RU2762637C1 (fr) |
| SA (1) | SA520412333B1 (fr) |
| SG (1) | SG11202004918XA (fr) |
| TN (1) | TN2020000125A1 (fr) |
| WO (1) | WO2019132560A1 (fr) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104263816B (zh) | 2008-05-16 | 2018-10-19 | 生命技术公司 | 用于测量细胞增殖的双标记法 |
| EP3652169A1 (fr) | 2017-08-01 | 2020-05-20 | Theravance Biopharma R&D IP, LLC | Composés bicycliques pyrazolo et triazolo utilisés en tant qu'inhibiteurs de kinase jak |
| PL3733673T3 (pl) | 2017-12-28 | 2022-09-26 | Daewoong Pharmaceutical Co., Ltd. | Pochodna oksyfluoropiperydyny jako inhibitor kinazy |
| KR102577242B1 (ko) | 2017-12-28 | 2023-09-11 | 주식회사 대웅제약 | 카이네이즈 저해제로서의 아미노-메틸피페리딘 유도체 |
| JP2022518741A (ja) | 2019-01-23 | 2022-03-16 | セラヴァンス バイオファーマ アール＆ディー アイピー， エルエルシー | ＪＡＫキナーゼ阻害剤としてのイミダゾ［１，５－ａ］ピリジン、１，２，４－トリアゾロ［４，３－ａ］ピリジンおよびイミダゾ［１，５－ａ］ピラジン |
| SMT202500339T1 (it) | 2019-09-23 | 2025-11-10 | Pmv Pharmaceuticals Inc | Metodi e composti per ripristinare la funzione di p53 mutante |
| 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 |
| CN115023428B (zh) * | 2020-01-21 | 2025-04-08 | 江苏先声药业有限公司 | 嘧啶并吡咯类化合物 |
| CN115244055B (zh) * | 2020-01-21 | 2024-09-03 | 江苏先声药业有限公司 | 嘧啶并五元环类衍生物及其应用 |
| US12570645B2 (en) | 2020-06-22 | 2026-03-10 | Pmv Pharmaceuticals, Inc. | Uses of p53 x-ray co-crystal structures |
| CA3183025A1 (fr) | 2020-06-24 | 2021-12-30 | Melissa Dumble | Outil de diagnostic compagnon pour composes de reactivation de p53 mutantes |
| WO2021262484A1 (fr) | 2020-06-24 | 2021-12-30 | Pmv Pharmaceuticals, Inc. | Polythérapie pour le traitement du cancer |
| WO2022062601A1 (fr) * | 2020-09-22 | 2022-03-31 | 江苏先声药业有限公司 | Composé pyrimidopyrrole |
| CN114315838B (zh) * | 2020-09-30 | 2024-09-03 | 江苏先声药业有限公司 | 嘧啶并吡咯类化合物 |
| AU2023213949A1 (en) | 2022-01-27 | 2024-07-25 | Pmv Pharmaceuticals, Inc. | Deuterated compounds for restoring mutant p53 function |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7301023B2 (en) | 2001-05-31 | 2007-11-27 | Pfizer Inc. | Chiral salt resolution |
| CA2730930C (fr) | 2008-07-16 | 2015-01-13 | Pharmacyclics, Inc. | Inhibiteurs de tyrosine kinase de bruton pour le traitement de tumeurs solides |
| JP5918693B2 (ja) * | 2009-05-05 | 2016-05-18 | ダナ ファーバー キャンサー インスティテュート インコーポレイテッド | Ｅｇｆｒ阻害剤及び疾患の治療方法 |
| CA2803056C (fr) * | 2010-06-23 | 2017-05-16 | Hanmi Science Co., Ltd. | Derives de pyrimidine fusionnes destines a l'inhibition de l'activite tyrosine kynase |
| ES2575710T3 (es) * | 2011-09-22 | 2016-06-30 | Pfizer Inc | Derivados de pirrolopirimidina y purina |
| ES2733576T3 (es) * | 2012-08-06 | 2019-12-02 | Acea Therapeutics Inc | Nuevos compuestos de pirrolopirimidina como inhibidores de proteína cinasas |
| US9840517B2 (en) | 2013-09-18 | 2017-12-12 | Beijing Hanmi Pharmaceutical Co., Ltd. | Compound inhibiting activities of BTK and/or JAK3 kinases |
| ES2654051T3 (es) | 2013-12-05 | 2018-02-12 | Pfizer Inc. | Pirrolo[2,3-d]pirimidinilo, pirrolo[2,3-b]pirazinilo y pirrolo[2,3-d]piridinil acrilamidas |
| CN105732637B (zh) * | 2014-12-30 | 2020-04-21 | 广东东阳光药业有限公司 | 杂芳化合物及其在药物中的应用 |
| 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 |
| KR102329162B1 (ko) * | 2016-06-30 | 2021-11-22 | 주식회사 대웅제약 | 카이네이즈 저해제로서의 피라졸로피리미딘 유도체 |
| KR102032418B1 (ko) | 2017-06-15 | 2019-10-16 | 한국화학연구원 | 접합 피리미딘 유도체, 이의 제조방법 및 이를 유효성분으로 포함하는 브루톤티로신 키나제 활성 관련 질환의 예방 또는 치료용 약학적 조성물 |
-
2017
- 2017-12-28 KR KR1020170183060A patent/KR102577241B1/ko active Active
-
2018
- 2018-12-28 MX MX2020006708A patent/MX2020006708A/es unknown
- 2018-12-28 MA MA051429A patent/MA51429A/fr unknown
- 2018-12-28 MY MYPI2020002995A patent/MY196186A/en unknown
- 2018-12-28 ES ES18894845T patent/ES2923682T3/es active Active
- 2018-12-28 RU RU2020124577A patent/RU2762637C1/ru active
- 2018-12-28 JP JP2020532550A patent/JP7032535B2/ja active Active
- 2018-12-28 EP EP18894845.9A patent/EP3733671B1/fr active Active
- 2018-12-28 AU AU2018394995A patent/AU2018394995B2/en active Active
- 2018-12-28 BR BR112020013164-4A patent/BR112020013164A2/pt unknown
- 2018-12-28 PE PE2020000773A patent/PE20210548A1/es unknown
- 2018-12-28 SG SG11202004918XA patent/SG11202004918XA/en unknown
- 2018-12-28 CN CN201880081900.XA patent/CN111491934B/zh active Active
- 2018-12-28 CA CA3084777A patent/CA3084777C/fr active Active
- 2018-12-28 WO PCT/KR2018/016812 patent/WO2019132560A1/fr not_active Ceased
- 2018-12-28 TN TNP/2020/000125A patent/TN2020000125A1/en unknown
- 2018-12-28 US US16/770,642 patent/US11078206B2/en active Active
-
2020
- 2020-06-10 DO DO2020000109A patent/DOP2020000109A/es unknown
- 2020-06-25 SA SA520412333A patent/SA520412333B1/ar unknown
- 2020-06-26 EC ECSENADI202035222A patent/ECSP20035222A/es unknown
- 2020-06-26 CL CL2020001754A patent/CL2020001754A1/es unknown
- 2020-06-28 PH PH12020551014A patent/PH12020551014A1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP3733671A4 (fr) | 2021-06-09 |
| PH12020551014A1 (en) | 2021-08-16 |
| KR20190080540A (ko) | 2019-07-08 |
| EP3733671B1 (fr) | 2022-06-29 |
| NZ765159A (en) | 2023-09-29 |
| US11078206B2 (en) | 2021-08-03 |
| KR102577241B1 (ko) | 2023-09-11 |
| JP7032535B2 (ja) | 2022-03-08 |
| CN111491934A (zh) | 2020-08-04 |
| DOP2020000109A (es) | 2020-09-30 |
| AU2018394995B2 (en) | 2021-05-13 |
| CA3084777C (fr) | 2022-08-30 |
| PE20210548A1 (es) | 2021-03-17 |
| US20200299298A1 (en) | 2020-09-24 |
| SG11202004918XA (en) | 2020-06-29 |
| CA3084777A1 (fr) | 2019-07-04 |
| CL2020001754A1 (es) | 2020-11-27 |
| AU2018394995A1 (en) | 2020-06-25 |
| MY196186A (en) | 2023-03-21 |
| RU2762637C1 (ru) | 2021-12-21 |
| EP3733671A1 (fr) | 2020-11-04 |
| ECSP20035222A (es) | 2020-07-31 |
| CN111491934B (zh) | 2022-08-30 |
| ES2923682T3 (es) | 2022-09-29 |
| JP2021505644A (ja) | 2021-02-18 |
| SA520412333B1 (ar) | 2022-12-08 |
| BR112020013164A2 (pt) | 2020-12-01 |
| MX2020006708A (es) | 2020-08-20 |
| WO2019132560A1 (fr) | 2019-07-04 |
| TN2020000125A1 (en) | 2022-01-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP3733671A4 (fr) | Dérivés amino-fluoropipéridines utilisés en tant qu'inhibiteur de kinase | |
| MA51431A (fr) | Dérivés d'oxy-fluoropipéridine utilisés en tant qu'inhibiteur de kinase | |
| MA47125A (fr) | Dérivés de pyrazole en tant qu'inhibiteurs de malt1 | |
| MA52486A (fr) | Pyridazinones utilisés en tant qu'inhibiteurs de parp7 | |
| MA54076A (fr) | 2-amino-n-hétéroaryl-nicotinamides utilisés en tant qu'inhibiteurs de nav1.8 | |
| EP3873468A4 (fr) | 2-amino-n-phényl-nicotinamides utilisés en tant qu'inhibiteurs de nav1.8 | |
| MA49888A (fr) | Composés macrocycliques utilisés en tant qu'inhibiteurs de kinase ros1 | |
| MA42659A (fr) | Dérivés hétéroaryle utilisés en tant qu'inhibiteurs de parp | |
| EP3656769A4 (fr) | Composé aryl-phosphore-oxygène utilisé en tant qu'inhibiteur de kinase egfr | |
| MA47120A (fr) | Dérivés pyridine utilisés en tant qu'immunomodulateurs | |
| MA47460A (fr) | Aminotriazolopyridines utilisées en tant qu'inhibiteurs de kinase | |
| EP3719012A4 (fr) | Composé uracile utilisé en tant qu'inhibiteur de c-met/axl | |
| EP3416964A4 (fr) | Dérivés de carboxamide utiles en tant qu'inhibiteurs de rsk | |
| MA43169A (fr) | Composés hétérocycliques utilisés en tant qu'inhibiteurs de pi3k-gamma | |
| MA45153A (fr) | Dérivés de carbonucléosides substitués utiles en tant qu'agents anticancéreux | |
| MA49374A (fr) | Composés hétéroaromatiques utilisés en tant qu'inhibiteurs de vanine | |
| MA40774A (fr) | Dérivés de diaryle-urée en tant qu'inhibiteurs de kinase p38 | |
| MA51438A (fr) | Composés hétérocycliques utilisés en tant qu'inhibiteurs de lsd1 | |
| EP3533787A4 (fr) | Composé de pyridone en tant qu'inhibiteur de c-met | |
| MA47013A (fr) | Composés benzolactames utilisés en tant qu'inhibiteurs de protéine kinase | |
| EP3697787A4 (fr) | Composé hétérocyclique à utiliser en tant qu'inhibiteur de protéine kinase | |
| MA51433A (fr) | Dérivé d'amino-méthyl pipéridine en tant qu'inhibiteur de kinase | |
| MA47086A (fr) | Dérivés de dihydropyrimidine-carboxamide bicycliques utilisés en tant qu'inhibiteurs de rho-kinase | |
| MA45375A (fr) | Composés hétérocycliques utilisés en tant qu'agents antibacteriens | |
| MA46981A (fr) | Dérivés de benzimidazole en tant qu'inhibiteurs de bromodomaine |