SG11201811470PA - Pyrazolopyrimidine derivatives as kinase inhibitor - Google Patents
Pyrazolopyrimidine derivatives as kinase inhibitorInfo
- Publication number
- SG11201811470PA SG11201811470PA SG11201811470PA SG11201811470PA SG11201811470PA SG 11201811470P A SG11201811470P A SG 11201811470PA SG 11201811470P A SG11201811470P A SG 11201811470PA SG 11201811470P A SG11201811470P A SG 11201811470PA SG 11201811470P A SG11201811470P A SG 11201811470PA
- Authority
- SG
- Singapore
- Prior art keywords
- international
- gyeonggi
- yongin
- gil
- seoul
- Prior art date
Links
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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene
-
- 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
- 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
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- 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
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR20160083050 | 2016-06-30 | ||
| PCT/KR2017/006980 WO2018004306A1 (en) | 2016-06-30 | 2017-06-30 | Pyrazolopyrimidine derivatives as kinase inhibitor |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SG11201811470PA true SG11201811470PA (en) | 2019-01-30 |
Family
ID=60785389
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SG11201811470PA SG11201811470PA (en) | 2016-06-30 | 2017-06-30 | Pyrazolopyrimidine derivatives as kinase inhibitor |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US10961247B2 (ko) |
| EP (2) | EP3950691A1 (ko) |
| JP (2) | JP2019519579A (ko) |
| KR (1) | KR102329162B1 (ko) |
| CN (2) | CN113135920A (ko) |
| AU (1) | AU2017287762C1 (ko) |
| BR (1) | BR112018074621B1 (ko) |
| CA (1) | CA3025636C (ko) |
| CL (1) | CL2018003511A1 (ko) |
| CO (1) | CO2018013293A2 (ko) |
| DO (1) | DOP2018000275A (ko) |
| EC (1) | ECSP18093777A (ko) |
| IL (1) | IL263306B (ko) |
| MX (2) | MX2021009378A (ko) |
| MY (1) | MY191110A (ko) |
| PE (1) | PE20190811A1 (ko) |
| PH (1) | PH12018502507A1 (ko) |
| RU (1) | RU2714206C1 (ko) |
| SA (2) | SA518400547B1 (ko) |
| SG (1) | SG11201811470PA (ko) |
| WO (1) | WO2018004306A1 (ko) |
| ZA (1) | ZA201808431B (ko) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP7098716B2 (ja) | 2017-08-01 | 2022-07-11 | 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ピラゾロおよびトリアゾロ二環式化合物 |
| LT3733673T (lt) | 2017-12-28 | 2022-08-10 | Daewoong Pharmaceutical Co., Ltd. | Oksi-fluorpiperidino darinys, kaip kinazės inhibitorius |
| KR102577241B1 (ko) * | 2017-12-28 | 2023-09-11 | 주식회사 대웅제약 | 카이네이즈 저해제로서의 아미노-플루오로피페리딘 유도체 |
| KR102577242B1 (ko) * | 2017-12-28 | 2023-09-11 | 주식회사 대웅제약 | 카이네이즈 저해제로서의 아미노-메틸피페리딘 유도체 |
| CN108586341B (zh) * | 2018-05-25 | 2020-05-08 | 天津商业大学 | 酰胺类化合物和其药用盐及其制备方法和药物用途 |
| EP3833350A4 (en) | 2018-08-10 | 2022-05-18 | Aclaris Therapeutics, Inc. | PYRROLOPYRIMIDINE TKI INHIBITORS |
| US10851102B2 (en) | 2019-01-23 | 2020-12-01 | Theravance Biopharma R&D Ip, Llc | Imidazole and triazole containing bicyclic compounds as JAK inhibitors |
| WO2020187267A1 (zh) * | 2019-03-18 | 2020-09-24 | 上海海雁医药科技有限公司 | Btk抑制剂及其药学上可接受的盐和多晶型物及其应用 |
| CN110317176A (zh) * | 2019-07-04 | 2019-10-11 | 沈阳药科大学 | 2-氨基嘧啶类化合物及其用途 |
| CN114901659A (zh) | 2019-11-26 | 2022-08-12 | 施万生物制药研发Ip有限责任公司 | 作为jak抑制剂的稠合嘧啶吡啶酮化合物 |
| CN113214265B (zh) * | 2020-01-21 | 2023-07-07 | 江苏先声药业有限公司 | 嘧啶并五元环类化合物 |
| WO2021147953A1 (zh) * | 2020-01-21 | 2021-07-29 | 江苏先声药业有限公司 | 嘧啶并五元环类衍生物及其应用 |
| CN115023428A (zh) * | 2020-01-21 | 2022-09-06 | 江苏先声药业有限公司 | 嘧啶并吡咯类化合物 |
| CN111620878A (zh) * | 2020-06-10 | 2020-09-04 | 中国药科大学 | 吡咯并嘧啶类衍生物作为蛋白激酶抑制剂及其应用 |
| TW202202498A (zh) * | 2020-07-01 | 2022-01-16 | 大陸商四川海思科製藥有限公司 | 一種並環雜環衍生物及其在醫藥上的應用 |
| WO2022062601A1 (zh) * | 2020-09-22 | 2022-03-31 | 江苏先声药业有限公司 | 嘧啶并吡咯类化合物 |
| CN114315838A (zh) * | 2020-09-30 | 2022-04-12 | 江苏先声药业有限公司 | 嘧啶并吡咯类化合物 |
| WO2022140246A1 (en) | 2020-12-21 | 2022-06-30 | Hangzhou Jijing Pharmaceutical Technology Limited | Methods and compounds for targeted autophagy |
| WO2023242597A1 (en) * | 2022-06-16 | 2023-12-21 | Amphista Therapeutics Limited | Bifunctional molecules for targeted protein degradation |
| CN115368366A (zh) * | 2022-08-02 | 2022-11-22 | 江苏省中医药研究院 | 嘧啶并吡唑类化合物及其应用 |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7301023B2 (en) | 2001-05-31 | 2007-11-27 | Pfizer Inc. | Chiral salt resolution |
| NZ535748A (en) | 2002-04-12 | 2007-06-29 | Pfizer | Use of EP4 receptor ligands in the treatment of IL-6 involved diseases |
| KR20080026654A (ko) | 2005-07-14 | 2008-03-25 | 아스텔라스세이야쿠 가부시키가이샤 | 헤테로시클릭 야누스 키나제 3 억제제 |
| MY162590A (en) | 2005-12-13 | 2017-06-30 | Incyte Holdings Corp | Heteroaryl substituted pyrrolo[2,3-b] pyridines and pyrrolo[2,3-b] pyrimidines as janus kinase inhibitors |
| EP2081435B1 (en) | 2006-09-22 | 2016-05-04 | Pharmacyclics LLC | Inhibitors of bruton's tyrosine kinase |
| US20100190777A1 (en) | 2007-07-17 | 2010-07-29 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| WO2009026107A1 (en) * | 2007-08-17 | 2009-02-26 | Portola Pharmaceuticals, Inc. | Protein kinase inhibitors |
| WO2009054941A1 (en) | 2007-10-25 | 2009-04-30 | Merck & Co., Inc. | Therapeutic compounds |
| EP2271631B1 (en) | 2008-04-22 | 2018-07-04 | Portola Pharmaceuticals, Inc. | Inhibitors of protein kinases |
| PE20091846A1 (es) * | 2008-05-19 | 2009-12-16 | Plexxikon Inc | DERIVADOS DE PIRROLO[2,3-d]-PIRIMIDINA COMO MODULADORES DE CINASAS |
| EP3311818A3 (en) | 2008-07-16 | 2018-07-18 | Pharmacyclics, LLC | Inhibitors of bruton's tyrosine kinase for the treatment of solid tumors |
| CN102482277B (zh) | 2009-05-05 | 2017-09-19 | 达纳-法伯癌症研究所有限公司 | 表皮生长因子受体抑制剂及治疗障碍的方法 |
| PE20130005A1 (es) | 2009-12-01 | 2013-02-16 | Abbvie Inc | Compuestos triciclicos novedosos |
| BR112012033253A2 (pt) | 2010-06-23 | 2016-11-22 | Hanmi Science Co Ltd | novos derivados de pirimidina fundidos para inibição da atividade de tirosina quinase |
| WO2013041042A1 (en) | 2011-09-22 | 2013-03-28 | Merck Sharp & Dohme Corp. | Pyrazole carboxamides as janus kinase inhibitors |
| WO2013169401A1 (en) * | 2012-05-05 | 2013-11-14 | Ariad Pharmaceuticals, Inc. | Compounds for inhibiting cell proliferation in egfr-driven cancers |
| EP2964647A1 (en) | 2013-03-05 | 2016-01-13 | F. Hoffmann-La Roche AG | Inhibitors of bruton's tyrosine kinase |
| CN117486865A (zh) | 2013-07-11 | 2024-02-02 | 艾森医药公司 | 嘧啶衍生物作为激酶抑制剂 |
| CN106065017B (zh) * | 2013-09-18 | 2018-06-01 | 北京韩美药品有限公司 | 抑制btk和/或jak3激酶活性的化合物 |
| SI3318565T1 (sl) * | 2013-12-05 | 2021-07-30 | Pfizer Inc. | Pirolo(2,3-D)pirimidinil, pirolo(2,3-B)pirazinil in pirolo(2,3-D)piridinil akrilamidi |
| WO2016000615A1 (en) * | 2014-07-02 | 2016-01-07 | Sunshine Lake Pharma Co., Ltd. | Heteroaryl compounds and pharmaceutical applications thereof |
| CN105315285B (zh) * | 2014-07-25 | 2017-12-08 | 上海海雁医药科技有限公司 | 2,4‑二取代7H‑吡咯并[2,3‑d]嘧啶衍生物、其制法与医药上的用途 |
| KR101710127B1 (ko) | 2014-08-29 | 2017-02-27 | 한화제약주식회사 | 야누스인산화효소 억제제로서의 치환된 N-(피롤리딘-3-일)-7H-피롤로[2,3-d]피리미딘-4-아민 |
| 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 |
| EP3778604A1 (en) | 2015-02-13 | 2021-02-17 | Dana Farber Cancer Institute, Inc. | Lrrk2 inhibitors and methods of making and using the same |
-
2017
- 2017-06-30 EP EP21190933.8A patent/EP3950691A1/en active Pending
- 2017-06-30 EP EP17820582.9A patent/EP3478687B1/en active Active
- 2017-06-30 MY MYPI2018002167A patent/MY191110A/en unknown
- 2017-06-30 CA CA3025636A patent/CA3025636C/en active Active
- 2017-06-30 PE PE2018003174A patent/PE20190811A1/es unknown
- 2017-06-30 US US16/304,798 patent/US10961247B2/en active Active
- 2017-06-30 CN CN202110351304.2A patent/CN113135920A/zh active Pending
- 2017-06-30 CN CN201780039336.0A patent/CN109311896B/zh active Active
- 2017-06-30 SG SG11201811470PA patent/SG11201811470PA/en unknown
- 2017-06-30 AU AU2017287762A patent/AU2017287762C1/en active Active
- 2017-06-30 MX MX2021009378A patent/MX2021009378A/es unknown
- 2017-06-30 KR KR1020170083259A patent/KR102329162B1/ko active IP Right Grant
- 2017-06-30 BR BR112018074621-5A patent/BR112018074621B1/pt active IP Right Grant
- 2017-06-30 MX MX2018016287A patent/MX2018016287A/es unknown
- 2017-06-30 JP JP2018568407A patent/JP2019519579A/ja active Pending
- 2017-06-30 WO PCT/KR2017/006980 patent/WO2018004306A1/en unknown
- 2017-06-30 RU RU2019102376A patent/RU2714206C1/ru active
-
2018
- 2018-11-27 PH PH12018502507A patent/PH12018502507A1/en unknown
- 2018-11-27 IL IL263306A patent/IL263306B/en active IP Right Grant
- 2018-11-28 SA SA518400547A patent/SA518400547B1/ar unknown
- 2018-11-28 SA SA521430937A patent/SA521430937B1/ar unknown
- 2018-12-07 CO CONC2018/0013293A patent/CO2018013293A2/es unknown
- 2018-12-07 CL CL2018003511A patent/CL2018003511A1/es unknown
- 2018-12-10 DO DO2018000275A patent/DOP2018000275A/es unknown
- 2018-12-13 ZA ZA2018/08431A patent/ZA201808431B/en unknown
- 2018-12-18 EC ECSENADI201893777A patent/ECSP18093777A/es unknown
-
2020
- 2020-06-04 JP JP2020097918A patent/JP7084961B2/ja active Active
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