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
- OGEBRHQLRGFBNV-RZDIXWSQSA-N chembl2036808 Chemical class C12=NC(NCCCC)=NC=C2C(C=2C=CC(F)=CC=2)=NN1C[C@H]1CC[C@H](N)CC1 OGEBRHQLRGFBNV-RZDIXWSQSA-N 0.000 title abstract 2
- 229940043355 kinase inhibitor Drugs 0.000 title abstract 2
- 239000003757 phosphotransferase inhibitor Substances 0.000 title abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 108091000080 Phosphotransferase Proteins 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 230000008520 organization Effects 0.000 abstract 1
- 102000020233 phosphotransferase Human genes 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Transplantation (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR20160083050 | 2016-06-30 | ||
| PCT/KR2017/006980 WO2018004306A1 (fr) | 2016-06-30 | 2017-06-30 | Dérivés de pyrazolopyrimidine comme inhibiteurs de kinase |
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 (23)
| Country | Link |
|---|---|
| US (1) | US10961247B2 (fr) |
| EP (2) | EP3950691A1 (fr) |
| JP (2) | JP2019519579A (fr) |
| KR (1) | KR102329162B1 (fr) |
| CN (2) | CN113135920A (fr) |
| AU (1) | AU2017287762C1 (fr) |
| BR (1) | BR112018074621B1 (fr) |
| CA (1) | CA3025636C (fr) |
| CL (1) | CL2018003511A1 (fr) |
| CO (1) | CO2018013293A2 (fr) |
| DO (1) | DOP2018000275A (fr) |
| EC (1) | ECSP18093777A (fr) |
| ES (1) | ES2977557T3 (fr) |
| IL (1) | IL263306B (fr) |
| MX (2) | MX2018016287A (fr) |
| MY (1) | MY191110A (fr) |
| PE (1) | PE20190811A1 (fr) |
| PH (1) | PH12018502507A1 (fr) |
| RU (1) | RU2714206C1 (fr) |
| SA (2) | SA521430937B1 (fr) |
| SG (1) | SG11201811470PA (fr) |
| WO (1) | WO2018004306A1 (fr) |
| ZA (1) | ZA201808431B (fr) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| UA125318C2 (uk) | 2017-08-01 | 2022-02-16 | Тереванс Байофарма Ар Енд Ді Айпі, Елелсі | Піразоло- і триазолобіциклічні сполуки як інгібітори jak-кінази |
| SI3733673T1 (sl) * | 2017-12-28 | 2022-09-30 | Daewoong Pharmaceutical Co., Ltd. | Oksi-fluoropiperidinski derivat kot kinazni inhibitor |
| 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 (fr) | 2018-08-10 | 2022-05-18 | Aclaris Therapeutics, Inc. | Inhibiteurs de pyrrolopyrimidine itk |
| CA3125039A1 (fr) | 2019-01-23 | 2020-07-30 | Theravance Biopharma R&D Ip, Llc | Imidazo[1,5-a]pyridine,1,2,4-triazolo[4,3-a]pyridine et imidazo[1,5-a]pyrazine utilisees en tant qu'inhibiteurs de jak |
| US20210395247A1 (en) * | 2019-03-18 | 2021-12-23 | Shanghai Haiyan Pharmaceutical Technology Co., Ltd. | Btk inhibitors, pharmaceutically acceptable salts, polymorphs and application thereof |
| 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 |
| 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 |
| WO2021147953A1 (fr) * | 2020-01-21 | 2021-07-29 | 江苏先声药业有限公司 | Dérivé cyclique pyrimidino à cinq chaînons et application correspondante |
| WO2021147952A1 (fr) * | 2020-01-21 | 2021-07-29 | 江苏先声药业有限公司 | Composé pyrimidopyrrole |
| 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 |
| 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 |
| WO2022002118A1 (fr) * | 2020-07-01 | 2022-01-06 | 四川海思科制药有限公司 | Dérivé hétérocyclique à cycles fusionnés et son utilisation médicale |
| 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 |
| WO2022140246A1 (fr) | 2020-12-21 | 2022-06-30 | Hangzhou Jijing Pharmaceutical Technology Limited | Procédés et composés destinés à l'autophagie ciblée |
| WO2023242597A1 (fr) * | 2022-06-16 | 2023-12-21 | Amphista Therapeutics Limited | Molécules bifonctionnelles pour la dégradation ciblée de protéines |
| 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 |
| MXPA04009243A (es) * | 2002-04-12 | 2005-06-08 | Pfizer | Uso de ligandos para el receptor ep4 en el tratamiento de enfermedades vinculadas a il-6. |
| US8163767B2 (en) | 2005-07-14 | 2012-04-24 | Astellas Pharma Inc. | Heterocyclic Janus Kinase 3 inhibitors |
| UA116187C2 (uk) | 2005-12-13 | 2018-02-26 | Інсайт Холдінгс Корпорейшн | ГЕТЕРОАРИЛЗАМІЩЕНІ ПІРОЛО[2,3-b]ПІРИДИНИ Й ПІРОЛО[2,3-b]ПІРИМІДИНИ ЯК ІНГІБІТОРИ ЯНУС-КІНАЗИ |
| EP2532235A1 (fr) | 2006-09-22 | 2012-12-12 | Pharmacyclics, Inc. | Inhibiteurs de la tyrosine kinase de bruton |
| EP2170830B1 (fr) | 2007-07-17 | 2014-10-15 | Plexxikon, Inc. | COMPOSÉS DE 2-FLUORO-BENZÈNESULFONAMIDE COMME MODULATEURS DE LA KINASE Raf |
| WO2009026107A1 (fr) * | 2007-08-17 | 2009-02-26 | Portola Pharmaceuticals, Inc. | Inhibiteurs de protéine kinases |
| JP2011500806A (ja) | 2007-10-25 | 2011-01-06 | メルク・シャープ・エンド・ドーム・コーポレイション | 治療用化合物 |
| JP2011518219A (ja) | 2008-04-22 | 2011-06-23 | ポートラ ファーマシューティカルズ， インコーポレイテッド | タンパク質キナーゼの阻害剤 |
| PE20091846A1 (es) * | 2008-05-19 | 2009-12-16 | Plexxikon Inc | DERIVADOS DE PIRROLO[2,3-d]-PIRIMIDINA COMO MODULADORES DE CINASAS |
| MX2011000661A (es) | 2008-07-16 | 2011-05-25 | Pharmacyclics Inc | Inhibidores de tirosina cinasa de bruton para el tratamiento de tumores solidos. |
| CA2760794C (fr) * | 2009-05-05 | 2017-07-25 | Dana Farber Cancer Institute | Inhibiteurs d'egfr et procedes de traitement de troubles |
| CN102711470A (zh) | 2009-12-01 | 2012-10-03 | 雅培制药有限公司 | 新的三环化合物 |
| LT2975042T (lt) * | 2010-06-23 | 2019-01-25 | Hanmi Science Co., Ltd. | Naujieji kondensuoti pirimidino dariniai, skirti tirozino kinazės aktyvumo slopinimui |
| JP6014149B2 (ja) | 2011-09-22 | 2016-10-25 | メルク・シャープ・アンド・ドーム・コーポレーションＭｅｒｃｋ Ｓｈａｒｐ ＆ Ｄｏｈｍｅ Ｃｏｒｐ． | ヤヌスキナーゼ阻害剤としての非環式シアノエチルピラゾール |
| US20150166591A1 (en) * | 2012-05-05 | 2015-06-18 | Ariad Pharmaceuticals, Inc. | Methods and compositions for raf kinase mediated diseases |
| US9469644B2 (en) | 2013-03-05 | 2016-10-18 | Hoffmann-La Roche Inc. | Inhibitors of Bruton's tyrosine kinase |
| CN105916851A (zh) | 2013-07-11 | 2016-08-31 | 艾森生物科学公司 | 嘧啶衍生物作为激酶抑制剂 |
| CN104311573B (zh) | 2013-09-18 | 2017-12-15 | 北京韩美药品有限公司 | 抑制btk和/或jak3激酶活性的化合物 |
| TN2016000227A1 (fr) * | 2013-12-05 | 2017-10-06 | Pfizer | Pyrrolo[2,3-d]pyrimidinyle, pyrrolo[2,3-b]pyrazinyle et pyrollo[2,3-d]pyridinyle acrylamides. |
| CN105777756B (zh) * | 2014-07-02 | 2019-03-01 | 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 |
| 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 |
| WO2016130920A2 (fr) | 2015-02-13 | 2016-08-18 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de lrrk2 et leurs méthodes de production et d'utilisation |
-
2017
- 2017-06-30 US US16/304,798 patent/US10961247B2/en active Active
- 2017-06-30 AU AU2017287762A patent/AU2017287762C1/en active Active
- 2017-06-30 KR KR1020170083259A patent/KR102329162B1/ko active IP Right Grant
- 2017-06-30 PE PE2018003174A patent/PE20190811A1/es unknown
- 2017-06-30 EP EP21190933.8A patent/EP3950691A1/fr active Pending
- 2017-06-30 MX MX2018016287A patent/MX2018016287A/es unknown
- 2017-06-30 BR BR112018074621-5A patent/BR112018074621B1/pt active IP Right Grant
- 2017-06-30 SG SG11201811470PA patent/SG11201811470PA/en unknown
- 2017-06-30 RU RU2019102376A patent/RU2714206C1/ru active
- 2017-06-30 CA CA3025636A patent/CA3025636C/fr active Active
- 2017-06-30 CN CN202110351304.2A patent/CN113135920A/zh active Pending
- 2017-06-30 MY MYPI2018002167A patent/MY191110A/en unknown
- 2017-06-30 JP JP2018568407A patent/JP2019519579A/ja active Pending
- 2017-06-30 CN CN201780039336.0A patent/CN109311896B/zh active Active
- 2017-06-30 MX MX2021009378A patent/MX2021009378A/es unknown
- 2017-06-30 WO PCT/KR2017/006980 patent/WO2018004306A1/fr unknown
- 2017-06-30 EP EP17820582.9A patent/EP3478687B1/fr active Active
- 2017-06-30 ES ES17820582T patent/ES2977557T3/es active Active
-
2018
- 2018-11-27 IL IL263306A patent/IL263306B/en active IP Right Grant
- 2018-11-27 PH PH12018502507A patent/PH12018502507A1/en unknown
- 2018-11-28 SA SA521430937A patent/SA521430937B1/ar unknown
- 2018-11-28 SA SA518400547A patent/SA518400547B1/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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