JP6494622B2 - カゼインキナーゼ1d/e阻害剤としての置換された4,5,6,7−テトラヒドロピラゾロ[1,5−a]ピラジン誘導体 - Google Patents
カゼインキナーゼ1d/e阻害剤としての置換された4,5,6,7−テトラヒドロピラゾロ[1,5−a]ピラジン誘導体 Download PDFInfo
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- JP6494622B2 JP6494622B2 JP2016531020A JP2016531020A JP6494622B2 JP 6494622 B2 JP6494622 B2 JP 6494622B2 JP 2016531020 A JP2016531020 A JP 2016531020A JP 2016531020 A JP2016531020 A JP 2016531020A JP 6494622 B2 JP6494622 B2 JP 6494622B2
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- XIYUDPFIVBAQIR-UHFFFAOYSA-N CC(C)(C)C(CNCc1c2C(N)=O)[n]1nc2-c(cc1)cc(Cl)c1F Chemical compound CC(C)(C)C(CNCc1c2C(N)=O)[n]1nc2-c(cc1)cc(Cl)c1F XIYUDPFIVBAQIR-UHFFFAOYSA-N 0.000 description 1
- XDYDVSBCFYDOGC-UHFFFAOYSA-N CC(C)(C)NC(N1Cc2c(C(N)=O)c(-c(cc3)ccc3F)n[n]2CC1)=O Chemical compound CC(C)(C)NC(N1Cc2c(C(N)=O)c(-c(cc3)ccc3F)n[n]2CC1)=O XDYDVSBCFYDOGC-UHFFFAOYSA-N 0.000 description 1
- HJEQFFNEOIFKNW-UHFFFAOYSA-N CC(C)(C)OC(N(CC(C1)(CC1(F)F)[n]1nc2-c(cc3Cl)ccc3F)Cc1c2C#N)=O Chemical compound CC(C)(C)OC(N(CC(C1)(CC1(F)F)[n]1nc2-c(cc3Cl)ccc3F)Cc1c2C#N)=O HJEQFFNEOIFKNW-UHFFFAOYSA-N 0.000 description 1
- VFSSJWVENCCWFU-UHFFFAOYSA-N CC(C)(C)OC(N1Cc2c(C(N)=O)c(-c(cc3Cl)ccc3F)n[n]2C(C2)(CN2C(C)=O)C1)=O Chemical compound CC(C)(C)OC(N1Cc2c(C(N)=O)c(-c(cc3Cl)ccc3F)n[n]2C(C2)(CN2C(C)=O)C1)=O VFSSJWVENCCWFU-UHFFFAOYSA-N 0.000 description 1
- UVTPQTJCMDNPNF-UHFFFAOYSA-N CC(N(C1)CC1(CN(Cc1c2C(N)=O)C(Nc(cc3)ccc3C#N)=O)[n]1nc2-c(cc1Cl)ccc1F)=O Chemical compound CC(N(C1)CC1(CN(Cc1c2C(N)=O)C(Nc(cc3)ccc3C#N)=O)[n]1nc2-c(cc1Cl)ccc1F)=O UVTPQTJCMDNPNF-UHFFFAOYSA-N 0.000 description 1
- GRHSKAJSDPCSGJ-UHFFFAOYSA-N CC(c(cc1)ccc1NC(N1Cc2c(C(NC)=O)c(-c(cc3Cl)ccc3F)n[n]2CC1)=O)=N Chemical compound CC(c(cc1)ccc1NC(N1Cc2c(C(NC)=O)c(-c(cc3Cl)ccc3F)n[n]2CC1)=O)=N GRHSKAJSDPCSGJ-UHFFFAOYSA-N 0.000 description 1
- BPEHMUFZONYKGS-UHFFFAOYSA-N CC1=NN(C)C2C(C)=CC(SC)=CC12 Chemical compound CC1=NN(C)C2C(C)=CC(SC)=CC12 BPEHMUFZONYKGS-UHFFFAOYSA-N 0.000 description 1
- YZSRXZDCFJKCCC-UHFFFAOYSA-N CCC(CN(Cc1c2C(N)=O)C(Nc3ccc(C=N)cc3)=O)[n]1nc2-c(cc1Cl)ccc1F Chemical compound CCC(CN(Cc1c2C(N)=O)C(Nc3ccc(C=N)cc3)=O)[n]1nc2-c(cc1Cl)ccc1F YZSRXZDCFJKCCC-UHFFFAOYSA-N 0.000 description 1
- UEITWDSZSRMKGJ-UHFFFAOYSA-O CCC[NH2+]C(C(N)=O)=CC(c1cccc(F)c1)N Chemical compound CCC[NH2+]C(C(N)=O)=CC(c1cccc(F)c1)N UEITWDSZSRMKGJ-UHFFFAOYSA-O 0.000 description 1
- XOJUHLHQTCZSCT-UHFFFAOYSA-N CCOC(c1cc(-c2cccc(Cl)c2)n[nH]1)=O Chemical compound CCOC(c1cc(-c2cccc(Cl)c2)n[nH]1)=O XOJUHLHQTCZSCT-UHFFFAOYSA-N 0.000 description 1
- YYMKFRVJUIODKY-UHFFFAOYSA-N Cc(c1c2)n[n](C)c1c(C)cc2-c1n[n](CCNC2)c2c1C(N)=O Chemical compound Cc(c1c2)n[n](C)c1c(C)cc2-c1n[n](CCNC2)c2c1C(N)=O YYMKFRVJUIODKY-UHFFFAOYSA-N 0.000 description 1
- SVNWADDAMRRSMC-UHFFFAOYSA-N Cc1cc(-c2n[n](CCNC3)c3c2C(N)=O)ccc1F Chemical compound Cc1cc(-c2n[n](CCNC3)c3c2C(N)=O)ccc1F SVNWADDAMRRSMC-UHFFFAOYSA-N 0.000 description 1
- FZDRIFGHXKAKDA-UHFFFAOYSA-O N=C(C=C1[NH2+]C(C2)(CC2(F)F)CN=C1)c(cc1Cl)ccc1F Chemical compound N=C(C=C1[NH2+]C(C2)(CC2(F)F)CN=C1)c(cc1Cl)ccc1F FZDRIFGHXKAKDA-UHFFFAOYSA-O 0.000 description 1
- HXBBQZYKGKTURA-UHFFFAOYSA-N NC(c1c(CN(CC2)C(Nc(cc3)ccc3C#N)=O)[n]2nc1-c(cc1Cl)c[n]2c1cnc2)=O Chemical compound NC(c1c(CN(CC2)C(Nc(cc3)ccc3C#N)=O)[n]2nc1-c(cc1Cl)c[n]2c1cnc2)=O HXBBQZYKGKTURA-UHFFFAOYSA-N 0.000 description 1
- CKKVLWJJPHNJEU-UHFFFAOYSA-N NC(c1c(CN(CC23COC2)C(Nc(cc2)ccc2C#N)=O)[n]3nc1-c(cc1Cl)ccc1F)=O Chemical compound NC(c1c(CN(CC23COC2)C(Nc(cc2)ccc2C#N)=O)[n]3nc1-c(cc1Cl)ccc1F)=O CKKVLWJJPHNJEU-UHFFFAOYSA-N 0.000 description 1
- JUFQRDRSSPZIQS-UHFFFAOYSA-N NC(c1c(CNC2(CC2)C2)[n]2nc1-c(cc1Cl)ccc1F)=O Chemical compound NC(c1c(CNC2(CC2)C2)[n]2nc1-c(cc1Cl)ccc1F)=O JUFQRDRSSPZIQS-UHFFFAOYSA-N 0.000 description 1
- LNFJKWTWLJASLK-UHFFFAOYSA-N NC(c1c(CNCC2)[n]2nc1-c1cc([nH]nc2)c2c(F)c1)=O Chemical compound NC(c1c(CNCC2)[n]2nc1-c1cc([nH]nc2)c2c(F)c1)=O LNFJKWTWLJASLK-UHFFFAOYSA-N 0.000 description 1
- LKKMZEYUOUHKGH-UHFFFAOYSA-N NC(c1c(CNCC2CF)[n]2nc1-c(cc1Cl)ccc1Cl)=O Chemical compound NC(c1c(CNCC2CF)[n]2nc1-c(cc1Cl)ccc1Cl)=O LKKMZEYUOUHKGH-UHFFFAOYSA-N 0.000 description 1
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
- 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
- A61P25/00—Drugs for disorders of the nervous 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
- 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
- C07D487/10—Spiro-condensed systems
-
- 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
- C07D487/12—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 three hetero rings
- C07D487/20—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
- C07D491/14—Ortho-condensed systems
- C07D491/147—Ortho-condensed systems the condensed system containing one ring with oxygen as ring hetero atom and two rings with nitrogen as ring hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
- C07D491/20—Spiro-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
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurosurgery (AREA)
- Oncology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Hematology (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361904116P | 2013-11-14 | 2013-11-14 | |
| US61/904,116 | 2013-11-14 | ||
| PCT/US2014/065599 WO2015073767A1 (en) | 2013-11-14 | 2014-11-14 | Substituted 4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine derivatives as casein kinase 1 d/e inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016537366A JP2016537366A (ja) | 2016-12-01 |
| JP2016537366A5 JP2016537366A5 (enExample) | 2017-12-21 |
| JP6494622B2 true JP6494622B2 (ja) | 2019-04-03 |
Family
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016531020A Expired - Fee Related JP6494622B2 (ja) | 2013-11-14 | 2014-11-14 | カゼインキナーゼ1d/e阻害剤としての置換された4,5,6,7−テトラヒドロピラゾロ[1,5−a]ピラジン誘導体 |
| JP2016531646A Expired - Fee Related JP6494624B2 (ja) | 2013-11-14 | 2014-11-14 | カゼインキナーゼ1d/e阻害剤としての置換された4,5,6,7−テトラヒドロピラゾロ[1,5−a]ピラジン誘導体 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
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| JP2016531646A Expired - Fee Related JP6494624B2 (ja) | 2013-11-14 | 2014-11-14 | カゼインキナーゼ1d/e阻害剤としての置換された4,5,6,7−テトラヒドロピラゾロ[1,5−a]ピラジン誘導体 |
Country Status (9)
| Country | Link |
|---|---|
| US (3) | US9598423B2 (enExample) |
| EP (2) | EP3068784B1 (enExample) |
| JP (2) | JP6494622B2 (enExample) |
| CN (2) | CN105916855B (enExample) |
| AR (1) | AR098414A1 (enExample) |
| ES (2) | ES2718218T3 (enExample) |
| TW (1) | TW201605859A (enExample) |
| UY (1) | UY35834A (enExample) |
| WO (2) | WO2015073767A1 (enExample) |
Families Citing this family (41)
| Publication number | Priority date | Publication date | Assignee | Title |
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| UY35834A (es) | 2013-11-14 | 2015-05-29 | Bristol Myers Squibb Company Una Corporación Del Estado De Delaware | Piperazinas de pirazolo sustituido como inhibidores de caseína quinasa 1 delta y epsilon |
| US10189843B2 (en) | 2014-02-27 | 2019-01-29 | The University Of Tokyo | Fused pyrazole derivative having autotaxin inhibitory activity |
| MA41338B1 (fr) * | 2015-01-16 | 2019-07-31 | Hoffmann La Roche | Composés de pyrazine pour le traitement de maladies infectieuses |
| KR102398439B1 (ko) | 2016-03-07 | 2022-05-16 | 이난타 파마슈티칼스, 인코포레이티드 | B형 간염 항바이러스제 |
| WO2017156071A1 (en) | 2016-03-09 | 2017-09-14 | Blade Therapeutics, Inc. | Cyclic keto-amide compounds as calpain modulators and methods of production and use thereof |
| EP3458455B1 (en) * | 2016-05-20 | 2021-06-16 | F. Hoffmann-La Roche AG | Novel pyrazine compounds with oxygen, sulfur and nitrogen linker for the treatment of infectious diseases |
| AU2017292646A1 (en) | 2016-07-05 | 2019-02-07 | Blade Therapeutics, Inc. | Calpain modulators and therapeutic uses thereof |
| WO2018011163A1 (en) * | 2016-07-14 | 2018-01-18 | F. Hoffmann-La Roche Ag | 6,7-dihydro-4h-pyrazolo[1,5-a]pyrazine and 6,7-dihydro-4h-triazolo[1,5-a]pyrazine compounds for the treatment of infectious diseases |
| US10934261B2 (en) | 2016-09-28 | 2021-03-02 | Blade Therapeutics, Inc. | Calpain modulators and therapeutic uses thereof |
| TWI782056B (zh) | 2017-07-14 | 2022-11-01 | 日商鹽野義製藥股份有限公司 | 具有mgat2抑制活性的縮合環衍生物 |
| KR20200032702A (ko) * | 2017-07-27 | 2020-03-26 | 지앙수 헨그루이 메디슨 컴퍼니 리미티드 | 피페라진 헤테로아릴 유도체, 그 제조 방법 및 의약에서 이의 용도 |
| SG11202001685TA (en) | 2017-08-28 | 2020-03-30 | Enanta Pharm Inc | Hepatitis b antiviral agents |
| WO2019055877A1 (en) | 2017-09-15 | 2019-03-21 | Forma Therapeutics, Inc. | TETRAHYDROIMIDAZO QUINOLINE COMPOSITIONS AS INHIBITORS OF CBP / P300 |
| JP7212693B2 (ja) | 2017-11-01 | 2023-01-25 | ブリストル-マイヤーズ スクイブ カンパニー | ファルネソイドx受容体モジュレーターとしての架橋二環化合物 |
| US11058678B2 (en) | 2018-01-22 | 2021-07-13 | Enanta Pharmaceuticals, Inc. | Substituted heterocycles as antiviral agents |
| US10729688B2 (en) * | 2018-03-29 | 2020-08-04 | Enanta Pharmaceuticals, Inc. | Hepatitis B antiviral agents |
| CN111295380B (zh) * | 2018-06-01 | 2020-11-20 | 杭州阿诺生物医药科技有限公司 | 一种高活性csf1r抑制剂化合物 |
| IL279734B2 (en) | 2018-06-29 | 2024-11-01 | Forma Therapeutics Inc | Inhibiting creb binding protein (cbp) |
| TW202024093A (zh) | 2018-09-21 | 2020-07-01 | 美商安塔製藥公司 | 作為抗病毒劑之官能化雜環 |
| EP3883570A4 (en) | 2018-11-21 | 2022-07-13 | Enanta Pharmaceuticals, Inc. | FUNCTIONALIZED HETEROCYCLES AS ANTIVIRAL AGENTS |
| MX2021008050A (es) | 2019-01-11 | 2021-08-05 | Shionogi & Co | Derivado de dihidropirazolopirazinona que tiene actividad inhibidora de monoacilglicerol aciltransferasa 2 (mgat2). |
| CN111484497B (zh) * | 2019-01-25 | 2021-07-02 | 江苏恒瑞医药股份有限公司 | 咪唑并[1,5-a]吡嗪类衍生物的可药用盐、晶型及其制备方法 |
| CN111484498B (zh) * | 2019-01-25 | 2021-05-14 | 江苏恒瑞医药股份有限公司 | 咪唑并[1,5-a]吡嗪类化合物的晶型及其制备方法 |
| MX2021008929A (es) * | 2019-01-25 | 2021-08-24 | Jiangsu Hengrui Medicine Co | Forma cristalina de un derivado de 1,2,3-triazolo[1,5-a]pirazinas, y metodo de preparacion para la forma de cristal. |
| EP3921317B1 (en) | 2019-02-07 | 2023-08-02 | Bayer Aktiengesellschaft | 3-amino-2-[2-(acylamino)pyridin-4-yl]-1,5,6,7-tetrahydro-4h-pyrrolo[3,2-c]pyridin-4-one as csnk1 inhibitors |
| TW202102494A (zh) | 2019-03-15 | 2021-01-16 | 美商弗瑪治療公司 | 抑制環amp-反應元件-結合蛋白(creb) |
| WO2020247444A1 (en) | 2019-06-03 | 2020-12-10 | Enanta Pharmaceuticals, Inc, | Hepatitis b antiviral agents |
| WO2020247561A1 (en) | 2019-06-04 | 2020-12-10 | Enanta Pharmaceuticals, Inc, | Hepatitis b antiviral agents |
| US11472808B2 (en) | 2019-06-04 | 2022-10-18 | Enanta Pharmaceuticals, Inc. | Substituted pyrrolo[1,2-c]pyrimidines as hepatitis B antiviral agents |
| WO2021007488A1 (en) | 2019-07-11 | 2021-01-14 | Enanta Pharmaceuticals, Inc. | Substituted heterocycles as antiviral agents |
| WO2021055425A2 (en) | 2019-09-17 | 2021-03-25 | Enanta Pharmaceuticals, Inc. | Functionalized heterocycles as antiviral agents |
| US11802125B2 (en) | 2020-03-16 | 2023-10-31 | Enanta Pharmaceuticals, Inc. | Functionalized heterocyclic compounds as antiviral agents |
| WO2022023340A1 (en) | 2020-07-29 | 2022-02-03 | Bayer Aktiengesellschaft | Substituted heterocyclic compounds and therapeutic uses thereof |
| WO2022023341A1 (en) | 2020-07-29 | 2022-02-03 | Bayer Aktiengesellschaft | Substituted 1 h-pyrrolo[3,2-b]pyridin compounds and methods of use thereof |
| CN114057745A (zh) * | 2020-07-29 | 2022-02-18 | 江苏恒瑞医药股份有限公司 | 一种三氮唑并[1,5-a]吡嗪制备方法及其应用 |
| JP2023541465A (ja) * | 2020-09-17 | 2023-10-02 | ヤンセン ファーマシューティカ エヌ.ベー. | カゼインキナーゼ1デルタモジュレーター |
| US11795168B2 (en) | 2020-09-23 | 2023-10-24 | Forma Therapeutics, Inc. | Inhibiting cyclic amp-responsive element-binding protein (CREB) binding protein (CBP) |
| US11801243B2 (en) | 2020-09-23 | 2023-10-31 | Forma Therapeutics, Inc. | Bromodomain inhibitors for androgen receptor-driven cancers |
| WO2022166778A1 (zh) * | 2021-02-04 | 2022-08-11 | 江苏恒瑞医药股份有限公司 | 一种衣壳蛋白抑制剂的药物组合物及其制备方法 |
| US20250188075A1 (en) * | 2022-01-27 | 2025-06-12 | The Broad Institute, Inc. | Substituted heterocyclic csnk1 inhibitors |
| CA3257905A1 (en) * | 2022-06-13 | 2025-04-24 | Shionogi & Co., Ltd. | CRYSTAL OF A DIHYDROPYRIDINONE DERIVATIVE OR A SOLVATE THEREOF |
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|---|---|---|---|---|
| CN100391958C (zh) * | 2001-09-19 | 2008-06-04 | 安万特医药股份有限公司 | 化合物 |
| CN100439367C (zh) * | 2003-12-11 | 2008-12-03 | 安万特药物公司 | 作为酪蛋白激酶Iε抑制剂的取代的1H-吡咯并[3,2-b、3,2-c和2,3-c]吡啶-2-甲酰胺以及相关类似物 |
| US20050222171A1 (en) * | 2004-01-22 | 2005-10-06 | Guido Bold | Organic compounds |
| US20070155738A1 (en) | 2005-05-20 | 2007-07-05 | Alantos Pharmaceuticals, Inc. | Heterobicyclic metalloprotease inhibitors |
| CN101417999A (zh) | 2007-10-25 | 2009-04-29 | 上海恒瑞医药有限公司 | 哌嗪类衍生物,其制备方法及其在医药上的应用 |
| EP2085398A1 (en) | 2008-02-01 | 2009-08-05 | Merz Pharma GmbH & Co. KGaA | Pyrazolopyrimidines, a process for their preparation and their use as medicine |
| ES2710701T3 (es) | 2008-09-24 | 2019-04-26 | Basf Se | Compuestos de pirazol para el control de plagas de invertebrados |
| WO2010036380A1 (en) | 2008-09-26 | 2010-04-01 | Intellikine, Inc. | Heterocyclic kinase inhibitors |
| WO2010059836A1 (en) | 2008-11-20 | 2010-05-27 | Decode Genetics Ehf | Substituted aza-bridged bicyclics for cardiovascular and cns disease |
| TW201035102A (en) | 2009-03-04 | 2010-10-01 | Gruenethal Gmbh | Sulfonylated tetrahydroazolopyrazines and their use as medicinal products |
| FR2960876B1 (fr) * | 2010-06-03 | 2012-07-27 | Sanofi Aventis | Derives de 3,4-dihydropyrrolo[1,2-a]pyrazine-2,8(1h)-dicarboxamide leur preparation et leur application en therapeutique. |
| CN102372716A (zh) | 2010-08-09 | 2012-03-14 | 江苏恒瑞医药股份有限公司 | 酞嗪酮类衍生物、其制备方法及其在医药上的应用 |
| WO2012117048A1 (en) | 2011-03-02 | 2012-09-07 | Lead Discovery Center Gmbh | Pharmaceutically active disubstituted triazine derivatives |
| UY35834A (es) | 2013-11-14 | 2015-05-29 | Bristol Myers Squibb Company Una Corporación Del Estado De Delaware | Piperazinas de pirazolo sustituido como inhibidores de caseína quinasa 1 delta y epsilon |
-
2014
- 2014-11-13 UY UY0001035834A patent/UY35834A/es unknown
- 2014-11-13 AR ARP140104277A patent/AR098414A1/es unknown
- 2014-11-13 TW TW103139448A patent/TW201605859A/zh unknown
- 2014-11-14 EP EP14802796.4A patent/EP3068784B1/en not_active Not-in-force
- 2014-11-14 CN CN201480073088.8A patent/CN105916855B/zh not_active Expired - Fee Related
- 2014-11-14 ES ES14802796T patent/ES2718218T3/es active Active
- 2014-11-14 US US15/034,217 patent/US9598423B2/en active Active
- 2014-11-14 ES ES14806145T patent/ES2744636T3/es active Active
- 2014-11-14 WO PCT/US2014/065599 patent/WO2015073767A1/en not_active Ceased
- 2014-11-14 JP JP2016531020A patent/JP6494622B2/ja not_active Expired - Fee Related
- 2014-11-14 CN CN201480073199.9A patent/CN105916856B/zh not_active Expired - Fee Related
- 2014-11-14 EP EP14806145.0A patent/EP3068785B1/en not_active Not-in-force
- 2014-11-14 JP JP2016531646A patent/JP6494624B2/ja not_active Expired - Fee Related
- 2014-11-14 US US14/541,343 patent/US9273058B2/en active Active
- 2014-11-14 WO PCT/US2014/065594 patent/WO2015073763A1/en not_active Ceased
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2016
- 2016-01-13 US US14/994,346 patent/US20160122358A1/en not_active Abandoned
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| US20150133428A1 (en) | 2015-05-14 |
| CN105916856A (zh) | 2016-08-31 |
| ES2744636T3 (es) | 2020-02-25 |
| EP3068784A1 (en) | 2016-09-21 |
| EP3068784B1 (en) | 2019-02-20 |
| WO2015073767A1 (en) | 2015-05-21 |
| JP6494624B2 (ja) | 2019-04-03 |
| EP3068785A1 (en) | 2016-09-21 |
| US9273058B2 (en) | 2016-03-01 |
| US20160122358A1 (en) | 2016-05-05 |
| ES2718218T3 (es) | 2019-06-28 |
| JP2016537369A (ja) | 2016-12-01 |
| AR098414A1 (es) | 2016-05-26 |
| UY35834A (es) | 2015-05-29 |
| CN105916855A (zh) | 2016-08-31 |
| CN105916855B (zh) | 2019-03-15 |
| CN105916856B (zh) | 2018-09-25 |
| US9598423B2 (en) | 2017-03-21 |
| JP2016537366A (ja) | 2016-12-01 |
| WO2015073763A1 (en) | 2015-05-21 |
| TW201605859A (zh) | 2016-02-16 |
| US20160311824A1 (en) | 2016-10-27 |
| EP3068785B1 (en) | 2019-06-26 |
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