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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- 0 *C(*)(C(*)(*)N(Cc1c2C(N)=O)C(N*)=O)[n]1nc2C1=CC2C(I)=C=C2C=C1 Chemical compound *C(*)(C(*)(*)N(Cc1c2C(N)=O)C(N*)=O)[n]1nc2C1=CC2C(I)=C=C2C=C1 0.000 description 23
- 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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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (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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Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016531020A Active 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 Active 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 Active 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) | ES2744636T3 (enExample) |
| TW (1) | TW201605859A (enExample) |
| UY (1) | UY35834A (enExample) |
| WO (2) | WO2015073767A1 (enExample) |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| JP6513075B2 (ja) * | 2014-02-27 | 2019-05-15 | 国立大学法人 東京大学 | オートタキシン阻害活性を有する縮合ピラゾール誘導体 |
| MA41338B1 (fr) * | 2015-01-16 | 2019-07-31 | Hoffmann La Roche | Composés de pyrazine pour le traitement de maladies infectieuses |
| CN109069488B (zh) | 2016-03-07 | 2021-09-07 | 英安塔制药有限公司 | 乙型肝炎抗病毒剂 |
| EP3426674A4 (en) | 2016-03-09 | 2019-08-14 | Blade Therapeutics, Inc. | CYCLIC KETO AMID COMPOUNDS AS CALPAIN MODULATORS AND METHOD FOR THE PRODUCTION AND USE THEREOF |
| CN109153682B (zh) * | 2016-05-20 | 2021-05-25 | 豪夫迈·罗氏有限公司 | 用于治疗感染性疾病的具有氧、硫和氮连接基的新的吡嗪化合物 |
| AU2017292646A1 (en) | 2016-07-05 | 2019-02-07 | Blade Therapeutics, Inc. | Calpain modulators and therapeutic uses thereof |
| EP3484886B1 (en) * | 2016-07-14 | 2020-03-04 | 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 |
| KR20190063473A (ko) | 2016-09-28 | 2019-06-07 | 블레이드 테라퓨틱스, 인크. | 칼페인 조정자 및 그 치료학적 용도 |
| 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 |
| CA3070004A1 (en) * | 2017-07-27 | 2019-01-31 | Jiangsu Hengrui Medicine Co., Ltd. | Piperazine heteroaryl derivative, preparation method therefor and use of same in medicine |
| TWI811236B (zh) | 2017-08-28 | 2023-08-11 | 美商因那塔製藥公司 | B型肝炎抗病毒試劑 |
| TWI846350B (zh) | 2017-09-15 | 2024-06-21 | 美商佛瑪治療公司 | 作為CBP/p300抑制劑之四氫-咪唑並喹啉化合物 |
| SG11202003827YA (en) | 2017-11-01 | 2020-05-28 | Bristol Myers Squibb Co | Bridged bicyclic compounds as farnesoid x receptor modulators |
| WO2019143902A2 (en) | 2018-01-22 | 2019-07-25 | Enanta Pharmaceuticals, Inc. | Substituted heterocycles as antiviral agents |
| WO2019191166A1 (en) * | 2018-03-29 | 2019-10-03 | Enanta Pharmaceuticals, Inc. | Hepatitis b antiviral agents |
| JP7090958B2 (ja) * | 2018-06-01 | 2022-06-27 | アドレイ・ノーティ・バイオファーマ・カンパニー・リミテッド | 高活性csf1r阻害薬化合物 |
| MX2023013508A (es) | 2018-06-29 | 2023-12-13 | Forma Therapeutics Inc | Inhibicion de la proteina de union a creb (cbp). |
| US10865211B2 (en) | 2018-09-21 | 2020-12-15 | Enanta Pharmaceuticals, Inc. | Functionalized heterocycles as antiviral agents |
| US11198693B2 (en) | 2018-11-21 | 2021-12-14 | Enanta Pharmaceuticals, Inc. | Functionalized heterocycles as antiviral agents |
| JP7608166B2 (ja) | 2019-01-11 | 2025-01-06 | 塩野義製薬株式会社 | Mgat2阻害活性を有するジヒドロピラゾロピラジノン誘導体 |
| 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 |
| BR112021014327A2 (pt) * | 2019-01-25 | 2021-09-28 | Jiangsu Hengrui Medicine Co., Ltd. | Forma cristalina de derivado de 1,2,3-triazolo[1,5-a]pirazinas, método de preparação da referida forma cristalina, composições farmacêuticas compreendendo a mesma e seu uso |
| 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 |
| CA3128946A1 (en) | 2019-02-07 | 2020-08-13 | 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) |
| US11236111B2 (en) | 2019-06-03 | 2022-02-01 | 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 |
| US11738019B2 (en) | 2019-07-11 | 2023-08-29 | Enanta Pharmaceuticals, Inc. | Substituted heterocycles as antiviral agents |
| US11236108B2 (en) | 2019-09-17 | 2022-02-01 | 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 |
| 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 |
| WO2022058920A1 (en) * | 2020-09-17 | 2022-03-24 | Janssen Pharmaceutica Nv | Casein kinase 1 delta modulators |
| 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 |
| TW202245772A (zh) * | 2021-02-04 | 2022-12-01 | 大陸商江蘇恆瑞醫藥股份有限公司 | 一種衣殼蛋白抑制劑的醫藥組成物及其製備方法 |
| EP4469457A1 (en) * | 2022-01-27 | 2024-12-04 | The Broad Institute Inc. | Substituted heterocyclic csnk1 inhibitors |
| CA3257905A1 (en) * | 2022-06-13 | 2025-04-24 | Shionogi & Co | CRYSTAL OF A DIHYDROPYRIDINONE DERIVATIVE OR A SOLVATE THEREOF |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2002337142B2 (en) * | 2001-09-19 | 2007-10-11 | Aventis Pharma S.A. | Indolizines as kinase protein inhibitors |
| JP4691506B2 (ja) * | 2003-12-11 | 2011-06-01 | アベンティス・ファーマスーティカルズ・インコーポレイテツド | カゼインキナーゼIεの阻害剤としての置換1H−ピロロ[3,2−b,3,2−c,及び2,3−c]ピリジン−2−カルボキシアミド及び関連類似物 |
| 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 |
| CA2738429C (en) | 2008-09-26 | 2016-10-25 | 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 |
| CA2826464C (en) | 2011-03-02 | 2020-07-28 | 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 |
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2014
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- 2014-11-13 AR ARP140104277A patent/AR098414A1/es unknown
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- 2014-11-14 WO PCT/US2014/065594 patent/WO2015073763A1/en not_active Ceased
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2016
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| UY35834A (es) | 2015-05-29 |
| EP3068785A1 (en) | 2016-09-21 |
| CN105916856A (zh) | 2016-08-31 |
| US20160311824A1 (en) | 2016-10-27 |
| CN105916855B (zh) | 2019-03-15 |
| US20150133428A1 (en) | 2015-05-14 |
| EP3068784B1 (en) | 2019-02-20 |
| CN105916856B (zh) | 2018-09-25 |
| WO2015073763A1 (en) | 2015-05-21 |
| US9273058B2 (en) | 2016-03-01 |
| JP6494624B2 (ja) | 2019-04-03 |
| CN105916855A (zh) | 2016-08-31 |
| TW201605859A (zh) | 2016-02-16 |
| JP2016537366A (ja) | 2016-12-01 |
| ES2744636T3 (es) | 2020-02-25 |
| JP2016537369A (ja) | 2016-12-01 |
| WO2015073767A1 (en) | 2015-05-21 |
| US9598423B2 (en) | 2017-03-21 |
| EP3068785B1 (en) | 2019-06-26 |
| US20160122358A1 (en) | 2016-05-05 |
| ES2718218T3 (es) | 2019-06-28 |
| AR098414A1 (es) | 2016-05-26 |
| EP3068784A1 (en) | 2016-09-21 |
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