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
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- 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 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) | US9273058B2 (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) | WO2015073763A1 (enExample) |
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|---|---|---|---|---|
| TW201605859A (zh) | 2013-11-14 | 2016-02-16 | 必治妥美雅史谷比公司 | 作為酪蛋白激酶1δ/ε抑制劑之新穎經取代之吡唑并-哌 |
| EP3112369A4 (en) * | 2014-02-27 | 2017-09-20 | 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 |
| 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 |
| WO2017198744A1 (en) * | 2016-05-20 | 2017-11-23 | 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 |
| WO2018064119A1 (en) | 2016-09-28 | 2018-04-05 | 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 |
| JP2020528062A (ja) * | 2017-07-27 | 2020-09-17 | 江蘇恒瑞医薬股▲ふん▼有限公司 | ピペラジンヘテロアリール誘導体、その製造方法、およびその医薬での使用 |
| SG11202001685TA (en) | 2017-08-28 | 2020-03-30 | Enanta Pharm Inc | Hepatitis b antiviral agents |
| TWI795440B (zh) | 2017-09-15 | 2023-03-11 | 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 |
| PE20201170A1 (es) | 2017-11-01 | 2020-10-28 | Bristol Myers Squibb Co | Compuestos biciclicos en puente como moduladores del receptor farnesoide x |
| US11058678B2 (en) | 2018-01-22 | 2021-07-13 | Enanta Pharmaceuticals, Inc. | Substituted heterocycles as antiviral agents |
| WO2019191166A1 (en) * | 2018-03-29 | 2019-10-03 | Enanta Pharmaceuticals, Inc. | Hepatitis b antiviral agents |
| WO2019228252A1 (zh) * | 2018-06-01 | 2019-12-05 | 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 |
| US10870648B2 (en) | 2018-06-29 | 2020-12-22 | Forma Therapeutics, Inc. | Inhibiting CREB binding protein (CBP) |
| JP2022500466A (ja) | 2018-09-21 | 2022-01-04 | エナンタ ファーマシューティカルズ インコーポレイテッド | 抗ウイルス剤としての官能化複素環 |
| IL283190B2 (en) | 2018-11-21 | 2025-08-01 | Enanta Pharm 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). |
| 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 |
| 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 |
| US20220081446A1 (en) * | 2019-01-25 | 2022-03-17 | Jiangsu Hengrui Medicine Co., Ltd. | Crystal form of 1,2,3-triazolo[1,5-a]pyrazines derivative and preparation method for crystal form |
| 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 |
| WO2020190791A1 (en) | 2019-03-15 | 2020-09-24 | Forma Therapeutics, Inc. | Inhibiting cyclic amp-responsive element-binding protein (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 |
| WO2020247575A1 (en) | 2019-06-04 | 2020-12-10 | Enanta Pharmaceuticals, Inc. | 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 |
| WO2021188414A1 (en) | 2020-03-16 | 2021-09-23 | Enanta Pharmaceuticals, Inc. | Functionalized heterocyclic compounds as antiviral agents |
| EP4188928B1 (en) | 2020-07-29 | 2024-07-24 | 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 |
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| 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 |
| EP4469457A4 (en) * | 2022-01-27 | 2026-01-21 | Broad Inst Inc | CSNK1 SUBSTITUTE HETEROCYCLIC INHIBITORS |
| KR20250022711A (ko) * | 2022-06-13 | 2025-02-17 | 시오노기 앤드 컴파니, 리미티드 | 다이하이드로피리딘온 유도체 또는 그 용매화물의 결정 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR0212760A (pt) * | 2001-09-19 | 2004-12-07 | Aventis Pharma Sa | Compostos quìmicos |
| ATE428711T1 (de) * | 2003-12-11 | 2009-05-15 | Aventis Pharma Inc | Substituierte 1h-pyrroloä3,2-b, 3,2-c und 2,3- cüpyridin-2-carbonsäureamide und verwandte analoga als inhibitoren von caseinkinase-i- epsilon |
| 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 |
| EP2346335B1 (en) | 2008-09-24 | 2018-11-14 | Basf Se | Pyrazole compounds for controlling invertebrate pests |
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2014
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| Publication number | Publication date |
|---|---|
| WO2015073763A1 (en) | 2015-05-21 |
| JP2016537369A (ja) | 2016-12-01 |
| CN105916855A (zh) | 2016-08-31 |
| US20160311824A1 (en) | 2016-10-27 |
| EP3068784A1 (en) | 2016-09-21 |
| TW201605859A (zh) | 2016-02-16 |
| ES2744636T3 (es) | 2020-02-25 |
| JP6494624B2 (ja) | 2019-04-03 |
| US9273058B2 (en) | 2016-03-01 |
| US20160122358A1 (en) | 2016-05-05 |
| WO2015073767A1 (en) | 2015-05-21 |
| US9598423B2 (en) | 2017-03-21 |
| EP3068784B1 (en) | 2019-02-20 |
| CN105916856B (zh) | 2018-09-25 |
| US20150133428A1 (en) | 2015-05-14 |
| AR098414A1 (es) | 2016-05-26 |
| ES2718218T3 (es) | 2019-06-28 |
| JP2016537366A (ja) | 2016-12-01 |
| UY35834A (es) | 2015-05-29 |
| CN105916855B (zh) | 2019-03-15 |
| CN105916856A (zh) | 2016-08-31 |
| EP3068785B1 (en) | 2019-06-26 |
| EP3068785A1 (en) | 2016-09-21 |
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