JP6820097B2 - 脂質合成の複素環式モジュレータ及びその組み合わせ - Google Patents
脂質合成の複素環式モジュレータ及びその組み合わせ Download PDFInfo
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- JP6820097B2 JP6820097B2 JP2016541077A JP2016541077A JP6820097B2 JP 6820097 B2 JP6820097 B2 JP 6820097B2 JP 2016541077 A JP2016541077 A JP 2016541077A JP 2016541077 A JP2016541077 A JP 2016541077A JP 6820097 B2 JP6820097 B2 JP 6820097B2
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- BRXURDRHDWBVCB-UHFFFAOYSA-N CC(C)N(CC1)CCc2c1[nH]c(-c1cc(C(OC)=O)c(C)cc1C)n2 Chemical compound CC(C)N(CC1)CCc2c1[nH]c(-c1cc(C(OC)=O)c(C)cc1C)n2 BRXURDRHDWBVCB-UHFFFAOYSA-N 0.000 description 2
- ZDIRWELLEJKATA-UHFFFAOYSA-N Cc1ncc(-c(cc(cc2)C(N(CC3)CCC3c(cc3)ccc3C#N)=O)c2F)[nH]1 Chemical compound Cc1ncc(-c(cc(cc2)C(N(CC3)CCC3c(cc3)ccc3C#N)=O)c2F)[nH]1 ZDIRWELLEJKATA-UHFFFAOYSA-N 0.000 description 2
- TVLGRZQCWCXWLY-UHFFFAOYSA-N CCNC(c1cc(-c2nc(CCN(CC3)C(C)C)c3[nH]2)c(C)cc1C)=O Chemical compound CCNC(c1cc(-c2nc(CCN(CC3)C(C)C)c3[nH]2)c(C)cc1C)=O TVLGRZQCWCXWLY-UHFFFAOYSA-N 0.000 description 1
- MJYBXPWMRJYBGF-UHFFFAOYSA-N COC(c(cc1)cc(C(CBr)=O)c1F)=O Chemical compound COC(c(cc1)cc(C(CBr)=O)c1F)=O MJYBXPWMRJYBGF-UHFFFAOYSA-N 0.000 description 1
- TVWIPEIGOLZWKK-UHFFFAOYSA-N Cc(c(C(N(C1)CC1c(cc1)ccc1C#N)=O)c1)cc(C)c1-c1nc(CCN(C)CC2)c2[nH]1 Chemical compound Cc(c(C(N(C1)CC1c(cc1)ccc1C#N)=O)c1)cc(C)c1-c1nc(CCN(C)CC2)c2[nH]1 TVWIPEIGOLZWKK-UHFFFAOYSA-N 0.000 description 1
- DRYJZAQMCNFRHK-UHFFFAOYSA-N Cc(c(C(N(C1)CC1c(cc1)ccc1C#N)=O)c1)cc(C)c1-c1nc2cc(N3CCCC3)ncc2[nH]1 Chemical compound Cc(c(C(N(C1)CC1c(cc1)ccc1C#N)=O)c1)cc(C)c1-c1nc2cc(N3CCCC3)ncc2[nH]1 DRYJZAQMCNFRHK-UHFFFAOYSA-N 0.000 description 1
- XJOGNWALXQXHCN-UHFFFAOYSA-N Cc(ccc(C(N(C1)CC1c(cc1)ccc1C#N)=O)c1)c1-c1nc2cc(N3CCC3)ncc2[nH]1 Chemical compound Cc(ccc(C(N(C1)CC1c(cc1)ccc1C#N)=O)c1)c1-c1nc2cc(N3CCC3)ncc2[nH]1 XJOGNWALXQXHCN-UHFFFAOYSA-N 0.000 description 1
- RLZLXWRTPKQCCY-UHFFFAOYSA-N Cc(ccc(C(N(C1)CC1c(cc1)ccc1C#N)=O)c1)c1-c1nc2cc(N3CCCC3)ncc2[nH]1 Chemical compound Cc(ccc(C(N(C1)CC1c(cc1)ccc1C#N)=O)c1)c1-c1nc2cc(N3CCCC3)ncc2[nH]1 RLZLXWRTPKQCCY-UHFFFAOYSA-N 0.000 description 1
- JGZAGNUDYHJTLK-UHFFFAOYSA-N Cc(ccc(C(N(C1)CC1c(cc1)ccc1C#N)=O)c1)c1-c1nc2cc(N3CCOCC3)ncc2[nH]1 Chemical compound Cc(ccc(C(N(C1)CC1c(cc1)ccc1C#N)=O)c1)c1-c1nc2cc(N3CCOCC3)ncc2[nH]1 JGZAGNUDYHJTLK-UHFFFAOYSA-N 0.000 description 1
- UZHLUTIBMWCOLA-UHFFFAOYSA-N Cc1c(-c2c(C)cc(C)c(C(N(C3)CC3(c3ccc(C)cc3)F)=O)c2)[nH]nc1C(N(C)C)=O Chemical compound Cc1c(-c2c(C)cc(C)c(C(N(C3)CC3(c3ccc(C)cc3)F)=O)c2)[nH]nc1C(N(C)C)=O UZHLUTIBMWCOLA-UHFFFAOYSA-N 0.000 description 1
- FJUULVZLLBBAFY-UHFFFAOYSA-N Cc1c(-c2c(C)cc(C)c(C(N(C3)CC3c(cc3)ccc3C#N)=O)c2)[nH]nc1C(N(C)C)=O Chemical compound Cc1c(-c2c(C)cc(C)c(C(N(C3)CC3c(cc3)ccc3C#N)=O)c2)[nH]nc1C(N(C)C)=O FJUULVZLLBBAFY-UHFFFAOYSA-N 0.000 description 1
- MGDZQRRJAMGCME-UHFFFAOYSA-N Cc1ncc(-c(cc(cc2)C(N(CC3)CCC3c(cc3)ccc3C#N)=O)c2N2CCC2)[nH]1 Chemical compound Cc1ncc(-c(cc(cc2)C(N(CC3)CCC3c(cc3)ccc3C#N)=O)c2N2CCC2)[nH]1 MGDZQRRJAMGCME-UHFFFAOYSA-N 0.000 description 1
- HSJBGIMFXZFGQR-UHFFFAOYSA-N N#Cc1ccc(C2CNC2)cc1 Chemical compound N#Cc1ccc(C2CNC2)cc1 HSJBGIMFXZFGQR-UHFFFAOYSA-N 0.000 description 1
- ALYVOHCGUMOKSC-UHFFFAOYSA-N NC(CCNCC1)=C1N Chemical compound NC(CCNCC1)=C1N ALYVOHCGUMOKSC-UHFFFAOYSA-N 0.000 description 1
- XDZISMLBQSWRRL-UHFFFAOYSA-N Nc1cc(N2CCC2)ncc1N Chemical compound Nc1cc(N2CCC2)ncc1N XDZISMLBQSWRRL-UHFFFAOYSA-N 0.000 description 1
Classifications
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/337—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
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- A—HUMAN NECESSITIES
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- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/4155—1,2-Diazoles non condensed and containing further heterocyclic rings
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
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- A61K31/4164—1,3-Diazoles
- A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
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- A61K31/4196—1,2,4-Triazoles
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- A61K31/42—Oxazoles
- A61K31/422—Oxazoles not condensed and containing further heterocyclic rings
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- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
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- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
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- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- 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
- C07D401/02—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 two hetero rings
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- 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
- C07D403/10—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 carbon chain containing aromatic rings
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- C07D407/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing three or more hetero rings
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Virology (AREA)
- Immunology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Pulmonology (AREA)
- Hematology (AREA)
- Transplantation (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Hydrogenated Pyridines (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361919235P | 2013-12-20 | 2013-12-20 | |
| US61/919,235 | 2013-12-20 | ||
| PCT/US2014/071617 WO2015095767A1 (en) | 2013-12-20 | 2014-12-19 | Heterocyclic modulators of lipid synthesis and combinations thereof |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2017505291A JP2017505291A (ja) | 2017-02-16 |
| JP2017505291A5 JP2017505291A5 (https=) | 2018-02-08 |
| JP6820097B2 true JP6820097B2 (ja) | 2021-01-27 |
Family
ID=52302407
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016541077A Active JP6820097B2 (ja) | 2013-12-20 | 2014-12-19 | 脂質合成の複素環式モジュレータ及びその組み合わせ |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US10226449B2 (https=) |
| EP (1) | EP3083583B1 (https=) |
| JP (1) | JP6820097B2 (https=) |
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| US20170119786A1 (en) | 2011-03-08 | 2017-05-04 | 3-V Biosciences, Inc. | Heterocyclic modulators of lipid synthesis |
| NZ703162A (en) * | 2012-07-03 | 2017-05-26 | 3-V Biosciences Inc | Heterocyclic modulators of lipid synthesis |
| JP6691909B2 (ja) | 2014-08-15 | 2020-05-13 | サギメット バイオサイエンシーズ インコーポレイテッド | 薬物耐性癌の治療で用いるための脂肪酸シンターゼ阻害剤 |
| WO2016149271A1 (en) * | 2015-03-19 | 2016-09-22 | 3-V Biosciences, Inc. | Heterocyclic modulators of lipid synthesis |
| WO2016168633A1 (en) | 2015-04-17 | 2016-10-20 | Abbvie Inc. | Indazolones as modulators of tnf signaling |
| KR102644934B1 (ko) | 2016-11-11 | 2024-03-08 | 새지메트 바이오사이언시스, 인코포레이티드 | 지질 합성의 헤테로사이클릭 조절인자 |
| ES2928773T3 (es) | 2017-01-17 | 2022-11-22 | Heparegenix Gmbh | Inhibidores de proteína cinasas para fomentar la regeneración hepática o reducir o prevenir la muerte de hepatocitos |
| CN107163043A (zh) * | 2017-06-16 | 2017-09-15 | 上海毕得医药科技有限公司 | 一种吡唑并[1,5‑a]吡啶‑3‑羧酸酯衍生物的合成方法 |
| WO2019101511A1 (en) | 2017-11-23 | 2019-05-31 | Basf Se | Substituted trifluoromethyloxadiazoles for combating phytopathogenic fungi |
| CN109956973B (zh) * | 2017-12-25 | 2020-11-03 | 上海启甄环境科技有限公司 | 一种放射性同位素碳-14标记毒氟磷的合成方法 |
| CN109503575B (zh) * | 2018-12-20 | 2021-01-29 | 温州大学 | 无催化剂N-N偶联反应合成[1,2,3]三氮唑[1,5-a]吡啶类化合物的方法 |
| CN111592495A (zh) * | 2020-07-06 | 2020-08-28 | 上海启讯医药科技有限公司 | 一种2-正丁基-4-氯-5甲酰基咪唑的制备方法 |
| GB202213166D0 (en) | 2022-09-08 | 2022-10-26 | Cambridge Entpr Ltd | Novel compounds, compositions and therapeutic uses thereof |
| CN116482278B (zh) * | 2023-05-06 | 2024-02-09 | 广州清瑞生物科技有限责任公司 | 一种用于检测阿昔洛韦的对照品的制备方法 |
| CN119080742A (zh) * | 2023-06-05 | 2024-12-06 | 甘莱制药有限公司 | 脂质合成的杂环调节剂的工业化制备 |
| WO2025080818A1 (en) * | 2023-10-10 | 2025-04-17 | Sagimet Biosciences Inc. | Combinations of fasn inhibitors and glp-1 agonists for liver diseases |
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| US4906474A (en) | 1983-03-22 | 1990-03-06 | Massachusetts Institute Of Technology | Bioerodible polyanhydrides for controlled drug delivery |
| US4789734A (en) | 1985-08-06 | 1988-12-06 | La Jolla Cancer Research Foundation | Vitronectin specific cell receptor derived from mammalian mesenchymal tissue |
| EP0545913B1 (en) | 1986-08-18 | 1999-02-24 | Emisphere Technologies, Inc. | Delivery systems for pharmacological agents |
| US5811128A (en) | 1986-10-24 | 1998-09-22 | Southern Research Institute | Method for oral or rectal delivery of microencapsulated vaccines and compositions therefor |
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| US4897268A (en) | 1987-08-03 | 1990-01-30 | Southern Research Institute | Drug delivery system and method of making the same |
| EP0678034B1 (en) | 1993-01-11 | 1999-05-26 | Dana Farber Cancer Institute | Inducing cytotoxic t lymphocyte responses |
| CA2517256C (en) | 2003-02-26 | 2013-04-30 | Sugen, Inc. | Aminoheteroaryl compounds as protein kinase inhibitors |
| WO2007063012A1 (en) | 2005-12-01 | 2007-06-07 | F. Hoffmann-La Roche Ag | Heteroaryl substituted piperidine derivatives as l-cpt1 inhibitors |
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| WO2008059214A1 (en) * | 2006-11-13 | 2008-05-22 | Astrazeneca Ab | Bisamlde derivatives and use thereof as fatty acid synthase inhibitors |
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| JP5557832B2 (ja) | 2008-03-18 | 2014-07-23 | メルク・シャープ・アンド・ドーム・コーポレーション | 置換4−ヒドロキシピリジン−5−カルボキサミド |
| JP2011527677A (ja) | 2008-07-08 | 2011-11-04 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Nhe−1阻害剤として有用なピロリジニル及びピペリジニル化合物 |
| JO3041B1 (ar) | 2008-07-25 | 2016-09-05 | Galapagos Nv | مركبات جديدة مفيدة لمعالجة الأمراض التنكسية والالتهابية |
| US8324250B2 (en) | 2009-03-19 | 2012-12-04 | Hoffmann-La Roche Inc. | Piperidine derivatives as NK3 receptor antagonists |
| US8748950B2 (en) | 2009-11-19 | 2014-06-10 | University of Pittsburgh—of the Commonwealth System of Higher Education | On-demand nanoelectronics platform |
| US8633183B2 (en) | 2010-01-26 | 2014-01-21 | Boehringer Ingelheim International Gmbh | 5-alkynyl-pyrimidines |
| US8871790B2 (en) * | 2011-03-08 | 2014-10-28 | 3-V Biosciences, Inc. | Heterocyclic modulators of lipid synthesis |
| WO2012122391A1 (en) * | 2011-03-08 | 2012-09-13 | 3-V Biosciences, Inc. | Heterocyclic modulators of lipid synthesis |
| US8604016B2 (en) * | 2011-11-21 | 2013-12-10 | Calithera Biosciences Inc. | Heterocyclic inhibitors of glutaminase |
| NZ703162A (en) * | 2012-07-03 | 2017-05-26 | 3-V Biosciences Inc | Heterocyclic modulators of lipid synthesis |
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| EP3083583B1 (en) | 2020-11-18 |
| CN106061963B (zh) | 2019-10-22 |
| US20160338998A1 (en) | 2016-11-24 |
| US10226449B2 (en) | 2019-03-12 |
| EP3083583A1 (en) | 2016-10-26 |
| ES2841137T3 (es) | 2021-07-07 |
| AU2014368945C1 (en) | 2019-05-16 |
| AU2014368945B2 (en) | 2019-01-24 |
| AU2014368945A1 (en) | 2016-06-16 |
| WO2015095767A1 (en) | 2015-06-25 |
| JP2017505291A (ja) | 2017-02-16 |
| CA2934251C (en) | 2024-01-02 |
| KR20160100329A (ko) | 2016-08-23 |
| CN106061963A (zh) | 2016-10-26 |
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