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公开(公告)号:US11426385B2
公开(公告)日:2022-08-30
申请号:US16641430
申请日:2018-08-14
申请人: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA , United States as represented by the Department of Veterans Affairs
发明人: Bruce D. Hammock , Sung Hee Hwang , Ralph W. de Vere White , Chong-xian Pan , Hongyong Zhang , Paul Henderson , Ai-Hong Ma , Maike Zimmermann , Fuli Wang
IPC分类号: A61K31/415 , A61P35/00 , A61K33/243 , A61K31/7068 , A61K45/06
摘要: Provided are methods and compositions for prolonging survival and/or reducing or inhibiting tumor growth in a cancer subject receiving a regimen of one or more chemotherapeutic agents, an inhibitor of soluble epoxide hydrolase (sEHi) and a non-steroidal anti-inflammatory drug (NSAID) that inhibits one or more enzymes selected from the group consisting of cyclo-oxygenase (“COX”)-1, COX-2, and 5-lipoxygenase (“5-LOX”). The methods and compositions decrease toxicity and/or adverse side effects in subjects receiving a regimen of one or more chemotherapeutic agents.
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公开(公告)号:US10449182B2
公开(公告)日:2019-10-22
申请号:US14408280
申请日:2013-06-20
IPC分类号: A61K31/44 , A61K31/4439 , A61K31/17 , A61K31/192 , A61K31/277 , A61P35/02 , A61P35/00 , A61K31/4412 , A61K45/06 , A61K31/196 , A61K31/675 , A61K31/704 , A61K33/24
摘要: The present invention provides sorafenib analogs for use in a method of treating a disease mediated by p21, said method comprising administering to a subject in need thereof a therapeutically effective amount of a compound of formula I. The present invention also provides methods of inhibiting p21 in a cell comprising contacting the cell with an effective amount of a compound of formula I.
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公开(公告)号:US20150132408A1
公开(公告)日:2015-05-14
申请号:US14408280
申请日:2013-06-20
IPC分类号: A61K31/4412 , A61K45/06 , A61K31/17 , A61K31/4439 , A61K31/196 , A61K31/277
CPC分类号: A61K31/4412 , A61K31/17 , A61K31/196 , A61K31/277 , A61K31/44 , A61K31/4439 , A61K31/675 , A61K31/704 , A61K33/24 , A61K45/06 , A61K2300/00
摘要: The present invention provides sorafenib analogs for use in a method of treating a disease mediated by p21, said method comprising administering to a subject in need thereof a therapeutically effective amount of a compound of formula I. The present invention also provides methods of inhibiting p21 in a cell comprising contacting the cell with an effective amount of a compound of formula I.
摘要翻译: 本发明提供了用于治疗由p21介导的疾病的方法的索拉非尼类似物,所述方法包括向有需要的受试者施用治疗有效量的式I化合物。本发明还提供了抑制p21的化合物的方法 包括使细胞与有效量的式I化合物接触的细胞。
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公开(公告)号:US10689595B2
公开(公告)日:2020-06-23
申请号:US16275293
申请日:2017-08-16
发明人: Guodong Zhang , Bruce Hammock , Sung Hee Hwang , Weicang Wang
IPC分类号: C11C3/12 , C11C3/14 , C07C67/343 , C07C67/303 , C07C51/09 , A61P35/00
摘要: The present invention provides a synthetic chemical method for preparing ω-hydroxylated polyunsaturated fatty acids (PUFAs) including 20-hydroxyeicosatetraenoic acid (20-HETE), 20-hydroxyeicosapentaenoic acid (20-HEPE), and 22-hydroxydocosahexaenoic acid (22-HDoHE) and a method of use thereof for treating cancer and macular degeneration.
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公开(公告)号:US20240342196A1
公开(公告)日:2024-10-17
申请号:US18634143
申请日:2024-04-12
IPC分类号: A61K31/64 , A61K31/202 , A61K31/4468 , A61P3/10
CPC分类号: A61K31/64 , A61K31/202 , A61K31/4468 , A61P3/10
摘要: Disclosed herein are lipid signaling pathways that can be targeted to prevent or delay the onset of type 1 diabetes (T1D). In particular, disclosed herein a pathway that can be modulated by a chemical inhibitor. Utilizing this inhibitor, evidence was generated suggesting that it is beneficial in reducing the incidence of T1D.
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公开(公告)号:US11001783B2
公开(公告)日:2021-05-11
申请号:US16867237
申请日:2020-05-05
发明人: Guodong Zhang , Bruce Hammock , Sung Hee Hwang , Weicang Wang
IPC分类号: A61P35/00 , C11C3/12 , C11C3/14 , C07C67/343 , C07C67/303 , C07C51/09
摘要: The present invention provides a synthetic chemical method for preparing ω-hydroxylated polyunsaturated fatty acids (PUFAs) including 20-hydroxyeicosatetraenoic acid (20-HETE), 20-hydroxyeicosapentaenoic acid (20-HEPE), and 22-hydroxydocosahexaenoic acid (22-HDoHE) and a method of use thereof for treating cancer and macular degeneration.
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