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公开(公告)号:US20240287001A9
公开(公告)日:2024-08-29
申请号:US18029842
申请日:2021-10-01
申请人: Azafaros B.V.
发明人: Robert Hett , Fritz Blatter , Jennifer Robin , Kyle Landskroner
IPC分类号: C07D211/46
CPC分类号: C07D211/46 , C07B2200/13
摘要: The present invention relates to a crystalline form of compound (I) and a method of making the crystalline form of compound (I). The invention also provides pharmaceutical compositions comprising the crystalline form of compound (I). Furthermore, the invention relates to methods of using this crystalline form of compound (I) as a medicament and in the treatment of a disease involving abnormal levels of glucosylceramide and/or higher levels of glycosphingolipids.
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公开(公告)号:US11964942B2
公开(公告)日:2024-04-23
申请号:US17737580
申请日:2022-05-05
发明人: Zaifang Ren , Xuefeng Sun , Qing Xu
IPC分类号: C07D211/46 , C07C317/32 , C07D211/32 , C07D307/14 , C07D309/06 , C07D319/12
CPC分类号: C07D211/46 , C07C317/32 , C07D211/32 , C07D307/14 , C07D309/06 , C07D319/12
摘要: The application relates to a compound of Formula (I′) or (I):
or a pharmaceutically acceptable salt, hydrate, solvate, prodrug, stereoisomer, or tautomer thereof, which modulates the activity of SSAO, a pharmaceutical composition comprising a compound of Formula (I′) or (I), and a method of treating or preventing a disease in which SSAO plays a role.-
公开(公告)号:US11891369B2
公开(公告)日:2024-02-06
申请号:US16861166
申请日:2020-04-28
申请人: SRX Cardio, LLC
IPC分类号: A61K31/4709 , C07D295/073 , C07D401/04 , C07D403/04 , C07D211/18 , C07D211/26 , C07D211/46 , C07D211/54 , C07D211/58 , C07D295/195 , C07D401/12 , C07D401/14 , C07D405/14 , C07D407/02 , C07D417/04 , C07D417/14 , C07D471/08
CPC分类号: C07D295/073 , C07D211/18 , C07D211/26 , C07D211/46 , C07D211/54 , C07D211/58 , C07D295/195 , C07D401/04 , C07D401/12 , C07D401/14 , C07D403/04 , C07D405/14 , C07D407/02 , C07D417/04 , C07D417/14 , C07D471/08
摘要: The present disclosure relates to novel compounds, methods, and compositions capable of binding to PCSK9, thereby modulating PCSK9 proprotein convertase enzyme activity, for treatment of a disease or condition mediated, at least in part, by PCSK9. The compounds of the disclosure include compounds Formula (I).
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公开(公告)号:US11873288B2
公开(公告)日:2024-01-16
申请号:US17112713
申请日:2020-12-04
发明人: Bruce Hammock , Sean Kodani
IPC分类号: C07D401/06 , C07C275/28 , C07D271/10 , C07C275/34 , A61P35/00 , C07C275/36 , C07D211/16 , C07D211/46 , C07D401/12 , C07D401/14 , C07D413/14 , C07D417/04
CPC分类号: C07D401/06 , A61P35/00 , C07C275/28 , C07C275/34 , C07C275/36 , C07D211/16 , C07D211/46 , C07D271/10 , C07D401/12 , C07D401/14 , C07D413/14 , C07D417/04 , C07C2601/14
摘要: The present invention provides compounds that are dual inhibitors of soluble epoxide hydrolase and fatty acid amide hydrolase. The present invention also provides methods of using the compounds to inhibit soluble epoxide hydrolase and fatty acid amide hydrolase, and to treat cancer.
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公开(公告)号:US11767303B2
公开(公告)日:2023-09-26
申请号:US17384051
申请日:2021-07-23
申请人: Health Research, Inc. , Arizona Board of Regents on Behalf of the University of Arizona , Board of Regents, The University of Texas System
发明人: Hongmin Li , Zhong Li , Jia Zhou , Jimin Xu , Qing-Yu Zhang
IPC分类号: A61K31/5375 , C07D265/30 , C07C233/75 , C07D211/46 , A61P31/14 , C07D409/12 , C07D213/75 , C07D333/54
CPC分类号: C07D265/30 , A61P31/14 , C07C233/75 , C07D211/46 , C07D213/75 , C07D333/54 , C07D409/12
摘要: The present disclosure relates to a compound of formula (I) or a pharmaceutically acceptable salt thereof. The present disclosure further relates to methods of inhibiting viral replication including contacting one or more cells that have been infected with a virus with an effective amount of a compound of formula (I) or a pharmaceutically acceptable salt thereof, wherein the virus comprises a flavivirus. Also disclosed is a method of treating and/or preventing a flavivirus infection and/or a condition resulting from a flavivirus infection including administering an effective amount of a compound of formula (I) or a pharmaceutically acceptable salt thereof under conditions effective to treat and/or prevent a flavivirus infection and/or a condition resulting from a flavivirus infection.
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公开(公告)号:US11685718B2
公开(公告)日:2023-06-27
申请号:US17551806
申请日:2021-12-15
发明人: Kamlesh Sheth , Sergey Tesler , James Cartwright , Clive King , Wendy Cross
IPC分类号: C07D211/46
CPC分类号: C07D211/46 , C07B2200/13
摘要: Provided are methods of producing Active Pharmaceutical Ingredient (API) grade migalastat hydrochloride, and for purifying intermediate grade migalastat hydrochloride. Further provided are methods of producing [(2R,3S,4R,5S)-1-butyl-2-(hydroxymethyl)piperidine-3,4,5-triol hydrochloride (lucerastat hydrochloride) and other 1-deoxygalactonojirimycin compounds, as well as methods of purifying intermediate grade lucerastat hydrochloride and other 1-deoxygalactonojirimycin compounds.
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公开(公告)号:US20230174486A1
公开(公告)日:2023-06-08
申请号:US17923875
申请日:2021-05-06
发明人: Ramesh KAUL , Ernest J. MCEACHERN , Jianyu SUN , David J. VOCADLO , Yuanxi ZHOU , Yongbao ZHU
IPC分类号: C07D211/46 , C07D401/06 , C07D409/06 , C07D405/10 , C07D417/14 , C07D401/14 , C07D405/06 , C07D401/10 , C07D413/10 , C07D413/14
CPC分类号: C07D211/46 , C07D401/06 , C07D401/10 , C07D401/14 , C07D405/06 , C07D405/10 , C07D409/06 , C07D413/10 , C07D413/14 , C07D417/14
摘要: The invention provides compounds for inhibiting glucosylceramidases, prodrugs of the compounds, and pharmaceutical compositions including the compounds or prodrugs of the compounds.
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公开(公告)号:US20230090562A1
公开(公告)日:2023-03-23
申请号:US17813382
申请日:2022-07-19
发明人: ADAM GALAN , WENDY LUO , RITU LAL
IPC分类号: C07D491/107 , A61P31/14 , C07D207/12 , C07D211/42 , C07D211/46 , C07D239/30 , C07D241/08 , C07D265/30 , C07D267/10 , C07D491/048 , C07D498/18
摘要: Disclosed herein are p38α mitogen-activated protein kinase inhibitors, pharmaceutical compositions thereof, and therapeutic methods of using the p38α mitogen-activated protein kinase inhibitors.
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公开(公告)号:US20220411371A1
公开(公告)日:2022-12-29
申请号:US17762443
申请日:2020-09-23
IPC分类号: C07D211/46
摘要: The present disclosure encompasses solid state forms of Lucerastat, in embodiments crystalline Lucerastat: L-Pyroglutamic acid, crystalline Lucerastat: Salicylic acid, crystalline Lucerastat: Fumaric acid, crystalline Lucerastat: Benzoic acid and crystalline Lucerastat: o-Acetylsalicylic acid, solid state form thereof, processes for preparation thereof, and pharmaceutical compositions thereof.
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公开(公告)号:US20220127532A1
公开(公告)日:2022-04-28
申请号:US17431045
申请日:2020-02-14
申请人: MERCK PATENT GMBH
发明人: Helmut HAENSEL , Qiong TONG , Rocco FORTTE , Edward PLUMMER , Thomas EICHHORN
IPC分类号: C09K19/54 , C08F222/26 , C09K19/30 , C07D211/94 , C07D211/46 , C07D319/06 , C07C69/533
摘要: The present invention relates to polymerisable compounds, to processes and intermediates for the preparation thereof, to liquid-crystal (LC) media comprising them, and to the use of the polymerisable compounds and LC media for optical, electro-optical and electronic purposes, in particular in LC displays, especially in LC displays of the polymer sustained alignment (PS, PSA) and self-aligning (SA) type.
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