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公开(公告)号:US20240361688A1
公开(公告)日:2024-10-31
申请号:US18626972
申请日:2024-04-04
发明人: Masahiro Fukushima
IPC分类号: G03F7/004 , C07C25/18 , C07C211/63 , C07C381/12 , C07D207/16 , C07D211/46 , C07D211/54 , C07D211/62 , C07D221/14 , C07D327/08 , C07D333/76 , C07D405/12
CPC分类号: G03F7/0045 , C07C25/18 , C07C211/63 , C07C381/12 , C07D207/16 , C07D211/46 , C07D211/54 , C07D211/62 , C07D221/14 , C07D327/08 , C07D333/76 , C07D405/12
摘要: A chemically amplified resist composition is provided which is excellent in LWR and resolution and can prevent a resist pattern from collapsing in far ultraviolet lithography and EUV lithography, an onium salt for use therein, and a pattern forming process using the resist composition. The chemically amplified resist composition includes an onium salt having the following formula (1).
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公开(公告)号:US20240360129A1
公开(公告)日:2024-10-31
申请号:US18763258
申请日:2024-07-03
发明人: Stéphane DORICH , Jason BURCH , Miguel ST-ONGE , Amandine CHEFSON , Alexandre CÔTÉ , Ramsay BEVERIDGE , Stéphane CIBLAT
IPC分类号: C07D471/04 , A61K31/501 , A61K31/502 , A61K31/5025 , A61K31/5377 , C07D405/12 , C07D491/048 , C07D495/04 , C07D519/00
CPC分类号: C07D471/04 , A61K31/501 , A61K31/502 , A61K31/5025 , A61K31/5377 , C07D405/12 , C07D491/048 , C07D495/04 , C07D519/00
摘要: The present disclosure relates to inhibitors of NLRP3 useful in the treatment of diseases and disorders inhibited by said protein and having the Formula (I):
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公开(公告)号:US20240360128A1
公开(公告)日:2024-10-31
申请号:US18763243
申请日:2024-07-03
IPC分类号: C07D471/04 , A61K31/501 , A61K31/502 , A61K31/5025 , A61K31/5377 , C07D405/12 , C07D491/048 , C07D495/04 , C07D519/00
CPC分类号: C07D471/04 , A61K31/501 , A61K31/502 , A61K31/5025 , A61K31/5377 , C07D405/12 , C07D491/048 , C07D495/04 , C07D519/00
摘要: The present disclosure relates to inhibitors of NLRP3 useful in the treatment of diseases and disorders inhibited by said protein and having the Formula (I):
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公开(公告)号:US12128028B2
公开(公告)日:2024-10-29
申请号:US17258273
申请日:2019-07-05
发明人: Marc Rogers , Robert Kirby , Gakujun Shomi , Takuya Matsuo , Satoru Kobayashi , Junichiro Kanazawa , Nobutaka Yamaoka , Makoto Torizuka , Koichi Suzawa
IPC分类号: A61K31/4164 , A61K31/4178 , A61K31/439 , A61K31/4439 , A61K31/454 , A61K31/46 , A61K31/5377 , A61K31/55 , C07D233/28 , C07D235/02 , C07D401/06 , C07D401/12 , C07D403/06 , C07D403/12 , C07D405/12 , C07D409/12 , C07D471/08 , C07D491/107
CPC分类号: A61K31/4164 , A61K31/4178 , A61K31/439 , A61K31/4439 , A61K31/454 , A61K31/46 , A61K31/5377 , A61K31/55 , C07D233/28 , C07D235/02 , C07D401/06 , C07D401/12 , C07D403/06 , C07D403/12 , C07D405/12 , C07D409/12 , C07D471/08 , C07D491/107
摘要: The invention relates to heterocyclic sulfonamide derivatives and their use in the treatment and prophylaxis of autoimmune, inflammatory, cardiovascular, neuronal, auditory, renal and metabolic mediated diseases, and to compositions containing said derivatives and processes for their preparation.
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公开(公告)号:US20240343707A1
公开(公告)日:2024-10-17
申请号:US18631992
申请日:2024-04-10
发明人: Syed Kaleem Ahmed , Shilpa Dutta , Daniel N. Streblow , Corinne E. Augelli-Szafran , Omar Moukha-Chafiq , Ali Nakhi , Ashish Kumar Pathak
IPC分类号: C07D401/12 , A61K31/505 , A61K31/506 , A61K31/55 , A61K31/675 , A61P31/14 , C07D239/26 , C07D403/12 , C07D405/12 , C07D513/12 , C07F9/6512
CPC分类号: C07D401/12 , A61K31/505 , A61K31/506 , A61K31/55 , A61K31/675 , A61P31/14 , C07D239/26 , C07D403/12 , C07D405/12 , C07D513/12 , C07F9/6512
摘要: The present disclosure is concerned with substituted phenyl ethynyl pyrimidine compounds that are capable of inhibiting a viral infection and methods of treating alphavirus viral infections such as, for example, chikungunya, Eastern equine encephalitis (EEEV), Western equine encephalitis (WEEV), and Venezuelan equine encephalitis using these compounds. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
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公开(公告)号:US12116375B2
公开(公告)日:2024-10-15
申请号:US18490700
申请日:2023-10-19
发明人: Jonathan Ostrem , Ulf Peters , Kevan M. Shokat
IPC分类号: C07D409/04 , A61K38/17 , C07C235/20 , C07C317/08 , C07D207/14 , C07D211/58 , C07D211/62 , C07D231/40 , C07D295/185 , C07D295/26 , C07D401/04 , C07D401/06 , C07D401/12 , C07D405/12 , C07D413/12 , C07D417/12 , C07D471/10 , C07D487/04 , C07D487/10 , C07D495/04 , C12N9/14 , C12Q1/6886
CPC分类号: C07D495/04 , A61K38/1709 , C07C235/20 , C07C317/08 , C07D207/14 , C07D211/58 , C07D211/62 , C07D231/40 , C07D295/185 , C07D295/26 , C07D401/04 , C07D401/06 , C07D401/12 , C07D405/12 , C07D409/04 , C07D413/12 , C07D417/12 , C07D471/10 , C07D487/04 , C07D487/10 , C12N9/14 , C12Q1/6886 , C12Q2600/156 , C12Q2600/158 , C12Y306/05002 , G01N2500/04
摘要: K-Ras is the most frequently mutated oncogene in human cancer. Disclosed herein are compositions and methods for modulating K-Ras and treating cancer.
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公开(公告)号:US12116346B2
公开(公告)日:2024-10-15
申请号:US18136025
申请日:2023-04-18
发明人: Pravin L. Kotian , Yarlagadda S. Babu , Minwan Wu , Venkat R. Chintareddy , V. Satish Kumar , Weihe Zhang
IPC分类号: C07D231/14 , C07D401/04 , C07D401/12 , C07D401/14 , C07D403/04 , C07D403/12 , C07D405/12 , C07D413/04 , C07D413/12 , C07D417/12
CPC分类号: C07D231/14 , C07D401/04 , C07D401/12 , C07D401/14 , C07D403/04 , C07D403/12 , C07D405/12 , C07D413/04 , C07D413/12 , C07D417/12
摘要: Disclosed are compounds of formula I
as described herein, and pharmaceutically acceptable salts thereof. The compounds are inhibitors of plasma kallikrein. Also provided are pharmaceutical compositions comprising at least one compound of the invention, and methods involving use of the compounds and compositions of the invention in the treatment and prevention of diseases and conditions characterized by unwanted plasma kallikrein activity.-
公开(公告)号:US12115226B2
公开(公告)日:2024-10-15
申请号:US17271882
申请日:2019-08-28
发明人: Xinbo Zhou , Yanming Wang , Song Li , Wu Zhong , Shiyong Fan , Dian Xiao , Junhai Xiao , Zhibing Zheng , Xingzhou Li , Yunde Xie , Ruiyuan Cao , Xiaokui Wang
IPC分类号: A61K47/68 , A61K31/337 , A61K31/4745 , A61K31/537 , A61K31/5517 , A61K31/704 , A61K38/07 , A61K47/54 , A61P35/00 , C07C237/04 , C07D207/452 , C07D233/94 , C07D307/71 , C07D333/44 , C07D403/04 , C07D405/12 , C07D409/12
CPC分类号: A61K47/6811 , A61K31/337 , A61K31/4745 , A61K31/537 , A61K31/5517 , A61K31/704 , A61K38/07 , A61K47/545 , A61K47/6803 , A61K47/6809 , A61P35/00 , C07C237/04 , C07D207/452 , C07D233/94 , C07D307/71 , C07D333/44 , C07D403/04 , C07D405/12 , C07D409/12
摘要: The present application relates to a linker containing arylnitro, an antibody-drug conjugate the linker and use of the linker, as well as a pharmaceutical composition comprising the antibody-drug conjugate and use of the antibody-drug conjugate for treatment and/or prevention of a disease
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公开(公告)号:US20240336571A1
公开(公告)日:2024-10-10
申请号:US18749828
申请日:2024-06-21
发明人: Mark CHAPMAN , Nicholas Gareth Morse DAVIES , Aaron GERLACH , Christopher John GRAHAM , Sylvain LEBRETON , Ronghua LI , Nina MA , Daniel MADDOX , Ingrid MECHIN , David MOWREY , Karthigeyan NAGARAJAN , Anil NAIR , Roger David NORCROSS , Roger Lluis REDONDO PENA , Alena SAFAROVA , Martin SMRCINA
IPC分类号: C07D221/00 , A61K31/4433 , A61K31/4439 , C07D239/26 , C07D401/04 , C07D405/12 , C07D413/04 , C07D417/04
CPC分类号: C07D221/00 , A61K31/4433 , A61K31/4439 , C07D239/26 , C07D401/04 , C07D405/12 , C07D413/04 , C07D417/04
摘要: The invention provides new heterocyclic compounds having the general formula (I′), or a solvate or a pharmaceutically acceptable salt thereof:
wherein R1, R2, R3, R4, R5, R6, R7 and R8 are as defined herein, compositions including the compounds, processes of manufacturing the compounds and methods of using the compounds.-
公开(公告)号:US20240336570A1
公开(公告)日:2024-10-10
申请号:US18525253
申请日:2023-11-30
发明人: Marion Lanier , Marcus Boehm , Liming Huang , Esther Martinborough , Marcos Sainz , Brandon Selfridge , Adam Yeager
IPC分类号: C07D215/46 , C07D401/12 , C07D401/14 , C07D405/12 , C07D405/14 , C07D417/12 , C07D471/04 , C07D495/04 , C07D513/04
CPC分类号: C07D215/46 , C07D401/12 , C07D401/14 , C07D405/12 , C07D405/14 , C07D417/12 , C07D471/04 , C07D495/04 , C07D513/04
摘要: Methods are provided for modulating MRGPR X2 generally, or for treating a MRGPR X2 or a MRGPR X2 ortholog dependent condition, more specifically, by contacting the MRGPR X2 or the MRGPR X2 ortholog by administering to a subject in need thereof, respectively, an effective amount of a compound having structure (I):
or a pharmaceutically acceptable salt, isomer, hydrate, solvate or isotope thereof, wherein W, Z, R1, R2, R3, R4, R5, R6 and Rx are as defined herein. Pharmaceutical compositions containing such compounds, as well as the compounds themselves, are also provided.
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