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公开(公告)号:US11446280B2
公开(公告)日:2022-09-20
申请号:US16679313
申请日:2019-11-11
Applicant: Versitech Limited
Inventor: Yi Tsun Richard Kao , Peng Gao , Xuechen Li , Ming Liu
IPC: A61K31/40 , A61K31/496 , A61K31/47 , A61K31/454 , A61K31/4453 , A61K31/444 , A61K31/4406 , A61K31/4402 , A61K31/404 , A61K31/18 , A61K31/167 , A61K31/357 , A61P31/04 , C07D317/60 , C07D295/26
Abstract: Provided herein are compounds, derivatives thereof, and compositions including one or more of the compounds and derivatives, and methods for prevention and/or treatment of microbial infections and/or related diseases or conditions. The present compounds and/or derivatives thereof can be represented by Formula (I): The present methods include administering to a subject an effective amount of one or more compounds of Formula (I). In one embodiment, the microbial infections are bacterial infections. More specifically, the bacterial infections are staphylococcal infections.
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公开(公告)号:US11052078B2
公开(公告)日:2021-07-06
申请号:US16867540
申请日:2020-05-05
Applicant: Versitech Limited
Inventor: Yi Tsun Richard Kao , Peng Gao , Xuechen Li , Ming Liu
IPC: A61K31/4545 , A61K31/40 , A61K31/4453 , A61K31/404 , A61K31/47 , A61P31/04 , A61K31/18 , A61K31/4458 , A61K31/4462 , A61K31/496 , A61K31/472
Abstract: Provided herein are compounds, derivatives thereof, composition comprising one or more of said compounds and derivatives, and methods for prevention and/or treatment of microbial infections and/or related diseases or conditions. The present compounds and/or derivatives thereof can be represented by Formula (II): The present methods include administering to a subject an effective amount of one or more compounds of Formula (II). In one embodiment, said microbial infections are bacterial infections. More specifically, said bacterial infections are staphylococcal infections.
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公开(公告)号:US11040949B2
公开(公告)日:2021-06-22
申请号:US17006985
申请日:2020-08-31
Applicant: Versitech Limited
Inventor: Yi Tsun Richard Kao , Peng Gao , Xuechen Li , Ming Liu
IPC: C07D295/08 , A61K9/00 , C07D215/58 , C07D217/06 , A61P31/04
Abstract: Provided herein are compounds, derivatives thereof, composition comprising one or more of said compounds and derivatives, and methods for prevention and/or treatment of microbial infections and/or related diseases or conditions. The present compounds and/or derivatives thereof can be represented by Formula (II): The present methods include administering to a subject an effective amount of one or more compounds of Formula (II). In one embodiment, said microbial infections are bacterial infections. More specifically, said bacterial infections are staphylococcal infections.
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公开(公告)号:US10647746B2
公开(公告)日:2020-05-12
申请号:US15093950
申请日:2016-04-08
Applicant: Versitech Limited
Inventor: Xuechen Li
Abstract: Described are design and generation of a set of novel cyclic lipopeptides as potential antibacterial agents. New daptomycin analogues are generated by chemical synthesis, which makes introduction of an unnatural amino acid and any modification into daptomycin possible.
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公开(公告)号:US11667674B2
公开(公告)日:2023-06-06
申请号:US16310364
申请日:2017-03-24
Applicant: Versitech Limited
Inventor: Xuechen Li , Hoi Yee Chow
Abstract: Cyclic lipopeptides having one or more modifications relative to daptomycin, and methods of making them are provided. The cyclic lipopeptides can be used as antibacterial agents. The daptomycin analogues are generated by chemical synthesis, which makes introduction of an unnatural amino acid and any modification into daptomycin possible. Pharmaceutical compositions and method of use thereof for the disclosed daptomycin analogues are also provided.
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公开(公告)号:US20200010506A1
公开(公告)日:2020-01-09
申请号:US16310364
申请日:2017-03-24
Applicant: Versitech Limited
Inventor: Xuechen Li , Hoi Yee Chow
Abstract: Cyclic lipopeptides having one or more modifications relative to daptomycin, and methods of making them are provided. The cyclic lipopeptides can be used as antibacterial agents. The daptomycin analogues are generated by chemical synthesis, which makes introduction of an unnatural amino acid and any modification into daptomycin possible. Pharmaceutical compositions and method of use thereof for the disclosed daptomycin analogues are also provided.
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