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公开(公告)号:US11981696B2
公开(公告)日:2024-05-14
申请号:US16980616
申请日:2019-03-14
Applicant: Pfizer Inc.
Inventor: Tamim Fehme Braish , Matthew Frank Brown , Ye Che , Richard Andrew Ewin , Timothy Allan Johnson , Michael Joseph Melnick , Justin Ian Montgomery , Mark Stephen Plummer , Loren Michael Price , Usa Reilly , Daniel Uccello
Abstract: The present invention is directed to a new fluoro-pyridinone hydroxamic acid phosphates and boronates of Formulae I, II and III
wherein Q is selected from the group consisting of —P(O)(OH)2, —P(O)(OH)(O−M+), —P(O)(O−M+)2 and —P(O)(O−)2M2+; M+ at each occurrence is a pharmaceutically acceptable monovalent cation; and M2+ is a pharmaceutically acceptable divalent cation and their use as LpxC inhibitors and, more specifically, their use to treat bacterial infections.-
公开(公告)号:US20210017205A1
公开(公告)日:2021-01-21
申请号:US16980616
申请日:2019-03-14
Applicant: Pfizer Inc.
Inventor: Tamim Fehme Braish , Matthew Frank Brown , Ye Che , Richard Andrew Ewin , Timothy Allan Johnson , Michael Joseph Melnick , Justin Ian Montgomery , Mark Stephen Plummer , Loren Michael Price , Usa Reilly , Daniel Uccello
Abstract: The present invention is directed to a new fluoro-pyridinone hydroxamic acid phosphates and boronates of Formulae I, II and III wherein Q is selected from the group consisting of —P(O)(OH)2, —P(O)(OH)(O−M+), —P(O)(O−M+)2 and —P(O)(O−)2M2+; M+ at each occurrence is a pharmaceutically acceptable monovalent cation; and M2+ is a pharmaceutically acceptable divalent cation and their use as LpxC inhibitors and, more specifically, their use to treat bacterial infections.
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