发明名称 | Beta-lactamase inhibitors | ||
摘要 | Described herein are compounds and compositions that modulate the activity of beta-lactamases. In some embodiments, the compounds described herein inhibit beta-lactamase. In certain embodiments, the compounds described herein are useful in the treatment of bacterial infections. | ||
申请公布号 | US9637504(B2) | 申请公布日期 | 2017.05.02 |
申请号 | US201615162395 | 申请日期 | 2016.05.23 |
申请人 | VENATORX PHARMACEUTICALS, INC. | 发明人 | Burns Christopher J.;Daigle Denis;Liu Bin;Jackson Randy W.;Hamrick Jodie;McGarry Daniel;Pevear Daniel C.;Trout Robert E. Lee |
分类号 | C07F5/04;C07F5/02;A61K31/69;A61K45/06;A61K31/198 | 主分类号 | C07F5/04 |
代理机构 | Wilson, Sonsini, Goodrich & Rosati | 代理人 | Wilson, Sonsini, Goodrich & Rosati |
主权项 | 1. A compound of Formula (IIa) or a pharmaceutically acceptable salt, tautomer, or N-oxide thereof: wherein: M is hydrogen, —CN, —C(O)—R4, or optionally substituted alkynyl; each R1 and R2 are hydrogen; n is 0, 1, 2, 3, 4, 5, or 6; X1 is —OR4 or F; R3 is —R30OC(O)R31 or —R30OC(O)OR31; R30 is —CH2— or —CH(CH3)—; R31 is optionally substituted C1-C12 alkyl, aryl, C3-C8 cycloalkyl, or C3-C8 heterocycloalkyl; Ra, Rb, and Rc are independently hydrogen, fluoro, chloro, optionally substituted C1-C6 alkyl, —OR4, —NR4R5, or —SR4; Rd, R4 and R5 are independently hydrogen or C1-C6 alkyl. | ||
地址 | Malvern PA US |