Potent Inhibitors of LpxC for the Treatment of Gram-Negative Infections
摘要:
In this paper, we present the synthesis and SAR as well as selectivity, pharmacokinetic, and infection model data for representative analogues of a novel series of potent antibacterial LpxC inhibitors represented by hydroxamic acid 1a.
C-Linked Hydroxamic Acid Derivatives Useful As Antibacterial Agents
申请人:Brown Matthew Frank
公开号:US20120202777A1
公开(公告)日:2012-08-09
The present invention is directed to a new class of hydroxamic acid derivatives of Formula I,
wherein the variables G, T, D, L, A, X, R
1
and R
2
are as described hereinabove, and their use as LpxC inhibitors, and more specifically their use to treat bacterial infections.