Citation: Shi Ding, Wen-Ke Wang, Qiao Cao, Wen-Jing Chu, Le-Fu Lan, Wen-Hao Hu, Yu-She Yang. Design, synthesis and biological evaluation of LpxC inhibitors with novel hydrophilic terminus[J]. Chinese Chemical Letters, ;2015, 26(6): 763-767. doi: 10.1016/j.cclet.2015.03.029 shu

Design, synthesis and biological evaluation of LpxC inhibitors with novel hydrophilic terminus

  • Corresponding author: Yu-She Yang, 
  • Received Date: 18 December 2014
    Available Online: 17 March 2015

    Fund Project:

  • In order to develop novel LpxC inhibitors with good activities and metabolic stability, two series of compounds with hydrophilic terminus have been synthesized and their in vitro antibacterial activities against Escherichial coli and Pseudomonas aeruginosa were evaluated. Especially, compounds 22b and c exhibited comparable antibacterial activities to CHIR-090 and better metabolic stability than CHIR-090 and LPC-011 in liver microsomes (rat andmouse), which indicated the terminal methylsulfone may be a preferred structure in the design of LpxC inhibitors and worthy of further investigations.
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