摘要

New N-acylhomoserine lactone (AHL) analogues in which the amide function is replaced by a reverse-amide one have been studied as AHL QS modulators. The series of compounds consists of alpha-(N-alkyl-carboxamide)- gamma-butyrolactones, alpha-(N-alkyl-sulfonamide)-gamma-butyrolactones, and 2-(N-alkyl-carboxamide)-cyclopentanones and cyclopentanols. Most active compounds exhibited antagonist activities against LuxR reaching the 30 mu M range.

  • 出版日期2011-11-15