Kutterer Kristina M K, Davis Jamie M, Singh Guy, Yang Youjun, Hu William, Severin Anatoly, Rasmussen Beth A, Krishnamurthy Girija, Failli Amedeo, Katz Alan H
Wyeth Research, Chemical and Screening Sciences, 401 N. Middletown Rd, Pearl River, NY 10965, USA.
Bioorg Med Chem Lett. 2005 May 16;15(10):2527-31. doi: 10.1016/j.bmcl.2005.03.058.
Over 195 4-alkyl and 4,4-dialkyl 1,2-bis(4-chlorophenyl)pyrazolidine-3,5-dione derivatives were synthesized, utilizing microwave accelerated synthesis, for evaluation as new inhibitors of bacterial cell wall biosynthesis. Many of them demonstrated good activity against MurB in vitro and low MIC values against gram-positive bacteria, particularly penicillin-resistant Streptococcus pneumoniae (PRSP). Derivative 7l demonstrated antibacterial activity against both gram-positive and gram-negative bacteria. Derivatives 7f and 10a also demonstrated potent nanomolar Kd values in their binding to MurB.
利用微波加速合成法合成了195种以上的4-烷基和4,4-二烷基1,2-双(4-氯苯基)吡唑烷-3,5-二酮衍生物,以评估其作为细菌细胞壁生物合成新抑制剂的性能。其中许多化合物在体外对MurB表现出良好活性,对革兰氏阳性菌,尤其是耐青霉素肺炎链球菌(PRSP)的最低抑菌浓度值较低。衍生物7l对革兰氏阳性菌和革兰氏阴性菌均表现出抗菌活性。衍生物7f和10a在与MurB结合时也表现出纳摩尔级的有效解离常数(Kd)值。