作者:Singanan Ponnuchamy、Selvaraj Kanchithalaivan、Raju Ranjith Kumar、Mohamed Ashraf Ali、Tan Soo Choon
DOI:10.1016/j.bmcl.2014.01.007
日期:2014.2
none were synthesized. These compounds were evaluated for their antimycobacterial activity against Mycobacterium tuberculosis H37Rv in High Throughput Screen. Most of the hybrid arylidene thiazolidine-2,4-diones displayed moderate to good activity with MIC of less than 50 μM. Compound 1m exhibited maximum potency being 5.87 fold more active at EC50 and 6.26 fold more active at EC90 than the standard
合成了一系列包括杂芳基噻唑烷-2,4-二酮和1-环丙基-2-(2-氟苯基)乙酮的杂合杂环。在高通量筛选中评估了这些化合物对结核分枝杆菌H 37 Rv的抗分枝杆菌活性。大多数杂化亚芳基噻唑烷-2,4-二酮显示中等至良好的活性,MIC小于50μM。与标准药物乙胺嘧啶相比,化合物1m的最大效价在EC 50上的活性高5.87倍,在EC 90上的活性高6.26倍。