Synthesis and Antiproliferative Activity of Novel 1,2,3-Triazole-Sulfonamide Hybrids
作者:Na Li、Nan Liu、Shu Tang、Duo-Lu Li、Xiao-Jian Zhang
DOI:10.3184/174751918x15161933697853
日期:2018.1
Nine novel 1-(4′-sulfamoylphenyl)-1,2,3-triazole derivatives bearing an N-heterocycle moiety were designed using a molecular hybridisation approach and synthesised by alkyne/azide click chemistry. Most of the synthesised compounds exhibited good to moderate antiproliferative activity (IC50 values 3.7 to 77.1 μM) against stomach, oesophagus and prostate cancer cell lines, but a compound containing an
使用分子杂交方法设计了九种带有 N-杂环部分的新型 1-(4'-氨磺酰基苯基)-1,2,3-三唑衍生物,并通过炔烃/叠氮化物点击化学合成。大多数合成的化合物对胃、食道和前列腺癌细胞系表现出良好至中等的抗增殖活性(IC50 值为 3.7 至 77.1 μM),但含有 S-(2-吡啶基)硫甲基部分的化合物对抗增殖活性高 10 倍胃细胞系优于5-氟尿嘧啶。这些结果表明,N-杂环-1,2,3-三唑基磺酰胺可能是开发新型抗肿瘤药物的有前途的先导化合物。