Design, Synthesis and Anticancer Screening of Novel Benzothiazole-Piperazine-1,2,3-Triazole Hybrids
作者:Mohamed Aouad、Moataz Soliman、Muath Alharbi、Sanaa Bardaweel、Pramod Sahu、Adeeb Ali、Mouslim Messali、Nadjet Rezki、Yaseen Al-Soud
DOI:10.3390/molecules23112788
日期:——
3-triazole based benzothiazole-piperazine conjugates were designed and synthesized using the click synthesis approach in the presence and absence of the Cu(I) catalyst. Some of these 1,2,3-triazole hybrids possess in their structures different heterocyclic scaffold including 1,2,4-triazole, benzothiazole, isatin and/or benzimidazole. The newly designed 1,2,3-triazole hybrids were assessed for their antiproliferative
在存在和不存在 Cu(I ) 催化剂。这些 1,2,3-三唑杂化物中的一些在其结构上具有不同的杂环支架,包括 1,2,4-三唑、苯并噻唑、靛红和/或苯并咪唑。评估了新设计的 1,2,3-三唑杂种对四种选定的人类癌细胞系(MCF7、T47D、HCT116 和 Caco2)的抗增殖抑制效力。大多数合成的化合物表现出对所有检查的癌细胞系的中等至强效活性。此外,我们已经建立了关于 ADME(吸附、分布、