One-pot multicomponent synthesis of indole incorporated thiazolylcoumarins and their antibacterial, anticancer and DNA cleavage studies
作者:Rajitha Gali、Janardhan Banothu、Ramesh Gondru、Rajitha Bavantula、Yashodhara Velivela、Peter A. Crooks
DOI:10.1016/j.bmcl.2014.10.100
日期:2015.1
A series of indole incorporated thiazolylcoumarins (7a–q) have been synthesized and evaluated for their antibacterial, anticancer and DNA cleavage studies. Analysis of antibacterial studies indicated that all the synthesized compounds possess promising activity towards the screened bacterial strains. In vitro anticancerous action was studied for compound 7a (NSC: 768621/1) against the full panel of
已合成了一系列吲哚并入的噻唑基香豆素(7a - q),并对其抗菌,抗癌和DNA裂解研究进行了评估。抗菌研究的分析表明,所有合成的化合物均对筛选出的细菌菌株具有有希望的活性。研究了化合物7a(NSC:768621/1)对60种人类肿瘤细胞系的体外抗癌作用。五种剂量水平的活性结果表明,化合物7a对其中的所有细胞系均具有活性,并且已显示出对白血病的有效活性:CCRF-CEM(GI 50:0.33μM),非小细胞肺癌:NCI-H522 (GI 50:1.03μM),结肠癌:HCT-116(GI 50:1.60μM),CNS癌症:SF-539(GI 50:1.58μM),黑色素瘤MALME-3M(GI 50:1.59μM ),卵巢癌:OVCAR- 3(GI 50:1.16μM),肾癌:UO-31(GI 50:0.76μM),前列腺癌:PC-3(GI 50:0.82μM)和乳腺癌:BT-549(GI 50:1