| Literature DB >> 21873049 |
Dalip Kumar1, N Maruthi Kumar, Kuei-Hua Chang, Ritika Gupta, Kavita Shah.
Abstract
A series of 3,5-bis(indolyl)-1,2,4-thiadiazoles were synthesized and evaluated for their cytotoxicity against selected human cancer cell lines. The reaction of indole-3-thiocarboxamide 3 with iodobenzene diacetate underwent oxidative dimerization to give 3,5-bis(indolyl)-1,2,4-thiadiazoles 4a-n. Among the synthesized bis(indoly)-1,2,4-thiadiazoles, the compound 4h with 4-chlorobenzyl and methoxy substituents showed the most potent activity.Entities:
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Year: 2011 PMID: 21873049 DOI: 10.1016/j.bmcl.2011.07.089
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823