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Merck
CN
  • Synthesis and in vitro antiproliferative evaluation of novel hybrids from 1,3,4-thiadiazole and benzisoselenazolone.

Synthesis and in vitro antiproliferative evaluation of novel hybrids from 1,3,4-thiadiazole and benzisoselenazolone.

Chemical & pharmaceutical bulletin (2015-06-02)
Fen Jing, Xiaoyun Fu, Sha Li, Baolin Li, Jijun Zhao, Xuefeng Wang, Yuming Liu, Baoquan Chen
摘要

Novel hybrids from 1,3,4-thiadiazole and benzisoselenazolone were designed, synthesized and evaluated for their in vitro antiproliferative activities by CCK-8 assay against three types of human cancer cell lines, SMMC-7721, MCF-7 and A549 cells. The preliminary bioassay results demonstrated that all tested compounds 4a-p showed potent antiproliferative activities, and some compounds exhibited better effects than positive control ethaselen and 5-fluorouracil (5-FU) against various cancer cell lines. Furthermore, compound 4g showed significant antiproliferative activities against SMMC-7721 cells with an IC50 value of 2.08 µM. Compounds 4b and 4m displayed highly effective biological activities against MCF-7 cells with an IC50 values of 2.03 and 2.06 µM, respectively. Compound 4i exhibited the best inhibitory effect against A549 cells with an IC50 value of 1.03 µM.

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Sigma-Aldrich
溴化钾, BioUltra, ≥99.5% (AT)
Sigma-Aldrich
溴化钾, anhydrous, powder, 99.999% trace metals basis
Sigma-Aldrich
溴化钾, anhydrous, powder, 99.95% trace metals basis
Sigma-Aldrich
溴化钾, BioXtra, ≥99.0%