Journal
JOURNAL OF HETEROCYCLIC CHEMISTRY
Volume 57, Issue 1, Pages 497-502Publisher
WILEY
DOI: 10.1002/jhet.3743
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Funding
- Natural Science Foundation of Shandong Province [ZR2013BM006]
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Substituted 4-chloroquinazoline reacted with sodium diselenide to give novel sodium quinazoline-4-diselenide compounds. The reaction provides an efficient and facile approach to the synthesis of sodium quinazoline-4-diselenide compounds. Structures of title compounds were confirmed by IR, H-1 NMR, C-13 NMR, and elemental analysis. MTT assay was adopted to show anticancer activities of the compounds. Compounds 5a and 5h showed good activities against cancer-cell lines MDA-MB-435, MDA-MB-231, A549, SiHa, and HeLa. In addition, 5a exhibited quite good anticancer effects on relative above cell lines with 10 mu M concentration compared with oxaliplatin and gefitinib of the commercial anticancer drugs.
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