Synthesis and biological evaluation of novel indenopyrazole derivatives
Abstract
A series of novel indenopyrazole derivatives 2a-j and 3a-j were synthesized from the reaction of 1-(4-(hydroxy(1-oxo-1,3-dihydro-2H-inden-2-ylidene)methyl)phenyl)-3-phenylurea derivatives 1a-j with hydrazine and phenylhydrazine, respectively. The obtained novel indenopyrazoles (2a-j and 3a-j) were evaluated for anticancer activity against HeLa and C6 cell lines. Antiproliferative activity was determined by the BrdU proliferation ELISA assay; 2a, 2b, 2d, 2h, and 3h were found to be the most active compounds. The compounds were also screened for antimicrobial activity, and all compounds showed moderate activity against used microorganisms.
Source
JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGYVolume
33Issue
5Collections
- Makale Koleksiyonu [5200]
- Makale Koleksiyonu [5745]
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