| Literature DB >> 25938266 |
Hidemitsu Minegishi1,2, Yushi Futamura3, Shinji Fukashiro2, Makoto Muroi3, Makoto Kawatani3, Hiroyuki Osada3, Hiroyuki Nakamura1.
Abstract
A series of indenopyrazoles was synthesized from the corresponding indanones and phenyl isothiocyanates in two steps. Among the compounds synthesized, methyl 3-((6-methoxy-1,4-dihydroindeno[1,2-c]pyrazol-3-yl)amino)benzoate 6m (GN39482) was found to possess a promising antiproliferative activity toward human cancer cells without affecting any antimicrobial and antimalarial activities at 100 nM. Both a methoxy group at R(1) position and a methoxycarbonyl group at R(2) position of the anilinoquinazoline framework are essential for the high cell growth inhibition. Both MorphoBase and ChemProteoBase profiling analyses suggested that compound 6m was classified as a tubulin inhibitor. Indeed, compound 6m inhibited the acetylated tubulin accumulation and the microtubule formation and induced G2/M cell cycle arrest in HeLa cells, revealing that a promising antiproliferative activity of compound 6m toward human cancer cells is probably caused by the tubulin polymerization inhibition.Entities:
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Year: 2015 PMID: 25938266 DOI: 10.1021/acs.jmedchem.5b00035
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446