| Literature DB >> 17154496 |
Jang-Yang Chang1, Hsing-Pang Hsieh, Chi-Yen Chang, Kuo-Shun Hsu, Yi-Fang Chiang, Chi-Ming Chen, Ching-Chuan Kuo, Jing-Ping Liou.
Abstract
A novel series of 7-aroyl-aminoindoline-1-benzenesulfonamides showed excellent activity as inhibitors of tubulin polymerization through binding with the colchicine binding site of microtubules. Compound 15 and 16 display IC50 values of 1.1 and 1.2 microM, respectively. Compound 15 inhibited the human cancer cell growth of KB, MKN45, H460, HT29, and TSGH, as well as one human-resistant cancer line of KB-vin 10, with an IC50 of 9.6, 8.8, 9.4, 8.6, 10.8, and 8.9 nM, respectively.Entities:
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Year: 2006 PMID: 17154496 DOI: 10.1021/jm061076u
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446