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Updated: Jul 18, 2026

Optimizing Tubulin Yield from Porcine Brain Tissue
Published on: October 11, 2024
7-Aroyl-aminoindoline-1-sulfonamides as a novel class of potent antitubulin agents
Jang-Yang Chang1, Hsing-Pang Hsieh, Chi-Yen Chang
1Institute of Cancer Research, National Health Research Institutes, Taipei, Taiwan, Republic of China.
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.
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