微管蛋白
长春碱
去肽
GTP'
抗真菌
肽
微管
生物
化学
药理学
立体化学
生物化学
微生物学
酶
化疗
细胞生物学
遗传学
作者
George R. Pettit,Jayaram K. Srirangam,József Barkóczy,M. D. Williams,Michael R. Boyd,Ernest Hamel,Robin K. Pettit,Fiona Hogan,Ruoli Bai,Jean Charles Chapuis,Shane C. McAllister,Jean M. Schmidt
出处
期刊:PubMed
日期:1998-06-01
卷期号:13 (4): 243-77
被引量:15
摘要
The remarkable anticancer drug dolastatin 10 (1a) from the Indian Ocean sea hare Dolabella auricularia is currently undergoing phase I clinical trials. Thirty-eight new structural modifications of this unusual peptide have been synthesized and evaluated against a variety of human and murine cancer cell lines, and for their ability to inhibit tubulin polymerization and vinblastine and GTP binding to tubulin. Dolastatin 10 and one structural modification was found to have antifungal activity, while one other structural modification of the parent compound exhibited antibacterial activity. Some of the new peptides approximated the antineoplastic potency of dolastatin 10, especially those based on replacement of the Doe unit with Met, Phe or an appropriately substituted phenylethylamide.
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