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作为一类新型微管蛋白聚合抑制剂的2-吲哚基恶唑啉的合成及生物学评价。发现A-289099作为一种口服活性抗肿瘤剂。

Synthesis and biological evaluation of 2-indolyloxazolines as a new class of tubulin polymerization inhibitors. Discovery of A-289099 as an orally active antitumor agent.

作者信息

Li Qun, Woods Keith W, Claiborne Akiyo, Gwaltney Stephen L, Barr Kenneth J, Liu Gang, Gehrke Laura, Credo R Bruce, Hui Yu Hua, Lee Jang, Warner Robert B, Kovar Peter, Nukkala Michael A, Zielinski Nicolette A, Tahir Stephen K, Fitzgerald Michael, Kim Ki H, Marsh Kennan, Frost David, Ng Shi-Chung, Rosenberg Saul, Sham Hing L

机构信息

Cancer Research, Abbott Laboratories, 60064-6101, Abbott Park, IL 60064-6101, USA.

出版信息

Bioorg Med Chem Lett. 2002 Feb 11;12(3):465-9. doi: 10.1016/s0960-894x(01)00759-4.

Abstract

A series of indole containing oxazolines has been discovered as a result of structural modifications of the lead compound A-105972. The compounds exert their anticancer activity through inhibition of tubulin polymerization by binding at the colchicine site. A-289099 was identified as an orally active antimitotic agent active against various cancer cell lines including those that express the MDR phenotype. The anticancer activity, pharmacokinetics, and an efficient and enantioselective synthesis of A-289099 are described.

摘要

通过对先导化合物A-105972进行结构修饰,发现了一系列含吲哚的恶唑啉。这些化合物通过在秋水仙碱位点结合来抑制微管蛋白聚合,从而发挥其抗癌活性。A-289099被鉴定为一种口服活性抗有丝分裂剂,对包括那些表达多药耐药(MDR)表型的各种癌细胞系均有活性。本文描述了A-289099的抗癌活性、药代动力学以及一种高效且对映选择性的合成方法。

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