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pubmed-article:16279766pubmed:abstractTextAnalogues of the natural product noscapine were synthesized and their potential as antitumor agents evaluated. The discovery of a novel regioselective O-demethylation facilitated the synthesis of the potent aniline 6, which arrests mammalian cells in the G2/M phase of the cell cycle at 0.1 microM and also affects tubulin polymerization. Aniline 6 is orally bioavailable and is 250-fold more potent than noscapine in reducing cell proliferation in rapidly dividing cells.lld:pubmed
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pubmed-article:16279766pubmed:articleTitleIdentification of novel and improved antimitotic agents derived from noscapine.lld:pubmed
pubmed-article:16279766pubmed:affiliationAthersys, Inc., 3201 Carnegie Avenue, Cleveland, Ohio 44115-2634, USA. janderson@athersys.comlld:pubmed
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