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. 2006 Aug 3;8(16):3513-6.
doi: 10.1021/ol0611604.

Synthesis and biological evaluation of 10,11-methylenedioxy-14-azacamptothecin

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Synthesis and biological evaluation of 10,11-methylenedioxy-14-azacamptothecin

Mark A Elban et al. Org Lett. .

Abstract

[reaction: see text] 10,11-Methylenedioxy-14-azacamptothecin, a potent analogue of the antitumor agent camptothecin (CPT), has been prepared via a key condensation between AB and DE ring precursors. The biological testing of this compound validated a strategy for modulation of the off-rate of camptothecin analogues from the topoisomerase-DNA-CPT ternary complex via structural modification.

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