Semisynthesis and biological evaluation of a novel D-seco docetaxel analogue.

Org Lett

Institut de Chimie des Substances Naturelles-CNRS, Gif sur Yvette, France.

Published: May 2006

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Article Abstract

[reaction: see text] A 4-methyl-5-oxo docetaxel analogue has been prepared starting from 10-deacetylbaccatin III. This new D-seco docetaxel analogue is slightly less potent than docetaxel at microtubule stabilization in vitro and has about 1/1000th the cytotoxicity of docetaxel. The lack of improved activity for this compound compared to other D-modified taxoids confirms that a C-5 oxygen atom is not required for biological activity.

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http://dx.doi.org/10.1021/ol060531dDOI Listing

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text] 4-methyl-5-oxo
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