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Paclitaxel analogues from Taxus x media cv. Hicksii
B Gabetta1, N Fuzzati, P Orsini
1Indena S.p.A, via Don Minzoni 6, 20090 Settala (MI), Dipartimento di Scienza e Tecnologia del Farmaco, via Giuria 9, 10125 Torino, Italy. speclab@tin.it
Journal of Natural Products
|March 17, 1999
Abstract:
The roots of T. x media Rehd. cv. Hicksii gave three novel analogues of paclitaxel modified at the N-acyl residue (N-debenzoyl-N-alpha-methylbutyryl paclitaxel and N-debenzoyl-N-cinnamoyl paclitaxel, 1b and 1c, respectively) or at the ester group at C-2 (2-debenzoyl-2-tigloyl paclitaxel, 1d). Compounds 1b and 1d showed reduced cytotoxicity and tubulin binding compared to paclitaxel, while 1c retained substantial activity in these assays.