Abstract
A series of 3′- N-acyl-paclitaxel analogues 1a– v were synthesized and their cytotoxicities in vitro against several human tumor cell lines examined. It has been shown that distinct correlation between activity and N-acyl-substituent. The appropriate size of N-acyl group was indispensable for cytotoxicity, and moreover, the presence of β-substituted conjugated double and triple bond to N-carbonyl generally resulted in increase of cytotoxicities.
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