期刊
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 12, 期 3, 页码 371-374出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0960-894X(01)00757-0
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Eight analogues of (-)-16-chloro-1-dehydro-6S-bromovincadifformine 1 were synthesized and evaluated for cytotoxicity in L1210 cell culture. None of the new compounds was more active than 1 but the modulation at C6, C16 and on the aromatic ring at C10 informs about structure-activity relationships within this series. (C) 2002 Elsevier Science Ltd. All rights reserved.
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