Structure-activity relationship study at the 3 '-N-position of paclitaxel: Synthesis and biological evaluation of 3 '-N-acyl-paclitaxel analogues

Authors
Roh, EJKim, DLee, COChoi, SUSong, CE
Issue Date
2002-10
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
BIOORGANIC & MEDICINAL CHEMISTRY, v.10, no.10, pp.3145 - 3151
Abstract
A series of 3'-N-acyl-paclitaxel analogues la-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 beta-substituted conjugated double and triple bond to N-carbonyl generally resulted in increase of cytotoxicities. (C) 2002 Elsevier Science Ltd. All rights reserved.
Keywords
ANTITUMOR AGENTS; TAXOL; ANTITUMOR AGENTS; TAXOL; SAR
ISSN
0968-0896
URI
https://pubs.kist.re.kr/handle/201004/139185
DOI
10.1016/S0968-0896(02)00218-3
Appears in Collections:
KIST Article > 2002
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