Structure-activity relationship study at the 3 '-N-position of paclitaxel: Synthesis and biological evaluation of 3 '-N-acyl-paclitaxel analogues
- Authors
 - Roh, EJ; Kim, D; Lee, CO; Choi, SU; Song, 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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