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Synthesis and structure–activity relationships of sinenxan A derivatives as multidrug resistance reversal agents

✍ Scribed by Meng Huang; Xin Zhao; Meng Zhang; Jun Gu; Xiaoguang Chen; Dali Yin


Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
609 KB
Volume
20
Category
Article
ISSN
0960-894X

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✦ Synopsis


Two types of sinenxan A derivatives with different side chains at C-5 were synthesized and evaluated for their in vitro multidrug resistant reversal activities. Several derivatives exhibited better activities than the positive control verapamil. The structure-activity relationships of these derivatives suggested that a carbonyl group at C-13 and the length of side chain at C-5 are important for the activity.


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