期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 130, 期 30, 页码 10019-10023出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja802803e
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Molecular design and chemical synthesis of several palmerolide A analogues allowed the first structure activity relationships (SARs) of this newly discovered marine antitumor agent. From several analogues synthesized and tested (ent-1, 5-14, 21-26, 50, 51), compounds 25 (with a phenyl substituent on the side chain) and 51 (lacking the C-7 hydroxyl group) were the most interesting, exhibiting approximately a 10-fold increase in potency and equipotency, respectively, to the natural product. These findings point the way to more focused structure activity relationship studies.
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