| Literature DB >> 22954735 |
Weixia Li1, Nianguang Li, Yuping Tang, Baoquan Li, Li Liu, Xu Zhang, Haian Fu, Jin-Ao Duan.
Abstract
The anticancer activities of alkyl esters and NO-donors of ferulic acid (FA) and caffeic acid (CA) were assessed by a high-throughout screening (HTS) method, and the structure-activity relationships were described. CA alkyl esters had better anticancer activities than FA alkyl esters with the same alkyl substituent. Mono-nitrates and phenylfuroxan nitrates were more potent than the dual nitrates. Phenylsulfonylfuroxan nitrates of FA, especially compounds 8b-8d, exhibited more potent activities in anticancer.Entities:
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Year: 2012 PMID: 22954735 DOI: 10.1016/j.bmcl.2012.08.038
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823