Stachulski Andrew V, Berry Neil G, Lilian Low A C, Moores Shelley L, Row Eleanor, Warhurst David C, Adagu Ipemida S, Rossignol Jean-François
Romark Centre for Drug Discovery, Robert Robinson Laboratories, Department of Chemistry, University of Liverpool, Liverpool L69 7ZD, UK.
J Med Chem. 2006 Feb 23;49(4):1450-4. doi: 10.1021/jm050973f.
We report the preparation and antiparasitic activity in vitro and in vivo of a series of isoflavone derivatives related to genistein. These analogues retain the 5,7-dihydroxyisoflavone core of genistein: direct genistein analogues (2-H isoflavones), 2-carboethoxy isoflavones, and the precursor deoxybenzoins were all evaluated. Excellent in vitro activity against Cryptosporidium parvum was observed for both classes of isoflavones in cell cultures, and the lead compound 19, RM6427, shows high in vivo efficacy against an experimental infection.
我们报告了一系列与染料木黄酮相关的异黄酮衍生物的制备及其体外和体内抗寄生虫活性。这些类似物保留了染料木黄酮的5,7-二羟基异黄酮核心:直接的染料木黄酮类似物(2-H异黄酮)、2-乙氧羰基异黄酮以及前体脱氧安息香均经过了评估。在细胞培养中,两类异黄酮对微小隐孢子虫均表现出优异的体外活性,先导化合物19(RM6427)在实验性感染中显示出高体内疗效。