Götz Marion G, Caffrey Conor R, Hansell Elizabeth, McKerrow James H, Powers James C
School of Chemistry and Biochemistry and the Petit Institute of Bioscience and Bioengineering, Georgia Institute of Technology, Atlanta, GA 30332-0400, USA.
Bioorg Med Chem. 2004 Oct 1;12(19):5203-11. doi: 10.1016/j.bmc.2004.07.016.
A new series of peptidyl allyl sulfone inhibitors was discovered while trying to synthesize epoxy sulfone inhibitors from vinyl sulfones using basic oxidizing conditions. The various dipeptidyl allyl sulfones were evaluated with calpain I, papain, cathepsins B and L, cruzain and rhodesain and found to be potent inhibitors. In comparison to the previously developed class of vinyl sulfone inhibitors, the novel dipeptidyl allyl sulfones were more potent inhibitors than the corresponding dipeptidyl vinyl sulfones. It was observed that the stereochemistry of the vinyl sulfone precursor played a role in the potency of the dipeptidyl allyl sulfone inhibitor.
在尝试使用碱性氧化条件从乙烯基砜合成环氧砜抑制剂的过程中,发现了一系列新的肽基烯丙基砜抑制剂。对各种二肽基烯丙基砜进行了针对钙蛋白酶I、木瓜蛋白酶、组织蛋白酶B和L、克鲁兹蛋白酶和罗得西亚蛋白酶的评估,发现它们是有效的抑制剂。与先前开发的乙烯基砜抑制剂类别相比,新型二肽基烯丙基砜是比相应的二肽基乙烯基砜更有效的抑制剂。据观察,乙烯基砜前体的立体化学在二肽基烯丙基砜抑制剂的效力中起作用。