Institute of Pharmacy and Food Chemistry, University of Würzburg, Am Hubland, 97074 Würzburg, Germany.
Bioorg Med Chem Lett. 2010 Sep 15;20(18):5541-3. doi: 10.1016/j.bmcl.2010.07.062. Epub 2010 Aug 6.
Allicin and derivatives thereof inhibit the CAC1 cysteine proteases falcipain 2, rhodesain, cathepsin B and L in the low micromolar range. The structure-activity relationship revealed that only derivatives with primary carbon atom in vicinity to the thiosulfinate sulfur atom attacked by the active-site Cys residue are active against the target enzymes. Some compounds also show potent antiparasitic activity against Plasmodium falciparum and Trypanosoma brucei brucei.
大蒜素及其衍生物以低微摩尔浓度抑制疟原虫半胱氨酸蛋白酶 2、rhodesain、组织蛋白酶 B 和 L。结构-活性关系表明,只有在靠近活性部位半胱氨酸残基攻击的硫代亚磺酸硫原子的附近具有初级碳原子的衍生物才对靶酶具有活性。一些化合物对恶性疟原虫和布氏锥虫也表现出很强的抗寄生虫活性。