Bergstrom J D, Kurtz M M, Rew D J, Amend A M, Karkas J D, Bostedor R G, Bansal V S, Dufresne C, VanMiddlesworth F L, Hensens O D
Department of Biochemical Regulation, Merck Research Laboratories, Rahway, NJ 07065-0900.
Proc Natl Acad Sci U S A. 1993 Jan 1;90(1):80-4. doi: 10.1073/pnas.90.1.80.
Three closely related fungal metabolites, zaragozic acids A, B, and C, that are potent inhibitors of squalene synthase have been isolated and characterized. Zaragozic acids A, B, and C were produced from an unidentified sterile fungal culture, Sporormiella intermedia, and Leptodontium elatius, respectively. The structures of the zaragozic acids and their trimethyl esters were determined by a combination of physical and chemical techniques. The zaragozic acids are characterized by a novel 2,8-dioxobicyclo[3.2.1]octane-4,6,7- trihydroxyl-3,4,5-tricarboxylic acid core and differ from each other in the structures of the 6-acyl and 1-alkyl side chains. They were found to be potent competitive inhibitors of rat liver squalene synthase with apparent Ki values of 78 pM, 29 pM, and 45 pM, respectively. They inhibited cholesterol synthesis in Hep G2 cells, and zaragozic acid A was an inhibitor of acute hepatic cholesterol synthesis in the mouse (50% inhibitory dose of 200 micrograms/kg of body weight). Inhibition of squalene synthase in cells and in vivo was accompanied by an accumulation of label from [3H]mevalonate into farnesyl diphosphate, farnesol, and organic acids. These data indicate that the zaragozic acids are a previously unreported class of therapeutic agents with potential for the treatment of hypercholesterolemia.
三种密切相关的真菌代谢产物——扎拉戈酸A、B和C,它们是角鲨烯合酶的强效抑制剂,已被分离和鉴定。扎拉戈酸A、B和C分别由一种未鉴定的无菌真菌培养物、中间孢囊霉和纤细齿梗孢产生。通过物理和化学技术相结合的方法确定了扎拉戈酸及其三甲酯的结构。扎拉戈酸的特征是具有一个新颖的2,8 - 二氧代双环[3.2.1]辛烷 - 4,6,7 - 三羟基 - 3,4,5 - 三羧酸核心,它们在6 - 酰基和1 - 烷基侧链的结构上彼此不同。它们被发现是大鼠肝脏角鲨烯合酶的强效竞争性抑制剂,其表观Ki值分别为78 pM、29 pM和45 pM。它们抑制Hep G2细胞中的胆固醇合成,并且扎拉戈酸A是小鼠急性肝脏胆固醇合成的抑制剂(半数抑制剂量为200微克/千克体重)。细胞和体内角鲨烯合酶的抑制伴随着[3H]甲羟戊酸的标记物积累到法呢基二磷酸、法呢醇和有机酸中。这些数据表明扎拉戈酸是一类以前未报道过的具有治疗高胆固醇血症潜力的治疗剂。