Jantan Ibrahim, Pisar Mazura Md, Idris Muhammad Sum, Taher M, Ali Rasadah Mat
Department of Pharmacy, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.
Planta Med. 2002 Dec;68(12):1133-4. doi: 10.1055/s-2002-36343.
Rubraxanthone and isocowanol isolated from Garcinia parvifolia Miq. were investigated for their inhibitory effects on platelet-activating factor (PAF) binding to rabbit platelets using 3H-PAF as a ligand. Rubraxanthone showed a strong inhibition with IC 50 value of 18.2 microM. The IC 50 values of macluraxanthone, 6-deoxyjacareubin, 2-(3-methylbut-2-enyl)-1,3,5-trihydroxyxanthone, 2-(3-methylbut-2-enyl)-1,3,5,6-tetrahydroxyxanthone and 1,3,5-trihydroxy-6,6'-dimethylpyrano(2',3':6,7)-4-(1,1-dimethylprop-2-enyl)-xanthone were also determined for comparison. In the course of our study on structure-activity relationship of xanthones, the results revealed that a geranyl group substituted at C-8 was beneficial to the binding while a hydroxylated prenyl group at C-4 resulted in a significant loss in binding to the PAF receptor.
对从小叶藤黄(Garcinia parvifolia Miq.)中分离得到的红藤黄醌和异柯楠醇,以3H-PAF作为配体,研究了它们对血小板活化因子(PAF)与兔血小板结合的抑制作用。红藤黄醌表现出强烈的抑制作用,IC50值为18.2微摩尔。还测定了桑橙素、6-脱氧紫铆红素、2-(3-甲基丁-2-烯基)-1,3,5-三羟基氧杂蒽酮、2-(3-甲基丁-2-烯基)-1,3,5,6-四羟基氧杂蒽酮和1,3,5-三羟基-6,6'-二甲基吡喃并(2',3':6,7)-4-(1,1-二甲基丙-2-烯基)-氧杂蒽酮的IC50值以作比较。在我们对氧杂蒽酮结构-活性关系的研究过程中,结果表明,在C-8位取代的香叶基对结合有益,而在C-4位的羟基化异戊烯基会导致与PAF受体的结合显著丧失。