Staerk D, Lemmich E, Christensen J, Kharazmi A, Olsen C E, Jaroszewski J W
Department of Medicinal Chemistry, Royal Danish School of Pharmacy, Copenhagen, Denmark.
Planta Med. 2000 Aug;66(6):531-6. doi: 10.1055/s-2000-8661.
Five indole alkaloids, corynantheidine, corynantheine, dihydrocorynantheine, alpha-yohimbine and corynanthine were isolated from bark of Corynanthe pachyceras K. Schum. (Rubiaceae). The structures were established by spectroscopic methods, including previously unreported assignment of all 1H-NMR resonances by COSY and NOESY experiments. These and related alkaloids showed pronounced activity against Leishmania major promastigotes (IC50 at the micromolar level) but no significant in vitro antiplasmodial activity (against chloroquine-sensitive Plasmodium falciparum). Cytotoxicity assessed with drug sensitive KB-3-1 and multidrug-resistant KB-V1 cell lines was low; the alkaloids are apparently not substrates for the P-glycoprotein (P-170) efflux pump.
从厚角柯(茜草科)的树皮中分离出了5种吲哚生物碱,即柯楠定碱、柯楠碱、二氢柯楠碱、α-育亨宾和柯楠因。通过光谱方法确定了其结构,包括通过COSY和NOESY实验对所有1H-NMR共振进行了此前未报道的归属。这些生物碱及相关生物碱对硕大利什曼原虫前鞭毛体显示出显著活性(IC50处于微摩尔水平),但对氯喹敏感的恶性疟原虫没有显著的体外抗疟活性。用药物敏感的KB-3-1和多药耐药的KB-V1细胞系评估的细胞毒性较低;这些生物碱显然不是P-糖蛋白(P-170)外排泵的底物。