Muriithi Mary W, Abraham W-R, Addae-Kyereme Jonathan, Scowen Ian, Croft Simon L, Gitu Peter M, Kendrick Howard, Njagi E N M, Wright Colin W
Department of Chemistry, University of Nairobi, Box 30197, Nairobi, Kenya.
J Nat Prod. 2002 Jul;65(7):956-9. doi: 10.1021/np0106182.
Seven alkaloids have been isolated from Teclea trichocarpa including four, normelicopicine (1), arborinine (2), skimmianine (6), and dictamnine (7), that are reported for the first time in addition to the previously reported alkaloids melicopicine (3), tecleanthine (4), and 6-methoxytecleanthine (5). The structure of 1 was confirmed by single-crystal X-ray crystallography. Two alkaloids, 1 and 2, displayed limited in vitro activities against Plasmodium falciparum strains HB3 and K1, but there appeared to be little cross-resistance with chloroquine. Alkaloid 1 was found to have some activity against P. berghei in mice (32% suppression of parasitaemia at a dose of 25 mg x kg(-1) x day(-1)), but unlike chloroquine it did not inhibit beta-haematin formation in a cell-free system; 1 was found to have low in vitro cytotoxicity to KB cells (IC50 > 328 microM).
从毛果茶(Teclea trichocarpa)中分离出了七种生物碱,其中包括四种,即降米仔兰碱(1)、乔木素(2)、茵芋碱(6)和白鲜碱(7),除了之前报道过的生物碱米仔兰碱(3)、茶梨碱(4)和6-甲氧基茶梨碱(5)外,这四种生物碱是首次被报道。化合物1的结构通过单晶X射线晶体学得以确证。两种生物碱,即1和2,对恶性疟原虫HB3和K1菌株显示出有限的体外活性,但与氯喹似乎几乎没有交叉耐药性。发现生物碱1对小鼠体内的伯氏疟原虫有一定活性(剂量为25 mg x kg(-1) x day(-1)时,疟原虫血症抑制率为32%),但与氯喹不同的是,它在无细胞体系中不抑制β-血红素的形成;发现1对KB细胞的体外细胞毒性较低(IC50 > 328 microM)。