Pettit G R, Singh S B, Schmidt J M, Niven M L, Hamel E, Lin C M
Cancer Research Institute, Arizona State University, Tempe 85287.
J Nat Prod. 1988 May-Jun;51(3):517-27. doi: 10.1021/np50057a011.
Further investigation of a CH2Cl2 fraction prepared from the South African tree Combretum caffrum for substances inhibitory to the murine P-388 lymphocytic leukemia (PS system) cell line has led to the isolation of two new bibenzyls, designated combretastatins B-3 and B-4, accompanied by the previously known bibenzyls 7, 8, and 9. The structure of each substance was ascertained by results of mass and nmr spectral analyses and confirmed by crystal structure determination (for 7) or synthesis. Combretastatins B-3 and B-4 gave PS ED50 values of 0.4 and 1.7 micrograms/ml, respectively, and bibenzyls 7, 8, and 9 were comparably cell growth inhibitory against the PS cell line with ED50 results of 1.7, 2.5, and 0.25 ug/ml, respectively. All the bibenzyls caused leukemia cells to accumulate in mitosis at cytotoxic drug concentrations; however, a wide range of in vitro activity against the protein tubulin (the major component of the mitotic spindle) was observed.
对从南非树木南非风车子中制备的二氯甲烷馏分进行进一步研究,以寻找对小鼠P - 388淋巴细胞白血病(PS系统)细胞系具有抑制作用的物质,从而分离出两种新的联苄,命名为风车子素B - 3和风车子素B - 4,同时还分离出了之前已知的联苄7、8和9。每种物质的结构通过质谱和核磁共振光谱分析结果确定,并通过晶体结构测定(针对7)或合成得到证实。风车子素B - 3和风车子素B - 4对PS细胞系的ED50值分别为0.4和1.7微克/毫升,联苄7、8和9对PS细胞系的细胞生长抑制作用相当,ED50结果分别为1.7、2.5和0.25微克/毫升。在细胞毒性药物浓度下,所有联苄都会使白血病细胞在有丝分裂期积累;然而,观察到它们对蛋白质微管蛋白(有丝分裂纺锤体的主要成分)具有广泛的体外活性。