Li Q, Shao H W, Jiang H L, Xie Y Y
Department of Synthetic Chemistry, Shanghai Institute of Materia Medica, Academia Sinica, P.R. of China.
Pharmazie. 1995 Jul;50(7):447-9.
The title compounds having the structure of 2,3-diacetoxy-4-carbomethoxy-(3',5'-dioxo-N4'-substituted piperazinyl methyl) benzene were synthesized from 2-hydroxy-3-methoxybenzaldehyde in eight steps. Compound 9h showed a potent inhibitory effect against P388 leukemia cells in vitro.
具有2,3 - 二乙酰氧基 - 4 - 甲氧基羰基 -(3',5'-二氧代 - N4'-取代哌嗪基甲基)苯结构的标题化合物由2 - 羟基 - 3 - 甲氧基苯甲醛经八步合成。化合物9h在体外对P388白血病细胞显示出强效抑制作用。