Archer S, Rej R
J Med Chem. 1982 Mar;25(3):328-31. doi: 10.1021/jm00345a020.
A group of nitro and amino derivatives of lucanthone was prepared and tested for antitumor activity. Reaction of 1-chloro-4-methyl-7-nitrothioxanthenone and N,N-diethylethylenediamine gave the 7-amino analogue (11) directly, accompanied by 7-amino-1-chloro-4-methylthioxanthenone. The antitumor activity of 11 was inferior to that of lucanthone and 7-hydroxylucanthone. The most active compound in the series was the nitro compound 1. In the P-388 lymphocytic leukemia screen it showed a T/C = 178 at 200 mg/kg.
制备了一组卢卡酮的硝基和氨基衍生物,并对其抗肿瘤活性进行了测试。1-氯-4-甲基-7-硝基噻吨酮与N,N-二乙基乙二胺反应直接得到7-氨基类似物(11),同时伴有7-氨基-1-氯-4-甲基噻吨酮。11的抗肿瘤活性低于卢卡酮和7-羟基卢卡酮。该系列中活性最高的化合物是硝基化合物1。在P-388淋巴细胞白血病筛选中,它在200mg/kg时的T/C = 178。