作者:Sydney Archer、Rabindra Rej
DOI:10.1021/jm00345a020
日期:1982.3
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
制备了卢卡酮的一组硝基和氨基衍生物,并测试了其抗肿瘤活性。1-氯-4-甲基-7-硝基噻吨酮和N,N-二乙基乙二胺的反应直接得到7-氨基类似物(11),并伴有7-氨基-1-氯-4-甲基噻吨酮。11的抗肿瘤活性不如卢坎酮和7-羟基葡吨酮。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,其200 mg / kg的T / C = 178。