Synthesis and Antitumor Activity of Fused Quinoline Derivatives. III. Novel N-Glycosylaminoindolo(3,2-b)quinolines.
作者:Yasuo TAKEUCHI、Ming-rong CHANG、Kuniko HASHIGAKI、Tazuko TASHIRO、Takashi TSURUO、Shigeru TSUKAGOSHI、Masatoshi YAMATO
DOI:10.1248/cpb.40.1481
日期:——
Novel indolo[3,2-b]quinolines (1b-k), having a nitro, amino, acetamido, methanesulfonamido, or glycosylamino group at the 2, 7, or 8-position, were prepared and their antitumor activities against P388 leukemia in mice were examined. The 7-galactopyranosylamino derivative (1g) showed the most potent activity (optimal dose = 25 mg/kg, T/C greater than 333%, cure rate 5/6).
制备了在2、7或8位具有硝基,氨基,乙酰氨基,甲磺酰胺基或糖基氨基的新型吲哚并[3,2-b]喹啉(1b-k),并在体外对P388白血病具有抗肿瘤活性。检查小鼠。7-galactopyranosylamino衍生物(1g)表现出最强的活性(最佳剂量= 25 mg / kg,T / C大于333%,治愈率5/6)。