Synthesis and biological activity of benzo[c]- and benzo[b]phenanthridinium salts
作者:V. I. Sladkov、V. A. Khokhlov、Yu. A. Ershova、V. A. Chernov、Yu. V. Khokhlova、A. F. Nanasyuk、N. N. Suvorov
DOI:10.1007/bf00758625
日期:1987.6
Benzo[c]phenanthridine alkaloids are known to possess antileukemic activity in mice against strains L-1210 and P-388 [5], The most active of the antileukemic quaternary benzo[c]phenanthridinium salts are nitidine, fagaronine, and fagaronine methyl ether [4, 6], Their use in medicine is however prevented by their high toxicity, For this reason, we have examined the effects of modifying fagaronine methyl
已知苯并 [c] 菲啶生物碱在小鼠体内对 L-1210 和 P-388 菌株具有抗白血病活性 [5],抗白血病季铵盐 [c] 菲啶盐中最具活性的是尼替丁、fagaronine 和 Fagaronine 甲醚 [ 4, 6],然而,它们的高毒性阻碍了它们在医学中的应用,因此,我们研究了修饰法加龙宁甲基醚对其抗肿瘤活性的影响。