el-Hamouly W, Pica-Mattoccia L, Cioli D, Schwartz H M, Archer S
Cogswell Laboratories, Chemistry Department, Rensselaer Polytechnic Institute, Troy, New York 12180-3590.
J Med Chem. 1988 Aug;31(8):1629-31. doi: 10.1021/jm00403a024.
On the basis of the remarkable biological similarities between hycanthone and oxamniquine and as a sequel to our finding that some esters of hycanthone are active against hycanthone-resistant schistosomes, we prepared oxamniquine acetate, oxamniquine N-methylcarbamate, and four substituted phenylsulfonohydrazones of oxamniquine aldehyde. These compounds were tested for their effect on survival of and on [3H]uridine incorporation into hycanthone-sensitive and -resistant Schistosoma mansoni. All of these derivatives were effective to a greater or lesser degree in killing worms and in inhibiting [3H]uridine incorporation in the sensitive strain, but none was effective in the resistant strain.
基于海恩酮和奥沙尼喹之间显著的生物学相似性,以及我们发现海恩酮的某些酯对耐海恩酮的血吸虫具有活性这一结果,我们制备了醋酸奥沙尼喹、氨基甲酸N-甲酯奥沙尼喹以及奥沙尼喹醛的四种取代苯磺酰腙。测试了这些化合物对海恩酮敏感和耐药曼氏血吸虫存活以及对[³H]尿苷掺入的影响。所有这些衍生物在杀死敏感株的虫体以及抑制[³H]尿苷掺入方面都有不同程度的效果,但对耐药株均无效。