Golovinsky E, Norpoth K, Stankevich E, Mohtashamipur E
Cancer Lett. 1983 May;19(1):67-72. doi: 10.1016/0304-3835(83)90137-4.
Five newly synthesized hydrazides: L-aspartic acid dihydrazide, DL-ureido-succinic acid dihydrazide, DL-dihydroorotic acid hydrazide, orotic acid hydrazide, and 2,2'-anhydro-1-(beta-D-arabinofuranosyl)-orotic acid hydrazide were tested for mutagenicity in the Ames test. All these hydrazides except DL-ureidosuccinic acid dihydrazide were found to be non-mutagenic. The mutagenic activities of the latter compound which causes base-pair substitution was decreased in the presence of metabolic activator.
L-天冬氨酸二酰肼、DL-脲基琥珀酸二酰肼、DL-二氢乳清酸酰肼、乳清酸酰肼和2,2'-脱水-1-(β-D-阿拉伯呋喃糖基)乳清酸酰肼进行了艾姆斯试验以检测其致突变性。发现除DL-脲基琥珀酸二酰肼外,所有这些酰肼均无致突变性。后一种引起碱基对置换的化合物在代谢激活剂存在下致突变活性降低。