Mutagenic activity of 6-aminoquinoxalines in Salmonella typhimurium

Yoshiyasu Terao, Issei Achiwa, Satoru Kishino, Yasufumi Matsumura, Tatsushi Shiozawa, Hidetsuru Matsushita
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Abstract

Mutagenicity of 6-aminoquinoxaline derivatives was tested with Salmonella typhimurium strains Ta98 and TA100 in the presence and absence of S9 mix from the viewpoint that the 6-aminoquinoxaline skeleton is a common unit of mutagenic imidazoquinoxalines. We tested nine compounds: 5-methyl-6-methylaminoquinoxaline (1), 3,5-dimethyl-6-methylaminoquinoxaline (2), 2,5-dimethyl-6-metnylaminoquinoxaline (3), 6-methylamino-2,3,5-trimethylquinoxaline (4), 2,3-diethyl-5-methyl-6-methylaminoquinoxaline (5), 5-methyl-6-methylamino 3-phenylquinoxaline (6), 6-amino-2,3,5-trimethylquinoxaline (7), 6-dimethylamino-2,3-5-trimethylaminoquinoxaline (8), 6-amino-2,3-dimethylquinoxaline (9). These compounds showed the mutagenic activity for both TA98 and TA100 in the presence of S9 mix, where they were more sensitive for TA100 strain. Methyl groups at the 2, 3 and/or 5 positions increased the potency of mutagenicity (1 < 2 < 3 ⪡ 4, 9 < 7). However, ethyl groups at the 2 and 3 positions lowered the mutagenicity of the methyl substitute but elevated it of the parental compound (1 < 5 < 4). A methyl group at the N6 position decreased the mutagenicity (7 > 4 > 8).

6-氨基喹啉类对鼠伤寒沙门氏菌的致突变活性研究
从6-氨基喹诺啉骨架是致突变性咪唑喹诺啉类化合物的共同单位的观点出发,用鼠伤寒沙门氏菌Ta98和TA100菌株在有无S9混合物的情况下对6-氨基喹诺啉衍生物进行了致突变性试验。我们测试了九种化合物:5-dimethyl-6-methylaminoquinoxaline 5-methyl-6-methylaminoquinoxaline(1), 3日(2),2,5-dimethyl-6-metnylaminoquinoxaline (3), 6-methylamino-2, 3, 5-trimethylquinoxaline (4), 2, 3-diethyl-5-methyl-6-methylaminoquinoxaline (5), 5-methyl-6-methylamino 3-phenylquinoxaline (6), 6-amino-2, 3, 5-trimethylquinoxaline (7), 6-dimethylamino-2, 3-5-trimethylaminoquinoxaline (8), 6-amino-2, 3-dimethylquinoxaline(9)。这些化合物显示了诱变活性对TA98和TA100的S9混合,它们对TA100菌株更敏感。2、3和/或5位的甲基增加了致突变性的效力(1 <2 & lt;3⪡4,9 <7).然而,2和3位的乙基降低了甲基替代品的致突变性,但提高了亲本化合物的致突变性(1 <5 & lt;4). N6位置的甲基降低了致突变性(7 >4比;8).
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