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Mutagenic activity of 6-aminoquinoxalines in Salmonella typhimurium.

机译:鼠伤寒沙门氏菌中6-氨基喹喔啉的诱变活性。

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摘要

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-methylaminoquinoxaline (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).
机译:从6-氨基喹喔啉骨架是致突变的咪唑并喹喔啉的常见单元的观点出发,在有和没有S9混合物的情况下,用鼠伤寒沙门氏菌菌株TA98和TA100测试了6-氨基喹喔啉衍生物的致突变性。我们测试了9种化合物:5-甲基-6-甲基氨基喹喔啉(1),3,5-二甲基-6-甲基氨基喹喔啉(2),2,5-二甲基-6-甲基氨基喹喔啉(3),6-甲基氨基-2,3, 5-三甲基喹喔啉(4),2,3-二乙基-5-甲基-6-甲基氨基喹喔啉(5),5-甲基-6-甲基氨基3-苯基喹喔啉(6),6-氨基-2,3,5-三甲基喹喔啉( 7),6-二甲基氨基-2,3,5-三甲基氨基喹喔啉(8),6-氨基-2,3-二甲基喹喔啉(9)。这些化合物在存在S9混合物的情况下对TA98和TA100均显示出诱变活性,其中它们对TA100菌株更敏感。在2、3和/或5位的甲基提高了诱变能力(1 <2 <3 4,9 <7)。但是,在2和3位的乙基降低了甲基取代基的诱变性,但提高了母体化合物的诱变性(1 <5 <4)。 N6位的甲基会降低诱变性(7> 4> 8)。

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