Shirai T, Wang C Y
Mutat Res. 1980 Dec;79(4):345-50. doi: 10.1016/0165-1218(80)90159-7.
The nitrofurans, N-[4-(5-nitro-2-furyl)-2-thiazolyl]formamide (FANFT), N-[4-(5-nitro-2-furyl)-2-thiazolyl]acetamide (NFTA), 2-amino-4-(5-nitro-2-furyl)thiazole (ANFT), 2-methyl-4-(5-nitro-2-furyl)thiazole (MNFT), 2-(2-furyl)-3-(5-nitro-2-furyl)acrylamide (AF-2), nitrofurantoin, 5-nitro-2-furfurylidene diacetate and 5-nitro-2-furamidoxime were assayed for the enhancement of sister-chromatid exchange (SCE) in Chinese hamster ovary (CHO) cells and for the mutagenic activity in Salmonella typhimurium strain TA100. All of the nitrofurans significantly increased the frequency of SCE in CHO cells, and they were mutagenic for Salmonella. The increases in the frequencies of SCE were well correlated with the mutagenic activities in Salmonella.
对硝基呋喃类化合物,即N-[4-(5-硝基-2-呋喃基)-2-噻唑基]甲酰胺(FANFT)、N-[4-(5-硝基-2-呋喃基)-2-噻唑基]乙酰胺(NFTA)、2-氨基-4-(5-硝基-2-呋喃基)噻唑(ANFT)、2-甲基-4-(5-硝基-2-呋喃基)噻唑(MNFT)、2-(2-呋喃基)-3-(5-硝基-2-呋喃基)丙烯酰胺(AF-2)、呋喃妥因、5-硝基-2-糠叉二乙酸酯和5-硝基-2-呋喃甲肟进行了检测,以观察其对中国仓鼠卵巢(CHO)细胞姐妹染色单体交换(SCE)的增强作用以及对鼠伤寒沙门氏菌TA100菌株的致突变活性。所有硝基呋喃类化合物均显著增加了CHO细胞中SCE的频率,并且它们对沙门氏菌具有致突变性。SCE频率的增加与沙门氏菌中的致突变活性密切相关。