Kortselius M J
Mutat Res. 1978 Jul;57(3):297-305. doi: 10.1016/0027-5107(78)90214-2.
BCNU and 10 related chloroethylnitrosoureas were tested for their ability to induce sex-linked recessive lethals in Drosophila spermatozoa. All chloroethylnitrosoureas tested were potent mutagens. Among the substances with one chloroethylnitrosourea group, chlorozotocin, BCNU and methanesulfonyloxyethyl chloroethylnitrosourea exhibited the strongest mutagenic effects. Two hydroxyalkyl chloroethylnitrosoureas behaved as potent mutagens too, although the mutation frequencies obtained were one order of magnitude lower relative to the other substances. Among the compounds with two chloroethylnitrosourea groups, bisCNU-ethane and bisCNU-diphenylmethane were most active. When the interconnecting polymethylene chain was elongated from 2 methylene groups (bisCNU-ethane) to 6 methylene groups (bisCNU-hexane), the mutagenic activity decreased by a factor of 2. The mutagenic activity of polymethylene bischloroethylnitrosoureas with connecting chains of intermediate length was not different from bisCNU-hexane. Differences in mutagenic activity were supposed to reflect different concentrations reaching the target cells, possibly in part as a result of differences in transportability of the substances.
对卡莫司汀(BCNU)和10种相关的氯乙基亚硝基脲进行了测试,以检验它们在果蝇精子中诱发性连锁隐性致死突变的能力。所有测试的氯乙基亚硝基脲都是强效诱变剂。在含有一个氯乙基亚硝基脲基团的物质中,氯脲霉素、卡莫司汀和甲磺酰氧基乙基氯乙基亚硝基脲表现出最强的诱变作用。两种羟烷基氯乙基亚硝基脲也表现为强效诱变剂,尽管相对于其他物质,获得的突变频率低一个数量级。在含有两个氯乙基亚硝基脲基团的化合物中,双(氯乙基亚硝基脲)乙烷和双(氯乙基亚硝基脲)二苯甲烷最为活跃。当连接的聚亚甲基链从2个亚甲基(双(氯乙基亚硝基脲)乙烷)延长到6个亚甲基(双(氯乙基亚硝基脲)己烷)时,诱变活性降低了2倍。具有中间长度连接链的聚亚甲基双氯乙基亚硝基脲的诱变活性与双(氯乙基亚硝基脲)己烷没有差异。诱变活性的差异被认为反映了到达靶细胞的不同浓度,这可能部分是由于物质转运能力的差异所致。