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苯并呋喃和萘并呋喃在沙门氏菌/微粒体试验中的致突变活性:2-硝基-7-甲氧基-萘并[2,1-b]呋喃(R7000),一种新型高效致突变剂。

Mutagenic activity of benzofurans and naphthofurans in the Salmonella/microsome assay: 2-nitro-7-methoxy-naphtho[2,1-b]furan (R7000), a new highly potent mutagenic agent.

作者信息

Weill-Thevenet N, Buisson J P, Royer R, Hofnung M

出版信息

Mutat Res. 1981 Apr;88(4):355-62. doi: 10.1016/0165-1218(81)90027-6.

Abstract

A series of benzofurans and naphthofurans was examined through the Salmonella/microsome assay. (i) With one possible exception, only 2-nitro derivatives give a mutagenic response. However, it appears that the mutagenic potency depends notably on the nature and the position of the other substituents in the molecule. (ii) The mutagenic response occurs in strains TA1537, TA1538, TA98 and TA100 but not in strain TA1535. Reversion of the missense mutation of TA1535 is thus induced only in presence of the plasmid pKM101. (iii) This mutagenic response is at least partially dependent on the bacterial nitroreductase activities and is usually lower in presence of activating mixture from rat liver. (iv) One of the compounds tested, 2-nitro-7-methoxynaphtho[2,1-b]furan (R7000), may be the most potent mutagen examined so far in the Salmonella/microsome assay. It yields about 200 000 revertants/nanomole on strain TA100 in the standard plate test. The relation between structure, mutagenic potency and other biological activities of the compounds are briefly discussed.

摘要

通过沙门氏菌/微粒体试验对一系列苯并呋喃和萘并呋喃进行了检测。(i) 除一种可能的例外情况外,只有2-硝基衍生物会产生诱变反应。然而,诱变效力似乎明显取决于分子中其他取代基的性质和位置。(ii) 诱变反应发生在TA1537、TA1538、TA98和TA100菌株中,但在TA1535菌株中不发生。因此,只有在质粒pKM101存在的情况下,TA1535的错义突变才会发生回复突变。(iii) 这种诱变反应至少部分依赖于细菌硝基还原酶的活性,并且在存在大鼠肝脏激活混合物的情况下通常较低。(iv) 所测试的化合物之一,2-硝基-7-甲氧基萘并[2,1-b]呋喃(R7000),可能是迄今为止在沙门氏菌/微粒体试验中检测到的最有效的诱变剂。在标准平板试验中,它在TA100菌株上产生约200 000个回复突变体/纳摩尔。简要讨论了这些化合物的结构、诱变效力和其他生物活性之间的关系。

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