Ho C H, Clark B R, Guerin M R, Barkenbus B D, Rao T K, Epler J L
Mutat Res. 1981 Oct;85(5):335-45. doi: 10.1016/0165-1161(81)90224-7.
Nitrogen-containing organic compounds from environmental sources are receiving increasing attention because of uniquely active mutagens which have been found in this class (Chrisp et al., 1978; Nagao and Sugimura, 1978: Guerin et al., 1980) Differences in mutagenic activities among the various organo-nitrogen compounds, i.e., pyrrole types, pyridine types and aniline types, have been noted consistently. Furthermore, differences among homologs of a particular compound type are often striking. Information in this paper engages the question of chemical structure/biological activity relationships. Activity data for several N-heterocyclic, nitro-, amino- (primary, secondary and tertiary), and amino-N-heterocyclic aromatic compounds are presented. The number of fused rings and the substituent type affect the mutagenic activities greatly. The trends observed are discussed generally with reference to molecular structural features.
由于在这类物质中发现了具有独特活性的诱变剂,来自环境源的含氮有机化合物受到越来越多的关注(克里斯普等人,1978年;长尾和杉村,1978年;格林等人,1980年)。一直有人指出,各种有机氮化合物(即吡咯类、吡啶类和苯胺类)的诱变活性存在差异。此外,特定化合物类型的同系物之间的差异往往也很显著。本文中的信息涉及化学结构/生物活性关系问题。文中给出了几种氮杂环、硝基、氨基(伯、仲和叔)以及氨基氮杂环芳香化合物的活性数据。稠环的数量和取代基类型对诱变活性有很大影响。结合分子结构特征对观察到的趋势进行了总体讨论。