Comparison of the QSAR models for toxicity and biodegradability of anilines and phenols

被引：50

作者：

Damborsky, J ^{[1
]}

Schultz, TW ^{[1
]}

机构：

[1] UNIV TENNESSEE, COLL VET MED, KNOXVILLE, TN 37901 USA

来源：

CHEMOSPHERE | 1997年 / 34卷 / 02期

关键词：

D O I：

10.1016/S0045-6535(96)00361-X

中图分类号：

X [环境科学、安全科学];

学科分类号：

08 ; 0830 ;

摘要：

Structure-activity models for toxicity and biodegradability of groups of m-anilines and p-phenols were developed and compared. Hydrophobicity was the most important property in determining toxicity. Whereas, electronic and steric properties were the more important in modeling biodegradation. (C) 1997 Elsevier Science Ltd.

引用

页码：429 / 446

页数：18

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