Lessigiarska I, Wortha A P, Sokull-Klüttgen B, Jeram S, Dearden J C, Netzeva T I, Cronin M T D
European Centre for the Validation of Alternative Methods, Institute for Health and Consumer Protection, Joint Research Centre, European Commission, 21020 Ispra (VA), Italy.
SAR QSAR Environ Res. 2004 Oct-Dec;15(5-6):413-31. doi: 10.1080/10629360412331297416.
A large data set containing values for fish, algae and Daphnia toxicity for more than 2000 chemicals and mixtures was investigated. The data set was taken from the New Chemicals Data Base of the European Union [hosted by the European Chemicals Bureau, Joint Research Centre, European Commission (http://ecb.jrc.it)]. The data are submitted by industry, according to the requirements of EU Council Directive 67/548/EEC as amended for the seventh time by EU Council Directive 92/32/EEC. The toxicities of neutral chemicals, salts, metal complexes, as well as chemical mixtures were extracted. A baseline effect was demonstrated by chemicals known to act by a narcotic mechanism of action, i.e., a relationship was observed between the toxicity and the logarithm of the octanol-water partition coefficient (log P). However, the prediction of the toxicity of more reactive chemicals was found to require the use of additional descriptors.
对一个包含2000多种化学品和混合物的鱼类、藻类和水蚤毒性值的大型数据集进行了研究。该数据集取自欧盟的新化学品数据库[由欧盟委员会联合研究中心欧洲化学品局托管(http://ecb.jrc.it)]。这些数据是行业根据欧盟理事会指令67/548/EEC的要求提交的,该指令已被欧盟理事会指令92/32/EEC第七次修订。提取了中性化学品、盐、金属络合物以及化学混合物的毒性。已知通过麻醉作用机制起作用的化学品显示出基线效应,即观察到毒性与辛醇-水分配系数的对数(log P)之间存在关系。然而,发现预测反应性更强的化学品的毒性需要使用其他描述符。