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本文引用的文献

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2
Assessing the toxic effects of ethylene glycol ethers using Quantitative Structure Toxicity Relationship models.采用定量构效关系模型评估乙二醇醚的毒性效应。
Toxicol Appl Pharmacol. 2011 Jul 15;254(2):198-205. doi: 10.1016/j.taap.2010.10.024. Epub 2010 Oct 27.
3
Decrease of intracellular pH as possible mechanism of embryotoxicity of glycol ether alkoxyacetic acid metabolites.细胞内 pH 值降低可能是乙二醇醚单乙氧基乙酸代谢物胚胎毒性的机制。
Toxicol Appl Pharmacol. 2010 Jun 1;245(2):236-43. doi: 10.1016/j.taap.2010.03.005. Epub 2010 Mar 11.
4
Chemical risk assessment and uncertainty associated with extrapolation across exposure duration.化学风险评估及与跨接触时间外推相关的不确定性
Regul Toxicol Pharmacol. 2010 Jun;57(1):18-23. doi: 10.1016/j.yrtph.2009.11.007. Epub 2009 Nov 26.
5
Molecular dynamics study of zinc binding to cysteines in a peptide mimic of the alcohol dehydrogenase structural zinc site.锌与醇脱氢酶结构锌位点肽模拟物中半胱氨酸结合的分子动力学研究。
Phys Chem Chem Phys. 2009 Feb 14;11(6):975-83. doi: 10.1039/b815482a. Epub 2008 Dec 12.
6
Development of quantitative structure-activity relationship (QSAR) models to predict the carcinogenic potency of chemicals I. Alternative toxicity measures as an estimator of carcinogenic potency.用于预测化学物质致癌潜力的定量构效关系(QSAR)模型的开发 I. 作为致癌潜力估计值的替代毒性指标
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7
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8
The ToxCast program for prioritizing toxicity testing of environmental chemicals.用于对环境化学品毒性测试进行优先级排序的ToxCast计划。
Toxicol Sci. 2007 Jan;95(1):5-12. doi: 10.1093/toxsci/kfl103. Epub 2006 Sep 8.
9
Relating protein motion to catalysis.将蛋白质运动与催化作用联系起来。
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10
Butoxyacetic acid-induced hemolysis of rat red blood cells: effect of external osmolarity and cations.丁氧基乙酸诱导的大鼠红细胞溶血:细胞外渗透压和阳离子的影响
Toxicol Lett. 2005 Mar 28;156(1):81-93. doi: 10.1016/j.toxlet.2003.09.020.

烷氧基乙醇混合物的联合毒性:计算应用的贡献。

Joint toxicity of alkoxyethanol mixtures: contribution of in silico applications.

机构信息

Agency for Toxic Substances and Disease Registry, US Department of Health and Human Services, Atlanta, GA, USA.

出版信息

Regul Toxicol Pharmacol. 2012 Oct;64(1):134-42. doi: 10.1016/j.yrtph.2012.06.008. Epub 2012 Jun 28.

DOI:10.1016/j.yrtph.2012.06.008
PMID:22749914
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5599109/
Abstract

Exposure to chemicals occurs often as mixtures. Presented in this paper is information on alkoxyethanols and the impact they might have on human health in combination with some commonly found aliphatic and aromatic compounds. Our studies to evaluate the joint toxicity of these chemicals among themselves and in combination with other chemicals reveal a variety of possible outcomes depending on the exposure scenario. The interactions are predominantly based on metabolic pathways and are common among several solvents and organic compounds. Quantitative structure activity relationship (QSAR) analysis can be used with high confidence to identify chemicals that will interact to influence overall joint toxicity. Potential human exposure to a combination of alkoxyethanol, toluene and substituted benzenes may increase reproductive and developmental disease conditions. Inheritable gene alterations result in changes in the enzyme function in different subpopulations causing variations in quantity and/or quality of particular isoenzymes. These changes are responsible for differential metabolism of chemicals in species, genders, and life stages and are often the basis of a population's susceptibility. Unique genotypes introduced as a function of migration can alter the genetic makeup of any given population. Hence special consideration should be given to susceptible populations while conducting chemical health risk assessments.

摘要

接触化学物质通常是混合物。本文介绍了烷氧基乙醇的信息,以及它们与一些常见的脂肪族和芳香族化合物结合时可能对人类健康造成的影响。我们的研究评估了这些化学物质之间以及与其他化学物质联合的联合毒性,结果表明根据暴露情况,可能会产生各种不同的结果。这些相互作用主要基于代谢途径,在几种溶剂和有机化合物中很常见。定量构效关系(QSAR)分析可用于高度置信地识别可能相互作用影响整体联合毒性的化学物质。潜在的人类接触烷氧基乙醇、甲苯和取代苯的混合物可能会增加生殖和发育疾病的发生。可遗传的基因突变导致不同亚群中酶功能的改变,从而导致特定同工酶的数量和/或质量发生变化。这些变化负责物种、性别和生命阶段中化学物质的差异代谢,通常是种群易感性的基础。由于迁移而引入的独特基因型会改变任何特定种群的遗传组成。因此,在进行化学健康风险评估时,应特别关注易感人群。