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Toxicity of some prevalent organic chemicals to tadpoles and comparison with toxicity to fish based on mode of toxic action

机译:某些常见有机化学物质对t的毒性,并根据毒性作用方式与对鱼类的毒性进行比较

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Although mode of action (MOA) plays a key role in the understanding of the toxic mechanism of chemicals, the MOAs of class-based compounds to tadpoles have not been investigated. To explore the MOAs, acute toxicity (expressed as log 1/LC50) to Rana chensinensis tadpoles were determined and molecular descriptors were calculated. Quantitative structure-activity relationship (QSAR) showed that toxicity to tadpoles is closely related to the chemical octanol/water partition coefficient (log K-ow), energy of the lowest unoccupied molecular orbital (E-L(UMO)), and number of hydrogen bond donors and acceptors (NHDA), representing the bio-uptake potential in tadpoles, the electrophilicity and hydrogen bonding capacity with target site(s), respectively. Comparison of the toxicity values between tadpoles and fish revealed that there were no significant differences for the overlapping compounds (average residual = 0.29 between tadpole and fish toxicity) with P values of interspecies correlation substantially less than 0.001. Classification of MOAs for the class-based compounds based on the excess toxicity calculated from toxicity ratio suggested that baseline, less inert compounds and some reactive or specifically-acting compounds share same MOAs between tadpoles and fish. Fish and tadpoles can serve as surrogates for each other in the safety evaluation of organic pollutants.
机译:尽管作用方式(MOA)在了解化学物质的毒性机理中起着关键作用,但尚未研究基于类化合物的t的MOA。为了研究MOA,确定了对林蛙t的急性毒性(表示为log 1 / LC50),并计算了分子描述子。定量构效关系(QSAR)表明,对toxicity的毒性与化学辛醇/水分配系数(log K-ow),最低未占据分子轨道的能量(EL(UMO))和氢键数密切相关供体和受体(NHDA),分别代表t的生物吸收潜力,亲电性和与目标部位的氢键合能力。 t和鱼的毒性值的比较表明,重叠的化合物之间没有显着差异(t和鱼的毒性之间的平均残留= 0.29),种间相关性的P值小于0.001。基于毒性比率计算出的过量毒性,对基于类别的化合物的MOA进行分类表明,基线,惰性较小的化合物以及某些具有反应性或特异作用的化合物在t和鱼类之间共享相同的MOA。鱼和t在有机污染物的安全性评估中可以互相替代。

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