法律 发表于 2025-3-23 12:26:53
http://reply.papertrans.cn/79/7801/780021/780021_11.pngAdulterate 发表于 2025-3-23 17:01:59
Relationship Between Toxicity and Bioconcentration for Some Organic Chemicals. II. Application of ter, one-compartment model assumptions, to estimate toxicant kinetic parameters. This was accomplished via non-linear curve fitting to time-toxicity data from typical LC50 toxicity tests. Preliminary results for a limited data set are presented. It appears that:Insufficient 发表于 2025-3-23 20:49:01
http://reply.papertrans.cn/79/7801/780021/780021_13.png信任 发表于 2025-3-24 01:41:59
http://image.papertrans.cn/q/image/780021.jpg有害 发表于 2025-3-24 05:26:41
http://reply.papertrans.cn/79/7801/780021/780021_15.png忍受 发表于 2025-3-24 09:33:07
http://reply.papertrans.cn/79/7801/780021/780021_16.pngHAUNT 发表于 2025-3-24 13:44:33
http://reply.papertrans.cn/79/7801/780021/780021_17.png宽容 发表于 2025-3-24 17:43:51
QSAR of Acute Toxicity of 1,4-Di-Substituted Benzene Derivatives and Relationships with the Acute Ttoxicities of the corresponding mono-substituted benzene derivatives of the same general formula with R = H, both for the entire set (r. = 0.33; n = 133) and each of the subsets, particularly so for R = CI (r. = 0.71; n = 35). After elimination of highly toxic compounds, the remaining set of 105 di-为现场 发表于 2025-3-24 21:33:21
Quantitative Structure-Activity Studies of Di-and Triorganotin Compounds,es linearly only to a certain point before declining. Triorganotin compounds approximately the size (total surface area) of tricyclohexyltin are at or perhaps slightly above such a maximum. These studies of di- and triorganotin compounds suggest that such approaches are highly promising tools for thHost142 发表于 2025-3-24 23:41:59
Comparison of Fish Toxicity Screening Data and QSAR Predictions for 48 Aniline Derivatives,e equilibrium, limiting water solubility, or a combination of both of these factors. Several compounds exhibited toxicity at concentrations significantly below those predicted; these results were interpreted in terms of electrophile or proelectrophile mechanisms.