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• W2015165786 abstract "By using multi-block partial least-squares (MBPLS) method, quantitative structure-activity relationship (QSAR) between 35 organophosphate compounds (OP) and their 24h acute toxicities towards the housefly (Musca nebulo L.) was built on the molecular interaction fields (MIF) descriptors, which were obtained with O, N and DRY as probes, and then normalised with block unscaled weights (BUW) technique. The best QSAR model had 8 principal components, with the coefficient of determination R(2)=0.995 and that of leave-one-out cross-validation Q(2)=0.865, and the corresponding standard deviation of error 0.076 and 0.361, respectively. Block importance in the prediction (BIP) for O, N and DRY probe were 1.030, 0.962 and 1.007, respectively. Contour map of variable coefficients showed that hydrogen bonding between the O atom in PO and the NH groups in acetylcholinesterase (AChE) played an important role in the interaction between OP and AChE. Meanwhile, the hydrophobicity of OP also had significant contribution. QSAR based on the MIF descriptors could be a potential means to interpret the mechanisms of ligand-receptor interaction when the receptor was well known." @default.
• W2015165786 created "2016-06-24" @default.
• W2015165786 creator A5015878848 @default.
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• W2015165786 date "2013-03-01" @default.
• W2015165786 modified "2023-10-16" @default.
• W2015165786 title "Quantitative structure–activity relationship of organophosphate compounds based on molecular interaction fields descriptors" @default.
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• W2015165786 doi "https://doi.org/10.1016/j.etap.2012.11.018" @default.
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