scholarly journals Adsorption Mechanism of Estrogens on Soil Studies Based on Density Functional Theory and Quantitative Structure-Activity Relationship Model

2015 ◽  
Vol 27 (4) ◽  
pp. 1199-1204
Author(s):  
Xiaoyu Liu ◽  
Shanshan Li ◽  
Yuhang Cai ◽  
Long Jiang ◽  
Nan Cheng ◽  
...  
Keyword(s):  
Density Functional Theory ◽  
Density Functional ◽  
Adsorption Mechanism ◽  
Quantitative Structure Activity Relationship ◽  
Structure Activity Relationship ◽  
Activity Relationship ◽  
Quantitative Structure ◽  
Functional Theory ◽  
Structure Activity ◽  
Relationship Model

scholarly journals Predictive Quantitative Structure–Activity Relationship Modeling of the Antifungal and Antibiotic Properties of Triazolothiadiazine Compounds

2020 ◽  
Vol 4 (1) ◽  
pp. 2
Author(s):  
Michael Appell ◽  
David L. Compton ◽  
Kervin O. Evans
Keyword(s):  
Density Functional Theory ◽  
Predictive Models ◽  
Density Functional ◽  
Quantitative Structure Activity Relationship ◽  
Structure Activity Relationship ◽  
Activity Relationship ◽  
Two Dimensional ◽  
Quantitative Structure ◽  
Functional Theory ◽  
Structure Activity

Predictive models were developed using two-dimensional quantitative structure activity relationship (QSAR) methods coupled with B3LYP/6-311+G** density functional theory modeling that describe the antimicrobial properties of twenty-four triazolothiadiazine compounds against Aspergillus niger, Aspergillus flavus and Penicillium sp., as well as the bacteria Staphylococcus aureus, Bacillus subtilis, Escherichia coli, and Pseudomonas aeruginosa. B3LYP/6-311+G** density functional theory calculations indicated the triazolothiadiazine derivatives possess only modest variation between the frontier orbital properties. Genetic function approximation (GFA) analysis identified the topological and density functional theory derived descriptors for antimicrobial models using a population of 200 models with one to three descriptors that were crossed for 10,000 generations. Two or three descriptor models provided validated predictive models for antifungal and antibiotic properties with R2 values between 0.725 and 0.768 and no outliers. The best models to describe antimicrobial activities include descriptors related to connectivity, electronegativity, polarizability, and van der Waals properties. The reported method provided robust two-dimensional QSAR models with topological and density functional theory descriptors that explain a variety of antifungal and antibiotic activities for structurally related heterocyclic compounds.

scholarly journals A Quantitative Structure – Activity Relationship Study on the Estrogen Activities of Bisphenol a Analogs using Computational Chemistry Methods and Multiple Linear Regression Technique

2018 ◽  
Vol 34 (3) ◽  
Author(s):  
Vu Van Dat ◽  
Le Kim Long ◽  
Doan Van Phuc ◽  
Nguyen Hoang Trang
Keyword(s):  
Density Functional Theory ◽  
Linear Regression ◽  
Bisphenol A ◽  
Multiple Linear Regression ◽  
Density Functional ◽  
Quantitative Structure Activity Relationship ◽  
Activity Relationship ◽  
Quantitative Structure ◽  
Functional Theory ◽  
Structure Activity

This article presents the results of the QSAR study of bisphenol A and its analogs. Molecular-chemical analysis of these substances is performed on base of the Density Functional Theory (DFT), using the function 6-31 + G *. The calculation of the characteristic parameters of the structure is given by optimizing molecular structures, vibrational frequencies, the molecular orbital energies with reasonable accuracy. The obtained quantum parameters and known observable activities are used as input data for constructing the QSAR model, using the classical data processing method in statistical mathematics - the multivariable linear regression. The constructed model QSAR has R2> 0,9; and . The statistical parameters show that the model, constructing by method of multiple linear regression using the parameters of quantum chemistry can be used as a predictive model of the activity of estrogens for unexplored derivatives and BPA analogs with moderate reliability. Keywords Bisphenol A, Estrogen, Density Functional Theory, M06 hybridmeta - GGA functional, Quantitative structure – activity relationship, Multiple linear regression References Rezg R, El-Fazaa S, Gharbi N, Mornagui B (March 2014). "Bisphenol A and human chronic diseases: Current evidences, possible mechanisms, and future perspectives".Environment International 2014, 64, 83–90. [2] Melzer D, Rice NE, Lewis C, Henley WE, Galloway TS (2010). Zhang, Baohong, ed."Association of Urinary Bisphenol a Concentration with Heart Disease: Evidence from NHANES 2003/06". PLoS ONE 5 (1). [3] Manikkam, M.; Tracey, R.; Guerrero-Bosagna, C.; Skinner, M. K. (January 24, 2013). "Plastics derived endocrine disruptors (BPA, DEHP and DBP) induce epigenetic transgenerational inheritance of obesity, reproductive disease and sperm epimutations".PLoS ONE 8 (1). 1–16. [4] D.R. Doerge, N.C. Twaddle, M. Vanlandingham, R.P. Brown, J.W. Fisher, Toxicol. Appl. Pharmacol. 2011, 255, 261.[5] Ho SM, Tang WY, Belmonte de Frausto J, Prins GS (2006). "Developmental exposure to estradiol and bisphenol A increases susceptibility to prostate carcinogenesis and epigenetically regulates phosphodiesterase type 4 variant 4". Cancer Res. 66 (11): 5624–32. [6] Johanna R. Rochester and Ashley L. Bolden (2015 Jul) “Bisphenol S and F: A Systematic Review and Comparison of the Hormonal Activity of Bisphenol A Substitutes”. Environ Health Perspect123(7):643-50.[7] Kelly, P. C., William, A. T., Thomas, E. W., QSAR models of thein vitro estrogen activity of bisphenol A analogs, QSAR Comb.Sci., 2003, 22: 78―88.[8]. Frisch, M. J. T., G. W. et al , Gaussian 09, Revision D.01. Gaussian, Inc., Wallingford CT, 2009.[9]. Zhao, Y.; Truhlar, D., The M06 suite of density functionals for main group thermochemistry, thermochemical kinetics, noncovalent interactions, excited states, and transition elements: two new functionals and systematic testing of four M06-class functionals and 12 other functionals. Theor Chem Account 2008,120 (1-3), 215-241.

Quantitative Structure-Activity Relationship of Morita-Baylis-Hillman Adducts with Leishmanicidal Activity

2011 ◽  
Vol 66 (3-4) ◽  
pp. 136-142
Author(s):  
Rodrigo Octavio M. A. de Souza ◽  
José C. Barros ◽  
Joaquim F. M. da Silva ◽  
Octavio A. C. Antunes
Keyword(s):  
Molecular Orbital ◽  
Quantitative Structure Activity Relationship ◽  
Structure Activity Relationship ◽  
Activity Relationship ◽  
Orbital Energy ◽  
Quantitative Structure ◽  
Leishmanicidal Activity ◽  
Structure Activity ◽  
Relationship Model ◽  
Relationship Of

A quantitative structure-activity relationship model for Morita-Baylis-Hillman adducts with leishmanicidal activities was developed which correlates molecular orbital energy and dipole with percentage in the promastigote stage

Sign in / Sign up

Export Citation Format

Share Document