Quantitative structure-analysis relationships QSARs

Furthermore, QSPR models for the prediction of free-energy based properties that are based on multilinear regression analysis are often referred to as LFER models, especially, in the wide field of quantitative structure-activity relationships (QSAR). 

Gao H, Williams C, Labute P, Bajorath J. Binary quantitative structure-activity relationship (QSAR) analysis of estrogen receptor ligands. / Chem Inf Comput Sci 1999 39 164-8. 

Hansch and Verma contribute to the quantitative structure-activity relationship (QSAR) analysis of heterocyclic topoisomerase I and II inhibitors. These inhibitors, known to inhibit either enzyme, act as antitumor agents and are currently used in chemotherapy and in clinical trials. 

QEKIRVRLSA antimicrobial peptide, 26 799-800 Qiana, 19 764 QikProp, 6 18 Qinghai Lake, 5 784 Q parameter, impeller, 16 676 QSAR analysis, 10 327t, 328-329. See also Quantitative structure—activity relationship (QSAR) studies 3D QSAR models... 

The synthesis and antibacterial properties of norfloxacin (2a) were described in 1980 [65]. In this key paper in the evolution of quinolone antibacterial agents, a series of 6,7,8-polysubstituted-l-ethyl-l,4-dihydro-4-oxoquinoline-3-carb-oxylic acids (13) was synthesized, employing previously developed quantitative structure-activity relationships (QSAR) for the corresponding 6-, 7- and 8-monosubstituted derivatives versus Escherichia coli. The QSAR analysis... 

Crebelli, R., Andreoli, C., Carere, A., Conti, G., Conti, L., Cotta-Ramusino, M., Benigni, R. The induction of mitotic chromosome malsegregation in Aspergillus nidulans. Quantitative structure activity relationship (QSAR) analysis with chlorinated aliphatic hydrocarbons. Mutat. Res. 1992, 266, 117-134. 

KARMA is an interactive computer assisted drug design tool that incorporates quantitative structure-activity relationships (QSAR), conformational analysis, and three-dimensional graphics. It represents a novel approach to receptor mapping analysis when the x-ray structure of the receptor site is not known, karma utilizes real time interactive three-dimensional color computer graphics combined with numerical computations and symbolic manipulation techniques from the field of artificial intelligence. 

Lesigiarska, I., Pajeva, I., and Yanev, S. (2002) Quantitative structure-activity relationship (QSAR) and three-dimensional QSAR analysis of a series of xanthates as inhibitors and inactivators of cytochrome P450 2B1. Xenobiotica 32, 1063-1077. 

It is important to consider the molecular interactions in liquids that are responsible for their physicochemical properties (such as boiling point, melting point, heat of vaporization, surface tension, etc.), which enables one to both describe and relate the different properties of matter in a more clear manner (both qualitatively and quantitatively). These ideas form the basis for quantitative structure activity relationship (QSAR Birdi, 2002). This approach toward analysis and application is becoming more common due to the enormous help available from computers. 

Drug binding is enhanced by hydrophobicity in that portion of the drug that binds to the pocket toe. Quantitative structure-activity relationship (QSAR) analysis of these compounds have consistently shown that the most predictive parameter of antiviral activity is a measure of hydrophobicity, the octanol water partition coefficient (logP) [80,82,85]. These studies have also consistently shown that there is no apparent correlation between electrostatic potential or dipole moment and potency. 

An instructive quantitative structure-activity relationship (QSAR) analysis carried out on published data about a large set of cationic lipids, including both successful and unsuccessful compounds, permitted to delineation of a high-efficiency region... 

Mon J. Flury M. and Harsh J.B. (2006). A quantitative structure-activity relationship (QSAR) analysis of triarylmethane dye tracers. Journal of Hydrology, 316(1-4), 84-97. 

Systematic studies of the effects of structure on the biological activities of organic compounds and the analysis of the results are comprised in the term Quantitative Structure-Activity Relationships (QSAR). Many of the treatments employed in the correlation analysis of data in this field closely resemble those used for linear free-energy relationships, e.g. the Hammett equation and extensions thereof, and so the study of the biological properties of organic compounds is often regarded as a part of physical organic chemistry. In recent years, some historical study of work in... 

Debnath, A.K., Hansch, C., Kim, K.H., and Martin, Y.C., Mechanistic interpretation of the genotoxicity of nitrofurans (antibacterial agents) using quantitative structure-activity relationships (QSAR) and comparative molecular field analysis (CoMFA), J. Med. Chem., 36, 1009-1116, 1993. 

Woo, Y.T. and Lai, D.Y., Mechanisms of action of chemical carcinogens and their role in structure-activity relationships (SARs) analysis and risk assessment in Quantitative Structure-Activity Relationship (QSAR) Models of Mutagens and Carcinogens, Benigni, R., Ed., CRC Press, Boca Raton, FL 2003, pp. 41-80. 

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