EventsMOL2NET'16, Conference on Molecular, Biomed., Comput. & Network Science and Engineering, 2nd ed.
Published
This submission belongs to the session 02. CHEMBIOMOL-02: Chem. Biol. & Med. Chem. Workshop, Rostock, Germany-Bilbao, Spain-Galveston, Texas, USA, 2016 of the event MOL2NET'16, Conference on Molecular, Biomed., Comput. & Network Science and Engineering, 2nd ed.
Published date
18 Jan, 2017
Citation
Juan Alberto Castillo-Garit, Yudith Cañizares-Carmenate, Karel Mena-Ulecia, Yunier Perera-Sardiña, Francisco Torrens, Multiple Linear Regression Model of Thermolysin Inhibitors, in Proceedings of MOL2NET'16, Conference on Molecular, Biomed., Comput. & Network Science and Engineering, 2nd ed., 15 October–20 October 2022, MDPI: Basel, Switzerland, doi: 10.3390/mol2net-02-03872
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Multiple Linear Regression Model of Thermolysin Inhibitors

Karel Mena-Ulecia 3
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1. Unidad de Toxicología Experimental, Universidad de Ciencias Médicas de Villa Clara, Santa Clara, Villa Clara, Cuba. CP: 50200, Cuba
2. Bioinformatic Research in Systems & Computer Engineering, Carleton University, Ottawa, Canada
3. Centro Interdisciplinario de Neurociencia de Valparaiso, Facultad de Ciencias, Universidad de Valparaiso, Valparaiso, Chile
4. Doctorado en Fisicoquimica Molecular, Center of Applied Nanosciences (CENAP), Universidad Andres Bello, Ave. Republica 275, Santiago, Chile
5. Institut Universitari de Ciència Molecular, Universitat de València, Edifici d'Instituts de Paterna, P. O. Box 22085, 46071 Valencia, Spain
Abstract

Thermolysin is a bacterial proteolytic enzyme, considered by many authors as a pharmacological and biological model of other mammalian enzymes, with similar structural characteristics, such as Angiotensin Converting Enzyme and Neutral Endopeptidase. Inhibitors of these enzymes are considered therapeutic targets for common diseases, such as hypertension and heart failure. In this report, a mathematical model of Multiple Linear Regression, for ordinary least squares, and genetic algorithm, for selection of variables, are developed and implemented in QSARINS software, with appropriate parameters for its fitting. The model is extensively validated according to OECD standards, so that its robustness, stability, low correlation of descriptors and good predictive power are proven. In addition, it is found that the model fit is not the product of a random correlation. Two possible outliers are identified in the model application domain but, in a molecular docking study, they show good activity, so we decide to keep both in our database. The obtained model can be used for the virtual screening of compounds, in order to identify new active molecules.

Keywords
Antihypertensive
Docking
Multiple Linear Regression
QSARINS
Thermolysin
Poster
Thermolysin.pdf
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