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https://open.uns.ac.rs/handle/123456789/17705
Title: | Chemometrics approach based on chromatographic behavior, in silico characterization and molecular docking study of steroid analogs with biomedical importance | Authors: | Karadžić Banjac, Milica Jevrić, Lidija Mandić, Anamarija Markov, Siniša Podunavac-Kuzmanović, Sanja Kovačević, Strahinja Nikolić (Gaković), Andrea Oklješa, Aleksandar Sakač, Marija Penov-Gaši, Katarina |
Issue Date: | 15-Jul-2017 | Publisher: | Elsevier | Journal: | European Journal of Pharmaceutical Sciences | Abstract: | © 2017 Elsevier B.V. Physicochemical characterization of steroid analogs (triazole, tetrazole, toluenesulfonylhydrazide, nitrile, dinitrile and dione) is considered to be a very important step in further drug selection. This study applies to the determination of lipophilicity of previously synthesized steroid derivatives using reversed-phase high-performance liquid chromatography (RP HPLC). Chemometric aspect of chromatographic lipophilicity is given throughout multiple linear regression (MLR) quantitative structure-retention relationships (QSRR) approach. Minimal inhibitory concentration (MIC) is determined for two steroid derivatives possessing antimicrobial activity against Staphylococcus aureus. Molecular docking study was performed in order to identify the compound with the most promising potential as human cytochrome P450 CYP17A1inhibitor. Identified 3β-hydroxyandrost-5-eno[16,17-d]-1,2,3-triazole (I.2.) could be recommended for further trials for anticancer drugs and subjected to the absorption, distribution, metabolism, excretion and toxicity (ADMET) evaluation. | URI: | https://open.uns.ac.rs/handle/123456789/17705 | ISSN: | 09280987 | DOI: | 10.1016/j.ejps.2017.05.004 (BISIS)104603 (BISIS)104603 |
Appears in Collections: | FINS Publikacije/Publications TF Publikacije/Publications |
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