Author(s):
Pavlo V. Zadorozhnii, Vadym V. Kiselev, Anastasia E. Titova, Aleksandr V. Kharchenko, Ihor O. Pokotylo, Oxana V. Okhtina
Email(s):
torfp@i.ua
DOI:
10.5958/0974-360X.2017.00198.6
Address:
Pavlo V. Zadorozhnii*, Vadym V. Kiselev, Anastasia E. Titova, Aleksandr V. Kharchenko,
Ihor O. Pokotylo, Oxana V. Okhtina
Department of Organic Substances and Pharmaceutical Preparations, Ukrainian State University of Chemical Technology, Gagarin Ave., 8, Dnipro 49005, Ukraine.
*Corresponding Author
Published In:
Volume - 10,
Issue - 4,
Year - 2017
ABSTRACT:
In this paper, we have carried out in silico modeling of inhibition of enzyme Enoyl-ACP reductase (InhA) Mycobacterium tuberculosis N-5-aryl-1, 3, 4-oxadiazolo-2, 2-dichloroacetamidines using the software package ArgusLab 4.0.1. Based on the results of molecular docking we have selected compounds leaders that form more stable complexes with the enzyme as compared to known inhibitors. The studied compounds are a promising class of compounds with potential anti-TB activity, and they can be recommended for further research to treat this disease. The structures of the investigated compounds have been checked for compliance with Lipinski criteria. The prediction of acute toxicity in rats has been carried out in oral and intravenous routes of administration using GUSAR program.
Cite this article:
Pavlo V. Zadorozhnii, Vadym V. Kiselev, Anastasia E. Titova, Aleksandr V. Kharchenko, Ihor O. Pokotylo, Oxana V. Okhtina. Molecular Docking Studies of N-5-Aryl-1, 3, 4-oxadiazolo-2, 2-dichloroacet-amidines as Inhibitors of Enoyl-ACP Reductase Mycobacterium tuberculosi. Research J. Pharm. and Tech. 2017; 10(4): 1091-1097. doi: 10.5958/0974-360X.2017.00198.6
Cite(Electronic):
Pavlo V. Zadorozhnii, Vadym V. Kiselev, Anastasia E. Titova, Aleksandr V. Kharchenko, Ihor O. Pokotylo, Oxana V. Okhtina. Molecular Docking Studies of N-5-Aryl-1, 3, 4-oxadiazolo-2, 2-dichloroacet-amidines as Inhibitors of Enoyl-ACP Reductase Mycobacterium tuberculosi. Research J. Pharm. and Tech. 2017; 10(4): 1091-1097. doi: 10.5958/0974-360X.2017.00198.6 Available on: https://rjptonline.org/AbstractView.aspx?PID=2017-10-4-25