[Home ] [Archive]   [ فارسی ]  
:: Main :: About :: Current Issue :: Archive :: Search :: Submit :: Contact ::
:: Volume 20, Issue 3 (autumn 2020) ::
J Ardabil Univ Med Sci 2020, 20(3): 372-396 Back to browse issues page
Design of Potential Anti-Leishmanial Pharmacophores via In Silico Drug Repurposing
Sana Ahdeno , Nima Razaghi-Asl , Behnam Mohammadi-ghalehbin
Zoonoses Research Center, Ardabil University of Medical Sciences, Ardabil, Iran
Abstract:   (428 Views)
 
Background & objectives: Drug-repurposing is the study on application of existing drugs for treatment or control of other diseases. Major advantage of the technique relies on a nominated drug molecule that is applied for pharmacodynamics optimization due to lack of serious pharmacokinetics challenges. According to the importance of the subject, a present contribution has been dedicated to the in-silico analysis of a few drug classes with the aim of achieving potential anti-leishmanial pharmacophores.   
Methods: 3D structure of protein targets within leishmania parasite were retrieved from Brookhaven Protein Data Bank (PDB) on the basis of literature reports to evaluate the related complexes with drugs via molecular docking. Qualitative and quantitative analysis of drug-target interaction patterns in docked complexes offered drugs with higher binding affinities toward targets and finally structural patterns or hypothetical anti-leishmanial pharmacophores were proposed with regard to the top-ranked pharmaceutical compounds.
Results: Highest free binding energy could be estimated for Nateglinide in binding to farnesyl diphosphate synthase (ΔGb -13.30 kcal/mol). Among steroids, Norgestrel synthase (ΔGb -9.48 kcal/mol) and Testosterone synthase (ΔGb -8.05 kcal/mol) exhibited higher enzyme binding affinities and Arg82 was a key residue in making hydrogen bonds. Within fused tricyclic structural patterns, mirtazapine exhibited highest binding affinity to deoxy uridine triphosphate (ΔGb -8.64 kcal/mol). In Carbamazepine, amide substituent of the central ring facilitated the formation of two effective hydrogen bonds with Gln21 and Asn25 in deoxy uridine triphosphate. 
Conclusion: On the basis of obtained results for steroids and fused tricyclic scaffolds, it will be possible to design molecules that can inhibit several pathogenic targets simultaneously.
Keywords: Drug-Repurposing, Anti-Leishmanial Drug, Adenylyl Phosphoribosyl Transferase, Molecular Docking
Full-Text [PDF 1962 kb]   (182 Downloads)    
Type of Study: article | Subject: فارماکولوژی
Received: 2020/12/12 | Accepted: 2021/03/10 | Published: 2021/05/10
Add your comments about this article
Your username or Email:

CAPTCHA



XML   Persian Abstract   Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Ahdeno S, Razaghi-Asl N, Mohammadi-ghalehbin B. Design of Potential Anti-Leishmanial Pharmacophores via In Silico Drug Repurposing. J Ardabil Univ Med Sci. 2020; 20 (3) :372-396
URL: http://jarums.arums.ac.ir/article-1-1961-en.html


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Volume 20, Issue 3 (autumn 2020) Back to browse issues page
مجله دانشگاه علوم پزشکی اردبیل Journal of Ardabil University of Medical Sciences
Persian site map - English site map - Created in 0.09 seconds with 30 queries by YEKTAWEB 4331