Author(s): Olga Nesterova, Dmitrii Babaskin, Yuliya Tikhonova, Natalia Molodozhnikova, Sergey Kondrashev

Email(s): babaskindmit@rambler.ru

DOI: 10.52711/0974-360X.2021.00480   

Address: Olga Nesterova, Dmitrii Babaskin*, Yuliya Tikhonova, Natalia Molodozhnikova, Sergey Kondrashev
I. M. Sechenov First Moscow State Medical University, Moscow, Russian Federation.
*Corresponding Author

Published In:   Volume - 14,      Issue - 5,     Year - 2021


ABSTRACT:
The aim of the research is to study the effect of the synthesis of uracil derivatives on the HIV-1 activity. To achieve the goal, the following tasks were determined: to study the specificity of possible compounds for HIV-1 treatment; to synthesize uracil derivatives; to study the effect of the compounds on HIV-1 replication in vitro and select the most optimal concentrations, considering the cytotoxic effect; to determine the most effective anti-HIV-1 compounds for further research. Thus, nine new uracil analogues have been synthesized and proved to be inhibitors of HIV-1. Key structural modifications included replacement of the 6-chloro group of 1-benzyl-6-chloro-3-(3,5-dimethylbenzyl) uracil by other functional groups or N (1)-alkylation of 3-(3,5-dimethylbenzyl)-5-fluorouracil. These compounds showed only micromolar potency against HIV-1 in MT-4, though two of them; 6-azido-1-benzyl-3-(3,5-dimethylbenzyl) uracil and 6-amino-1-benzyl-3-(3,5-dimethylbenzyl) uracil were highly potent (half maximal effective concentration =0.081 and 0.069µM) and selective (selectivity index =679 and 658), respectively. Structure-activity relationships among the newly synthesized uracil analogues suggest the importance of the H-bond formed between 6-amino group of 6-amino-1-benzyl-3-(3,5-dimethylbenzyl) uracil and amide group of HIV-1 reverse transcriptase. Two 6-substituted 1-benzyl-3-(3,5-dimethylbenzyl) uracils, (6-azido-1-benzyl-3-(3,5-dimethylbenzyl) uracil and 6-amino-1-benzyl-3-(3,5-dimethylbenzyl) uracil) were discovered as novel anti-HIV agents. Compound’s activity against HIV-1 was determined based on inhibition of virus-induced cytopathogenicity in MT-4 cells. The compounds were tested for efficacy in infected cells and cytotoxicity. These compounds should be further pursued for their toxicity and pharmacokinetics in vivo as well as antiviral activity against non-nucleoside reverse transcriptase inhibitor-resistant strains. Thus, it will contribute to the development of a new generation of compounds effective against different viruses, considering their quickly mutation and increased resistance.


Cite this article:
Olga Nesterova, Dmitrii Babaskin, Yuliya Tikhonova, Natalia Molodozhnikova, Sergey Kondrashev. Effect of N'-Benzyl Substituted Uracil and the Analogues on HIV-1 Inhibition.Research Journal of Pharmacy and Technology. 2021; 14(5):2723-8. doi: 10.52711/0974-360X.2021.00480

Cite(Electronic):
Olga Nesterova, Dmitrii Babaskin, Yuliya Tikhonova, Natalia Molodozhnikova, Sergey Kondrashev. Effect of N'-Benzyl Substituted Uracil and the Analogues on HIV-1 Inhibition.Research Journal of Pharmacy and Technology. 2021; 14(5):2723-8. doi: 10.52711/0974-360X.2021.00480   Available on: https://rjptonline.org/AbstractView.aspx?PID=2021-14-5-64


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