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Evaluating the ability of some natural phenolic acids to target the main protease and AAK1 in SARS COV-2.


ABSTRACT: Researchers are constantly searching for drugs to combat the coronavirus pandemic caused by SARS-CoV-2, which has lasted for over two years. Natural compounds such as phenolic acids are being tested against Mpro and AAK1, which are key players in the SARS-CoV-2 life cycle. This research work aims to study the ability of a panel of natural phenolic acids to inhibit the virus's multiplication directly through Mpro and indirectly by affecting the adaptor-associated protein kinase-1 (AAK1). Pharmacophore mapping, molecular docking, and dynamic studies were conducted over 50 ns and 100 ns on a panel of 39 natural phenolic acids. Rosmarinic acid (16) on the Mpro receptor (- 16.33 kcal/mol) and tannic acid (17) on the AAK1 receptor (- 17.15 kcal/mol) exhibited the best docking energy against both receptors. These favourable docking score values were found to be superior to those of the co-crystallized ligands. Preclinical and clinical research is required before using them simultaneously to halt the COVID-19 life cycle in a synergistic manner.

SUBMITTER: Ghamry HI 

PROVIDER: S-EPMC10162004 | biostudies-literature | 2023 May

REPOSITORIES: biostudies-literature

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Evaluating the ability of some natural phenolic acids to target the main protease and AAK1 in SARS COV-2.

Ghamry Heba I HI   Belal Amany A   El-Ashrey Mohamed Kandeel MK   Tawfik Haytham O HO   Alsantali Reem I RI   Obaidullah Ahmad J AJ   El-Mansi Ahmed A AA   Abdelrahman Doaa D  

Scientific reports 20230505 1


Researchers are constantly searching for drugs to combat the coronavirus pandemic caused by SARS-CoV-2, which has lasted for over two years. Natural compounds such as phenolic acids are being tested against Mpro and AAK1, which are key players in the SARS-CoV-2 life cycle. This research work aims to study the ability of a panel of natural phenolic acids to inhibit the virus's multiplication directly through Mpro and indirectly by affecting the adaptor-associated protein kinase-1 (AAK1). Pharmaco  ...[more]

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