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جامعة الشهيد حمه لخضر — الواديبوابة البحث العلمي
مقال

Combined molecular docking and dynamics simulations studies of natural compounds as potent inhibitors against SARS-CoV-2 main protease

Mebarka Ouassaf، Salah Belaıdı✉، Samir Chtita✉، Touhami Lanez، Faizan Abul Qais، Md Amiruddin Hashmi

الملخّص

Main protease (Mpro) of SARS-CoV-2 is a key CoV enzyme that plays a pivotal role in mediating viral replication and transcription, making it an attractive drug target for SARS-CoV-2 the new strain of coronavirus. In this study, we evaluated biologically active compounds present in medicinal plants as potential SARS-CoV-2 Mpro inhibitors, using a molecular docking study with Autodock Vina software. Top seven compounds Afzelin, Phloroglucinol, Myricetin-3-O- rutinosid Tricin 7-neohesperidoside, Silybin, Kaempferol and Silychristin among 50 molecules of natural Origin (Algerian Medicinal plants) were selected which had better and significantly low binding energy as compared to the reference molecule with binding affinities of −9.3, −9.3, −9, −8.9, −8.5, 8.3 and −8.3 kcal mol−1 respectively. Then, we analyzed the ADME properties of the best 7 ligands using the Web server SwissADME. Two of small molecules have been shown to be the ideal candidates for further drug development. Finally, the stability of the both compounds complexed with Mpro was validated through molecular dynamics (MD) simulation, they displayed stable trajectory (RMSD, RMSF) and molecular properties with consistent interaction profile in molecular dynamics simulations, moreover, Silybin could form more stable complex with Mpro than Silychristin.Communicated by Ramaswamy H. Sarma

التفاصيل

اللغة الأصليةEnglish
المجلّةJournal of Biomolecular Structure and Dynamics
المجلّد40
العدد21
الصفحات11264-11273
الناشرTaylor & Francis
ISSN0739-1102 · 1538-0254
DOI10.1080/07391102.2021.1957712
حالة النشرمنشور — 27 جويلية 2021

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