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Targeting allosteric pockets of SARS-CoV-2 main protease Mpro.
Bhat, Zahoor Ahmad; Chitara, Dheeraj; Iqbal, Jawed; Sanjeev, B S; Madhumalar, Arumugam.
  • Bhat ZA; Multidisciplinary Centre for Advanced Research and Studies, Jamia Millia Islamia, New Delhi, India.
  • Chitara D; Department of Applied Sciences, Indian Institute of Information Technology, Allahabad, Allahabad, Uttar Pradesh, India.
  • Iqbal J; Multidisciplinary Centre for Advanced Research and Studies, Jamia Millia Islamia, New Delhi, India.
  • Sanjeev BS; Department of Applied Sciences, Indian Institute of Information Technology, Allahabad, Allahabad, Uttar Pradesh, India.
  • Madhumalar A; Multidisciplinary Centre for Advanced Research and Studies, Jamia Millia Islamia, New Delhi, India.
J Biomol Struct Dyn ; 40(14): 6603-6618, 2022 09.
Article in English | MEDLINE | ID: covidwho-1246561
ABSTRACT
Repurposing of antivirals is an attractive therapeutic option for the treatment of COVID-19. Main protease (Mpro), also called 3 C-like protease (3CLpro) is a key protease of SARS-CoV-2 involved in viral replication, and is a promising drug target for antivirals. A major challenge to test the efficacy of antivirals is the conformational plasticity of Mpro and its future mutation prone flexibility. Suitable choice of drugs in catalytic and allosteric pockets appear to be essential for combination therapy. Current study, based on docking and extensive set of MD simulations, finds the combination of Elbasvir, Glecaprevir and Ritonavir to be a viable candidate for further experimental drug testing/pharmacophore design for Mpro.Communicated by Ramaswamy H. Sarma.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Drug Treatment Limits: Humans Language: English Journal: J Biomol Struct Dyn Year: 2022 Document Type: Article Affiliation country: 07391102.2021.1891141

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Drug Treatment Limits: Humans Language: English Journal: J Biomol Struct Dyn Year: 2022 Document Type: Article Affiliation country: 07391102.2021.1891141