Author(s): Yogesh Vaishnav, Laxmi Banjare, Shekhar Verma, Govind Sharma, Deepak Biswas, Arpan Tripathi, Afzal B. Shaik, Richie R. Bhandare, Arvinder Kaur, Kavya Manjunath

Email(s): yogesh446688@gmail.com

DOI: 10.52711/0974-360X.2022.00922   

Address: Yogesh Vaishnav1*, Laxmi Banjare2, Shekhar Verma3, Govind Sharma1, Deepak Biswas1, Arpan Tripathi1, Afzal B. Shaik4, Richie R. Bhandare5,6, Arvinder Kaur7, Kavya Manjunath8
1Faculty of Pharmaceutical Sciences, Shri Shankaracharya Technical Campus, Junwani, Bhilai, 490020.
2School of Pharmaceutical Sciences, Guru Ghasidas Central University, Bilaspur – 495009 (C.G.) India.
3University College of Pharmacy, Pt Deendayal Upadhyay Memorial Health Sciences and Ayush University, Raipur, Chhattisgarh 493661.
4St. Mary’s College of Pharmacy, St. Mary’s Group of Institutions Guntur, Affiliated to Jawaharlal Nehru Technological University Kakinada, Chebrolu, Guntur, Andhra Pradesh, 522212.
5Department of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, Ajman University, Ajman, United Arab Emirates.
6Centre of Medical and Bio-allied Health Sciences Research, Ajman Uniersity, Ajman, United Arab Emirates.
7Department of Pharmaceutics, KLE College of Pharmacy, Bengaluru

Published In:   Volume - 15,      Issue - 12,     Year - 2022


ABSTRACT:
World is facing a new pandemic called covid-19SARS-CoV-2) since a year ago. Unfortunately there is no treatment for Covid 19 nowadays as well as no potential therapies has been developed to overcome from coronavirus pandemic. Some potential drug molecules with combination have ability to respond for covid19 virus. From the research it was found that the reduction of viral load can be treated with hydroxychloroquine and azithromycin combination. We evaluate the mode of interactions of hydroxychloroquine and azithromycin with the dynamic site of SARS-CoV-2 coronavirus main protease. Molecular Structure-based computational approach viz. molecular docking simulations were performed to scale up their affinity and binding fitness of the docked complex of novel SARS-CoV-2 coronavirus protease and hydroxychloroquine and azithromycin. The natural inhibitor N3 of novel SARS-CoV-2 coronavirus protease were exhibited highest affinity in terms of MolDock score (-167.203Kcal/mol), and hydroxychloroquine was found with lowest target affinity (-55.917 Kcal/mol).The amino acid residue cysteine 145 and histidine 41 is bound covalently and formed hydrogen bond interaction with SARS-CoV-2 inhibitor known as inhibitor N3 as such, hydroxychloroquine and azithromycin also formed hydrogen bond interaction. The binding patterns of the inhibitor N3 of SARS-CoV-2 coronavirus main protease could be used as a guideline for medicinal chemist to explore their SARS-CoV-2 inhibitory potential.


Cite this article:
Yogesh Vaishnav, Laxmi Banjare, Shekhar Verma, Govind Sharma, Deepak Biswas, Arpan Tripathi, Afzal B. Shaik, Richie R. Bhandare, Arvinder Kaur, Kavya Manjunath. Computational Method on Hydroxychloroquine and Azithromycin for SARS-CoV-2: Binding Affinity Studies. Research Journal of Pharmacy and Technology2022; 15(12):5467-2. doi: 10.52711/0974-360X.2022.00922

Cite(Electronic):
Yogesh Vaishnav, Laxmi Banjare, Shekhar Verma, Govind Sharma, Deepak Biswas, Arpan Tripathi, Afzal B. Shaik, Richie R. Bhandare, Arvinder Kaur, Kavya Manjunath. Computational Method on Hydroxychloroquine and Azithromycin for SARS-CoV-2: Binding Affinity Studies. Research Journal of Pharmacy and Technology2022; 15(12):5467-2. doi: 10.52711/0974-360X.2022.00922   Available on: https://rjptonline.org/AbstractView.aspx?PID=2022-15-12-16


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