Hydroxychloroquine as Potent Inhibitor of COVID-19 Main Protease: Grid Based Docking Approach

被引:2
|
作者
Malik, Jitender Kumar [1 ]
Soni, Himesh [2 ]
Sharma, Sarvesh [2 ]
Sarankar, Satish [3 ]
机构
[1] Bharat Inst Pharm, Dept Pharmaceut Chem, Sonepat, India
[2] DHS Bhopal, Bhopal, India
[3] IES Inst Pharm, Bhopal, India
来源
关键词
COVID-19; Hydroxychloroquine; Molecular Docking & Prevention measures; CORONAVIRUS;
D O I
10.14744/ejmo.2020.91607
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: Coronavirus (COVID-19) is an enveloped RNA virus that occurs in various forms in humans and wildlife. A total of six disease-causing species have been identified in humans. Viral infections play a vital role in human diseases, and recent outbreaks have developed globally in the form of novel corona. The SS-RNA virus from the enveloped coronavirus family caused SARS (Severe Acute Respiratory Syndrome), a life-threatening viral infection. In many countries around the world, the spread of infection is rapid. As of March 26, 2020, there were 462.684 confirmed cases globally, and 20.834 deaths were recorded. The World Health Organization (WHO) described COVID-19 as a pandemic on March 11, 2020. There are numerous drug trials going on with some positive results. However, since no vaccine is available, the best way to combat the virus is to use preventive methods. Methods: In this study, an attempt was made to find the new COVID-19 main protease inhibitor with a molecular docking approach. A grid-based docking approach was chosen to find the binding using VLife MDS software. The 2D structure of the compounds was created and then converted into the 3D, and then, it was energetically minimized up to the RMS gradient of 0.01, using the Merck Molecular Force Field (MMFF). By using cavity determination option, the enzyme's cavities were determined. Cavity no.1 was selected for docking. The active site for docking was defined as all atoms within 5A degrees radius. Results: Hydroxychloroquine is a slow-acting antirheumatic drug. The value of hydroxychloroquine is analogous to that reported for other disease-modifying anti-rheumatic drugs. The docking score obtained was -4.308880 and the number of receptor atoms was 77, while the number of ligand atoms was 20, which shows that hydroxychloroquine binds effectively with Covid-19 protease. Conclusion: Hydroxychloroquine was taken as drug following Lipinski's rule of five, so it had a very good drug score and drug-likeness score as well. This study reveals that Hydroxychloroquine has good binding affinity with COVID-19 protease and thus can be used as prophylaxis and therapeutic treatment for corona patients.
引用
收藏
页码:219 / 226
页数:8
相关论文
共 50 条
  • [1] Molecular docking identification for the efficacy of some zinc complexes with chloroquine and hydroxychloroquine against main protease of COVID-19
    Hussein, R. K.
    Elkhair, H. M.
    JOURNAL OF MOLECULAR STRUCTURE, 2021, 1231
  • [2] Vitamin D is a New Promising Inhibitor to the Main Protease (Mpro) of COVID-19 by Molecular Docking
    Al-Mazaideh, Ghassab M.
    Shalayel, Mohammed H.
    Al-Swailmi, Farhan K.
    Aladaileh, Saleem H.
    JOURNAL OF PHARMACEUTICAL RESEARCH INTERNATIONAL, 2021, 33 (29B) : 186 - 191
  • [3] Virtual screening based on molecular docking of possible inhibitors of Covid-19 main protease
    Marinho, Emanuelle Machado
    de Andrade Neto, Joao Batista
    Silva, Jacilene
    da Silva, Cecilia Rocha
    Cavalcanti, Bruno Coelho
    Marinho, Emmanuel Silva
    Nobre Junior, Helio Vitoriano
    MICROBIAL PATHOGENESIS, 2020, 148
  • [4] Tetrandrine, an Effective Inhibitor of COVID-19 Main Protease (Mpro); Insights from Molecular Docking and Dynamics Simulations
    Begum, S. K. Arifa
    Begum, Shaheen
    Bandari, Pranay
    Swapna, B.
    Reddemma, Maadhu
    INTERNATIONAL JOURNAL OF PHARMACEUTICAL INVESTIGATION, 2023, 13 (04) : 845 - 851
  • [5] Hordatines as a Potential Inhibitor of COVID-19 Main Protease and RNA Polymerase: An In-Silico Approach
    Mohammed A. Dahab
    Mostafa M. Hegazy
    Hatem S. Abbass
    Natural Products and Bioprospecting, 2020, 10 : 453 - 462
  • [6] Hordatines as a Potential Inhibitor of COVID-19 Main Protease and RNA Polymerase: An In-Silico Approach
    Dahab, Mohammed A.
    Hegazy, Mostafa M.
    Abbass, Hatem S.
    NATURAL PRODUCTS AND BIOPROSPECTING, 2020, 10 (06) : 453 - 462
  • [7] In silico Approach on Ribavirin Inhibitors for COVID-19 Main Protease
    Dhumad, Adil Muala
    Majeed, Hatem Jameel
    Harismah, Kun
    Zandi, Hasan
    BIOINTERFACE RESEARCH IN APPLIED CHEMISTRY, 2021, 11 (06): : 13924 - 13933
  • [8] Catechin Derivatives as Inhibitor of COVID-19 Main Protease (Mpro): Molecular Docking Studies Unveil an Opportunity Against CORONA
    Arif, Muhammad Nouman
    COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING, 2022, 25 (01) : 197 - 203
  • [9] Main protease inhibitors and drug surface hotspots for the treatment of COVID-19: A drug repurposing and molecular docking approach
    Hasan, Mahmudul
    Parvez, Md Sorwer Alam
    Azim, Kazi Faizul
    Imran, Md Abdus Shukur
    Raihan, Topu
    Gulshan, Airin
    Muhit, Samuel
    Akhand, Rubaiat Nazneen
    Ahmed, Syed Sayeem Uddin
    Uddin, Md Bashir
    BIOMEDICINE & PHARMACOTHERAPY, 2021, 140
  • [10] ANTIFUNGAL ACTIVITY, MOLECULAR DOCKING ON COVID-19 MAIN PROTEASE AND PHARMACOKINETICS OFIMIDAZOLONE ANALOGUES
    Vishnu, T.
    Sandhya, K.
    ArunaKumari, K.
    Aparna, Y.
    HETEROCYCLIC LETTERS, 2023, 13 (01): : 93 - 104