Structure-based assortment of herbal analogues against spike protein to restrict COVID-19 entry through hACE2 receptor: An in-silico approach

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dc.contributor.author Santra, Sourav
dc.contributor.author Das, Sasti Gopal
dc.contributor.author Halder, Suman Kumar
dc.contributor.author Ghosh, Kuntal
dc.date.accessioned 2022-03-14T09:13:18Z
dc.date.available 2022-03-14T09:13:18Z
dc.date.issued 2021
dc.identifier.issn 1588-4082
dc.identifier.uri https://mcc-idr.l2c2academy.co.in/xmlui/handle/123456789/373
dc.description Journal Articles en_US
dc.description.abstract On-going global pandemic COVID-19 has spread all over the world and has led to more than 1.97 million deaths till date. Natural compounds may be useful to protecting health in this perilous condition. Mechanism of shuttle entry of SARS-COV-2 virus is by interaction with viral spike protein with human angiotensin-converting enzyme-2 (ACE-2) receptor. To explore potential natural therapeutics, 213 important phytochemicals of nine medicinal plants Aconitum heterophyllum, Cassia angustifolia, Cymbopogon fl exuosus, Cymbopogon martinii, Nux vomica, Phyllanthus urinaria, Swertia chirayita, Justicia adhatoda, Vetiveria zizanioides were selected for in-silico molecular docking against the spike protein of SARS-COV-2 and compared with recently prescribed drug chloroquine, ramdesivir, lopinavir and hydroxychloroquine. Results revealed that rhamnocitrin of P. urinaria, 1,5-dihydroxy-3,8-dimethoxyxanthone of S. chirayita and laevojunenol of V. zizanioides potentially binds with the receptor binding site of SARS-COV-2 spike glycoprotein and more robustly destabilized the RBD-ACE-2 binding over chloroquine, ramdesivir, lopinavir and hydroxychloroquine. It was also found that laevojunenol, rhamnocitrin, and 1,5-dihydroxy-3,8-dimethoxyxanthone qualifi ed the criteria for drug-likeness as per Lipinski rule. After attachment of the selected phytochemical with the spike protein the affi nity of the later towards ACE-2 was minimized and the eff ect of 1,5-dihydroxy-3,8- dimethoxyxanthone and laevojunenol was superior. Hence, rhamnocitrin of P. urinaria, 1,5-dihydroxy-3,8-dimethoxyxanthone of S. chirayita and laevojunenol of V. zizanioides, are potential therapeutic molecules for SARS-COV-2, which upon binding with spike protein changes the affi nity of the spike towards ACE-2 and therefore restrict the entry of the virus into a human cell. Subsequent clinical validation is needed to confi rm these phytochemicals as drugs to combat COVID-19. en_US
dc.language.iso en en_US
dc.publisher Acta Biologica Szegediensis en_US
dc.subject angiotensin-converting-enzyme-2 en_US
dc.subject COVID-19 en_US
dc.subject Medicinal plants en_US
dc.subject Molecular docking en_US
dc.subject Spike glycoprotein en_US
dc.title Structure-based assortment of herbal analogues against spike protein to restrict COVID-19 entry through hACE2 receptor: An in-silico approach en_US
dc.type Article en_US


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