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Design and identification of novel annomontine analogues against SARS-CoV-2: An approach.

作者信息

Waidha Kamran, Saxena Anjali, Kumar Prashant, Sharma Sunil, Ray Devalina, Saha Biswajit

机构信息

Amity Institute of Biotechnology, Amity University Uttar Pradesh, Noida, 125, 201301, India.

Chemical Engineering Department, National Tsing Hua University, Hsinchu 30013, Taiwan.

出版信息

Heliyon. 2021 Apr;7(4):e06657. doi: 10.1016/j.heliyon.2021.e06657. Epub 2021 Apr 2.

DOI:10.1016/j.heliyon.2021.e06657
PMID:33824915
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8017494/
Abstract

AIMS

COVID-19 has currently emerged as the major global pandemic affecting the lives of people across the globe. It broke out from Wuhan Province of China, first reported to WHO on 31 December 2019 as "Pneumonia of unknown cause". Over time more people were infected with this virus, and the only tactic to ensure safety was to take precautionary measures due to the lack of any effective treatment or vaccines. As a result of unavailability of desired efficacy for previously repurposed drugs, exploring novel scaffolds against the virus has become the need of the hour.

MAIN METHODS

In the present study, 23 new annomontine analogues were designed representing -Carboline based scaffolds. A hypothesis on its role as an effective ligand was laid for target-specific binding in SARS-CoV-2. These molecules were used for molecular docking analysis against the multiple possible drug targets using the Maestro Interface. To ensure the drug safety of these molecules ADME/Tox analysis was also performed.

KEY FINDINGS

The molecular docking analysis of the 23 novel molecules indicated the efficiency of these derivates against COVID-19. The efficiency of molecules was computed by the summation of the docking score against each target defined as Lig and compared against Hydroxycholoquine as a standard. Based on the docking score, the majority of the annomontine derivatives were found to have increased binding affinity with targets as compared to hydroxycholoquine.

SIGNIFICANCE

Due to the lack of efficiency, effectiveness, and failure of already repurposed drugs against the COVID-19, the exploration of the novel scaffold that can act as effective treatment is much needed. The current study hence emphasizes the potential of Annomontine based - - Carboline derivatives as a potential drug candidate against COVID-19.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/496c30c45e0a/gr14.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/717cad0e3a48/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/01bb715917ba/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/d8a7dcb24e80/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/112e7d90e156/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/a041c05d1a91/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/d75d4b16d5c0/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/cc405a14441d/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/b26a9927e2ff/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/edf1d9f0bacf/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/3a8d5e3205e8/gr10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/4fd50c3ae3cb/gr11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/881e7229a310/gr12.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/b2ec7585aa0e/gr13.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/496c30c45e0a/gr14.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/717cad0e3a48/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/01bb715917ba/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/d8a7dcb24e80/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/112e7d90e156/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/a041c05d1a91/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/d75d4b16d5c0/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/cc405a14441d/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/b26a9927e2ff/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/edf1d9f0bacf/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/3a8d5e3205e8/gr10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/4fd50c3ae3cb/gr11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/881e7229a310/gr12.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/b2ec7585aa0e/gr13.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3945/8063754/496c30c45e0a/gr14.jpg

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2
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3
Chloroquine and hydroxychloroquine as ACE2 blockers to inhibit viropexis of 2019-nCoV Spike pseudotyped virus.
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Biology (Basel). 2023 Mar 29;12(4):519. doi: 10.3390/biology12040519.
氯喹和羟氯喹作为 ACE2 阻滞剂抑制 2019-nCoV Spike 假型病毒的病毒入侵。
Phytomedicine. 2020 Dec;79:153333. doi: 10.1016/j.phymed.2020.153333. Epub 2020 Sep 2.
4
TMPRSS2 and furin are both essential for proteolytic activation of SARS-CoV-2 in human airway cells.TMPRSS2 和 furin 均是 SARS-CoV-2 在人呼吸道细胞中蛋白水解激活所必需的。
Life Sci Alliance. 2020 Jul 23;3(9). doi: 10.26508/lsa.202000786. Print 2020 Sep.
5
Crystal Structure of the SARS-CoV-2 Non-structural Protein 9, Nsp9.严重急性呼吸综合征冠状病毒2非结构蛋白9(Nsp9)的晶体结构
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