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  1. Article ; Online: Molecular binding studies of anthocyanins with multiple antiviral activities against SARS-CoV-2.

    Akinnusi, Precious Ayorinde / Olubode, Samuel Olawale / Salaudeen, Wasiu Adeboye

    Bulletin of the National Research Centre

    2022  Volume 46, Issue 1, Page(s) 102

    Abstract: Background: The search for ideal drugs with absolute antiviral activity against SARS-CoV-2 is still in place, and attention has been recently drawn to natural products. Several molecular targets have been identified as points of therapeutic intervention. ...

    Abstract Background: The search for ideal drugs with absolute antiviral activity against SARS-CoV-2 is still in place, and attention has been recently drawn to natural products. Several molecular targets have been identified as points of therapeutic intervention. The targets used in this study include SARS-CoV-2 helicase, spike protein, RNA-dependent RNA polymerase, main protease, and human ACE-2. An integrative computer-aided approach, which includes molecular docking, pharmacophore modeling, and pharmacokinetic profiling, was employed to identify anthocyanins with robust multiple antiviral activities against these SARS-CoV-2 targets.
    Result: Four anthocyanins (Delphinidin 3-O-glucosyl-glucoside, Cyanidin 3-O-glucosyl-rutinoside, Cyanidin 3-(p-coumaroyl)-diglucoside-5-glucoside), and Nasunin) with robust multiple inhibitory interactions were identified from a library of 118 anthocyanins using computer-aided techniques. These compounds exhibited very good binding affinity to the protein targets and moderate pharmacokinetic profiles. However, Cyanidin 3-O-glucosyl-rutinoside is reported to be the most suitable drug candidate with multiple antiviral effects against SARS-CoV-2 due to its good binding affinity to all five protein targets engaged in the study.
    Conclusions: The anthocyanins reported in this study exhibit robust binding affinities and strong inhibitory molecular interactions with the target proteins and could be well exploited as potential drug candidates with potent multiple antiviral effects against COVID-19.
    Language English
    Publishing date 2022-04-13
    Publishing country Germany
    Document type Journal Article
    ISSN 2522-8307
    ISSN (online) 2522-8307
    DOI 10.1186/s42269-022-00786-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Optimal molecular binding data and pharmacokinetic profiles of novel potential triple-action inhibitors of chymase, spleen tyrosine kinase, and prostaglandin D2 receptor in the treatment of asthma.

    Akinnusi, Precious Ayorinde / Olubode, Samuel Olawale / Adebesin, Ayomide Oluwadarasimi / Alade, Adebowale Abiodun / Nwoke, Victor Chinedu / Shodehinde, Sidiqat Adamson

    Journal, genetic engineering & biotechnology

    2023  Volume 21, Issue 1, Page(s) 113

    Abstract: Background: Asthma is a chronic and complex pulmonary condition that affects the airways. A total of 250,000 asthma-related deaths are recorded annually and several proteins including chymase, spleen tyrosine kinase, and prostaglandin D2 receptor have ... ...

    Abstract Background: Asthma is a chronic and complex pulmonary condition that affects the airways. A total of 250,000 asthma-related deaths are recorded annually and several proteins including chymase, spleen tyrosine kinase, and prostaglandin D2 receptor have been implicated in the pathophysiology of asthma. Different anti-inflammatory drugs have been developed for the treatment of asthma, particularly corticosteroids, but the associated adverse reactions cannot be overlooked. It is therefore of interest to identify and develop small molecule inhibitors of the integral proteins associated with asthma that have very little or no side effects. Herein, a molecular modeling approach was employed to screen the bioactive compounds in Chromolaena odorata and identify compounds with high binding affinity to the protein targets.
    Results: Five compounds were identified after rigorous and precise molecular screening namely (-)-epicatechin, chlorogenic acid, ombuine, quercetagetin, and quercetin 3-O-rutinoside. These compounds generally showed impressive binding to all the targets understudy. However, chlorogenic acid, quercetagetin, and quercetin 3-O-rutinoside showed better prospects in terms of triple-action inhibition. Further pulmonary and oral pharmacokinetics showed positive results for all the reported compounds. The generated pharmacophore model showed hydrogen bond donor, hydrogen bond acceptor, and aromatic rings as basic structural features required for triple action inhibition.
    Conclusion: These findings suggest that these compounds could be explored as triple-action inhibitors of the protein targets. They are, therefore, recommended for further analysis.
    Language English
    Publishing date 2023-11-10
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 2637420-1
    ISSN 2090-5920 ; 1687-157X ; 2090-5920
    ISSN (online) 2090-5920
    ISSN 1687-157X ; 2090-5920
    DOI 10.1186/s43141-023-00577-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Molecular docking, MMGBSA, and ADMET studies of phytoconstituents of

    Ajiboye, Basiru Olaitan / Fatoki, Toluwase Hezekiah / Akinnusi, Precious Ayorinde / Ajuwon, Olawale Rasaq / Oyinloye, Babatunji Emmanuel / Jeje, Temitope Olawale / Owolabi, Olutunmise Victoria / Ogedengbe, Oluwatosin O / Genovese, Claudia

    Natural product research

    2024  , Page(s) 1–9

    Abstract: ... O. ... ...

    Abstract O. gratissimum
    Language English
    Publishing date 2024-04-22
    Publishing country England
    Document type Journal Article
    ZDB-ID 2185747-7
    ISSN 1478-6427 ; 1478-6419
    ISSN (online) 1478-6427
    ISSN 1478-6419
    DOI 10.1080/14786419.2024.2344193
    Database MEDical Literature Analysis and Retrieval System OnLINE

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