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Ifedayo Victor Ogungbe
Researcher at Jackson State University
Publications - 42
Citations - 935
Ifedayo Victor Ogungbe is an academic researcher from Jackson State University. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 15, co-authored 35 publications receiving 768 citations. Previous affiliations of Ifedayo Victor Ogungbe include University of Alabama in Huntsville & Scripps Research Institute.
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The Potential of Secondary Metabolites from Plants as Drugs or Leads Against Protozoan Neglected Diseases – Part I
Thomas J. Schmidt,Sami A. Khalid,Alvaro J. Romanha,T. Ma. Alves,Maique W. Biavatti,Reto Brun,FB Da Costa,S. L. De Castro,Vitor F. Ferreira,M. V. G. de Lacerda,João Henrique G. Lago,Leonor L. Leon,Norberto Peporine Lopes,R. C. das Neves Amorim,Michael Niehues,Ifedayo Victor Ogungbe,Adrian Martin Pohlit,Marcus Tullius Scotti,William N. Setzer,M. de N. C. Soeiro,M. Steindel,Andre G. Tempone +21 more
TL;DR: The current review attempts to give an overview on the potential of such plant-derived natural products as antiprotozoal leads and/or drugs in the fight against NTDs.
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Antileishmanial phytochemical phenolics: molecular docking to potential protein targets.
TL;DR: Two aurones, one chalcone, five coumarins, six flavonoids, one isoflavonoid, three lignans, and one stilbenoid can be considered to be promising drug leads worthy of further investigation based on in-silico analysis of antiparasitic polyphenolics in this study.
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In-silico Leishmania Target Selectivity of Antiparasitic Terpenoids
TL;DR: The selectivity of the different classes of antiparasitic compounds for the protein targets considered in this work can be explored in fragment- and/or structure-based drug design towards the development of leads for new antileishmanial drugs.
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The Potential of Secondary Metabolites from Plants as Drugs or Leads against Protozoan Neglected Diseases-Part III: In-Silico Molecular Docking Investigations.
TL;DR: This review presents molecular docking studies of potential phytochemicals that target key protein targets in Leishmania spp, Trypanosoma spp.
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In-silico screening for anti-Zika virus phytochemicals
TL;DR: 43 compounds that have drug-like properties have exhibited remarkable docking profiles to one or more of the ZIKV protein targets, suggesting promise for natural and inexpensive antiviral therapy for this emerging tropical disease.