Please use this identifier to cite or link to this item: https://cris.library.msu.ac.zw//handle/11408/5310
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dc.contributor.authorF. L. Mtemelien_US
dc.contributor.authorJ Ndlovuen_US
dc.contributor.authorG Mugumbateen_US
dc.contributor.authorT Makwikwien_US
dc.contributor.authorR Shokoen_US
dc.date.accessioned2022-12-16T11:31:26Z-
dc.date.available2022-12-16T11:31:26Z-
dc.date.issued2022-05-27-
dc.identifier.urihttps://cris.library.msu.ac.zw//handle/11408/5310-
dc.description.abstractSchistosomiasis is a neglected tropical disease affecting over 250 million people worldwide. The disease is the second most prevalent neglected tropical disease after malaria. Treatment of schistosomiasis relies on the administration of praziquantel (also known as biltricide). Reliance on a single drug poses a threat to the public health system as the parasite may become resistant as shown by some laboratory findings. The possibility of the resistance rising to clinically significant levels has motivated the scientific community to search for new drug nominees. For a long time, natural products have always been a foundation for the identification of drug leads in the pharmaceutical industry. This paper reviews the progress made in the discovery of natural anti-schistosomal agents in the field of drug discovery. We focus mainly on natural products that have been tested on the schistosome parasite and exhibited potency. We also highlight applications of advanced techniques in drug discovery, with a major focus on computer-aided drug discovery methods. Specifically, we discuss structure-based drug discovery and ligand-based drug design approaches, with an emphasis on virtual screening.en_US
dc.language.isoenen_US
dc.publisherTaylor and Francis Groupen_US
dc.subjectSchistosomiasisen_US
dc.subjectpraziquantelen_US
dc.subjectschistosomicidalen_US
dc.subjectvirtual screeningen_US
dc.subjectnatural productsen_US
dc.titleAdvances in schistosomiasis drug discovery based on natural products.en_US
dc.typeresearch articleen_US
dc.relation.publicationAll LIfeen_US
dc.identifier.doihttps://doi.org/10.1080/26895293.2022.2080281-
dc.contributor.affiliationDepartment of Biology. Chinoyi University of Technology.Chinoyi Zimbabwe.en_US
dc.contributor.affiliationDepartment of Biology. Chinoyi University of Technology.Chinoyi Zimbabwe.en_US
dc.contributor.affiliationDepartment of Chemical Technology. Midlands State University.en_US
dc.contributor.affiliationDepartment of Pharmaceutical Sciences. Tshwane University of Technology,Pretoria South Africa.en_US
dc.contributor.affiliationDepartment of Biology, School of Natural Science and Mathematics.Chinoyi University of Technology.en_US
dc.relation.issn2689-5307en_US
dc.description.volume15en_US
dc.description.issue1en_US
dc.description.startpage608en_US
dc.description.endpage622en_US
item.openairetyperesearch article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.grantfulltextopen-
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