Flavonoids from the genus Euphorbia : isolation, structure, pharmacological activities and structure–activity relationships

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dc.contributor.author Magozwi, Douglas Kemboi
dc.contributor.author Dinala, Mmabatho
dc.contributor.author Mokwana, Nthabiseng
dc.contributor.author Siwe-Noundou, Xavier
dc.contributor.author Krause, Rui W. M.
dc.contributor.author Sonopo, Molahlehi
dc.contributor.author McGaw, Lyndy Joy
dc.contributor.author Augustyn, Wilma A.
dc.contributor.author Tembu, Vuyelwa Jacqueline
dc.date.accessioned 2022-02-28T06:51:05Z
dc.date.available 2022-02-28T06:51:05Z
dc.date.issued 2021-05
dc.description.abstract Plants of the genus Euphorbia are widely distributed across temperate, tropical and subtropical regions of South America, Asia and Africa with established Ayurvedic, Chinese and Malay ethnomedical records. The present review reports the isolation, occurrence, phytochemistry, biological properties, therapeutic potential and structure–activity relationship of Euphorbia flavonoids for the period covering 2000–2020, while identifying potential areas for future studies aimed at development of new therapeutic agents from these plants. The findings suggest that the extracts and isolated flavonoids possess anticancer, antiproliferative, antimalarial, antibacterial, anti-venom, anti-inflammatory, anti-hepatitis and antioxidant properties and have different mechanisms of action against cancer cells. Of the investigated species, over 80 different types of flavonoids have been isolated to date. Most of the isolated flavonoids were flavonols and comprised simple O-substitution patterns, C-methylation and prenylation. Others had a glycoside, glycosidic linkages and a carbohydrate attached at either C-3 or C-7, and were designated as D-glucose, L-rhamnose or glucorhamnose. The structure–activity relationship studies showed that methylation of the hydroxyl groups on C-3 or C-7 reduces the activities while glycosylation loses the activity and that the parent skeletal structure is essential in retaining the activity. These constituents can therefore offer potential alternative scaffolds towards development of new Euphorbia-based therapeutic agents. en_ZA
dc.description.department Paraclinical Sciences en_ZA
dc.description.librarian pm2022 en_ZA
dc.description.sponsorship NRF-TWAS, South Africa, National Research Foundation Research and Tshwane University of Technology, Pretoria, South Africa. en_ZA
dc.description.uri http://www.mdpi.com/journal/pharmaceuticals en_ZA
dc.identifier.citation Magozwi, D.K.; Dinala, M.; Mokwana, N.; Siwe-Noundou, X.; Krause, R.W.M.; Sonopo, M.; McGaw, L.J.; Augustyn, W.A.; Tembu, V.J. Flavonoids from the Genus Euphorbia: Isolation, Structure, Pharmacological Activities and Structure–Activity Relationships. Pharmaceuticals 2021, 14, 428. https://doi.org/10.3390/ph14050428. en_ZA
dc.identifier.issn 1424-8247 (online)
dc.identifier.other 10.3390/ ph14050428
dc.identifier.uri http://hdl.handle.net/2263/84247
dc.language.iso en en_ZA
dc.publisher MDPI en_ZA
dc.rights © 2021 by the authors. Licensee: MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/). en_ZA
dc.subject Euphorbia en_ZA
dc.subject Flavonoids en_ZA
dc.subject Pharmacological activities en_ZA
dc.subject Structure–activity relationship en_ZA
dc.subject.other Veterinary science articles SDG-03 en_ZA
dc.subject.other SDG-03: Good health and well-being
dc.title Flavonoids from the genus Euphorbia : isolation, structure, pharmacological activities and structure–activity relationships en_ZA
dc.type Article en_ZA


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