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 |