Please use this identifier to cite or link to this item: http://hdl.handle.net/11189/9318
DC FieldValueLanguage
dc.contributor.authorYalo, Masandeen_US
dc.contributor.authorMakhaba, Masixoleen_US
dc.contributor.authorHussein, Ahmed Aen_US
dc.contributor.authorSharma, Rajanen_US
dc.contributor.authorKoki, Mkhuselien_US
dc.contributor.authorNako, Ndikhoen_US
dc.contributor.authorMabusela, Wilfred T.en_US
dc.date.accessioned2023-08-25T08:25:28Z-
dc.date.available2023-08-25T08:25:28Z-
dc.date.issued2022-
dc.identifier.citationYalo, M., Makhaba, M., Hussein, A.A. et al. 2022. Characterization of four new compounds from Protea cynaroides leaves and their tyrosinase inhibitory potential. Plants, 11(13): 1-13. [https://doi.org/10.3390/ 10.3390/plants11131751]en_US
dc.identifier.issn2223-7747-
dc.identifier.urihttp://hdl.handle.net/11189/9318-
dc.description.abstractProtea cynaroides (king protea) is a flowering plant that belongs to the Proteaceae family. This multi-stemmed shrub is the national flower of South Africa and has important economic and medicinal values. Traditionally, the main therapeutic benefits of this plant species include the treatment of cancer, bladder, and kidney ailments. There are very limited reports on the isolation of phytochemicals and their biological evaluation from P. cynaroides. In this study, the leaves of P. cynaroides were air-dried at room temperature, powdered, and extracted with 80% methanol followed by solvent fractionation (hexane, dichloromethane, ethyl acetate, and butanol). The ethyl acetate and butanol extracts were chromatographed and afforded four new (1–4) and four known (5–8) compounds, whose structures were characterized accordingly as 3,4-bis(4-hydroxybenzoyl)- 1,5-anhydro-D-glucitol (1), 4-hydroxybenzoyl-1,5-anhydro-D-glucitol (2), 2-(hydroxymethyl)-4-oxo- 4H-pyran-3-yl-6-O-benzoate- -D-glucopyranoside (3), 3-hydroxy-7,8-dihydro- -ionone 3-O- -Dglucopyranoside (4), 4-hydroxybenzoic acid (5), 1,5-anhydro-D-glucitol (6), 3,4-dihydroxybenzoic acid (7), and 3-hydroxykojic acid (8). The structural elucidation of the isolated compounds was determined based on 1D and 2D NMR, FTIR, and HRMS spectroscopy, as well as compared with the available literature data. The tyrosinase inhibitory activities of the extracts and isolated compounds were also determined. According to the results, compounds 7 and 8 exhibited potent competitive tyrosinase inhibitory activity against L-tyrosine substrates with IC50 values of 0.8776 0.012 and 0.7215 0.090 g/mL compared to the control (kojic acid, IC50 = 0.8347 0.093), respectively. This study is the first chemical investigation of compounds 1–4 from a natural source and the first report of the biological evaluation of compounds 1–5 against the tyrosinase enzyme. The potent anti-tyrosinase activity exhibited by P. cynaroides constituents will support future exploration of the plant in the cosmetic field upon further biological and clinical investigations.en_US
dc.language.isoenen_US
dc.publisherMDPIen_US
dc.relation.ispartofPlantsen_US
dc.subjectProteaceaeen_US
dc.subjectprotea cynaroidesen_US
dc.subjectphytochemistryen_US
dc.subjecttyrosinaseen_US
dc.titleCharacterization of four new compounds from Protea cynaroides leaves and their tyrosinase inhibitory potentialen_US
dc.identifier.doihttps://doi.org/10.3390/ 10.3390/plants11131751-
dc.typeArticleen_US
Appears in Collections:Appsc - Journal Articles (DHET subsidised)
Files in This Item:
File Description SizeFormat 
Characterization_Four_New_Compounds_Protea_cynaroides.pdf941.29 kBAdobe PDFView/Open
Show simple item record

Page view(s)

113
Last Week
0
Last month
3
checked on Aug 13, 2026

Download(s)

94
checked on Aug 13, 2026

Google ScholarTM

Check

Altmetric


Items in Digital Knowledge are protected by copyright, with all rights reserved, unless otherwise indicated.