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Characterization of Four New Compounds from Protea cynaroides Leaves and Their Tyrosinase Inhibitory Potential
Protea 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 can...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9269349/ https://www.ncbi.nlm.nih.gov/pubmed/35807702 http://dx.doi.org/10.3390/plants11131751 |
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author | Yalo, Masande Makhaba, Masixole Hussein, Ahmed A. Sharma, Rajan Koki, Mkhuseli Nako, Ndikho Mabusela, Wilfred T. |
author_facet | Yalo, Masande Makhaba, Masixole Hussein, Ahmed A. Sharma, Rajan Koki, Mkhuseli Nako, Ndikho Mabusela, Wilfred T. |
author_sort | Yalo, Masande |
collection | PubMed |
description | Protea 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-β-D-glucopyranoside (3), 3-hydroxy-7,8-dihydro-β-ionone 3-O-β-D-glucopyranoside (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 IC(50) values of 0.8776 ± 0.012 and 0.7215 ± 0.090 µg/mL compared to the control (kojic acid, IC(50) = 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. |
format | Online Article Text |
id | pubmed-9269349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-92693492022-07-09 Characterization of Four New Compounds from Protea cynaroides Leaves and Their Tyrosinase Inhibitory Potential Yalo, Masande Makhaba, Masixole Hussein, Ahmed A. Sharma, Rajan Koki, Mkhuseli Nako, Ndikho Mabusela, Wilfred T. Plants (Basel) Article Protea 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-β-D-glucopyranoside (3), 3-hydroxy-7,8-dihydro-β-ionone 3-O-β-D-glucopyranoside (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 IC(50) values of 0.8776 ± 0.012 and 0.7215 ± 0.090 µg/mL compared to the control (kojic acid, IC(50) = 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. MDPI 2022-06-30 /pmc/articles/PMC9269349/ /pubmed/35807702 http://dx.doi.org/10.3390/plants11131751 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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/). |
spellingShingle | Article Yalo, Masande Makhaba, Masixole Hussein, Ahmed A. Sharma, Rajan Koki, Mkhuseli Nako, Ndikho Mabusela, Wilfred T. Characterization of Four New Compounds from Protea cynaroides Leaves and Their Tyrosinase Inhibitory Potential |
title | Characterization of Four New Compounds from Protea cynaroides Leaves and Their Tyrosinase Inhibitory Potential |
title_full | Characterization of Four New Compounds from Protea cynaroides Leaves and Their Tyrosinase Inhibitory Potential |
title_fullStr | Characterization of Four New Compounds from Protea cynaroides Leaves and Their Tyrosinase Inhibitory Potential |
title_full_unstemmed | Characterization of Four New Compounds from Protea cynaroides Leaves and Their Tyrosinase Inhibitory Potential |
title_short | Characterization of Four New Compounds from Protea cynaroides Leaves and Their Tyrosinase Inhibitory Potential |
title_sort | characterization of four new compounds from protea cynaroides leaves and their tyrosinase inhibitory potential |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9269349/ https://www.ncbi.nlm.nih.gov/pubmed/35807702 http://dx.doi.org/10.3390/plants11131751 |
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