Identification of α-glucosidase inhibitory compounds from Curcuma mangga fractions
Curcuma mangga is a medicinal plant, and its rhizomes are often used to treat various conditions, such as fever, thorax pain, itching, stomachaches, skin diseases, gout, and asthma. Although C. mangga is commonly used, information on the relationship between its chemical constituents and the bioacti...
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Formato: | Artigo |
Idioma: | English |
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Taylor and Francis
2020
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Acesso em linha: | http://psasir.upm.edu.my/id/eprint/89260/1/MANGGA.pdf |
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author | Awin, Tahani M. Mediani, Ahmed Mohd Faudzi, Siti Munirah Maulidiani, M. Sze, Wei Leong Shaari, Khozirah Abas, Faridah |
author_facet | Awin, Tahani M. Mediani, Ahmed Mohd Faudzi, Siti Munirah Maulidiani, M. Sze, Wei Leong Shaari, Khozirah Abas, Faridah |
author_sort | Awin, Tahani M. |
collection | UPM |
description | Curcuma mangga is a medicinal plant, and its rhizomes are often used to treat various conditions, such as fever, thorax pain, itching, stomachaches, skin diseases, gout, and asthma. Although C. mangga is commonly used, information on the relationship between its chemical constituents and the bioactivities of the rhizomes is still limited. The extraction solvents used have a strong effect on the metabolite profile and the bioactivity of the extract. A nuclear magnetic resonance (NMR)-based metabolomics approach was used to differentiate the metabolite profiles of hexane, chloroform, ethyl acetate, and methanol fractions of C. mangga rhizomes and to correlate the metabolites with α-glucosidase inhibitory activity. Primary and secondary metabolites were identified, including curcuminoids, carbohydrates, terpenoids, and amino acids. The ultra-performance liquid chromatography–tandem mass spectrometry (UPLC–MS/MS) analysis of the most active fraction (ethyl acetate) revealed the identification of additional metabolites, such as zerumin A, epigallocatechin, p-hydroxycinnamic, and copallic acids. A partial least square (PLS) biplot demonstrated that the existence of curcumin, demethoxycurcumin, curcumanggoside, calcaratarin A, labda-8(17),12-diene-15,16-dial, zerumin B, and difurocumenonol in the ethyl acetate fraction could be responsible for the α-glucosidase inhibitory activity. |
first_indexed | 2024-03-06T10:47:30Z |
format | Article |
id | upm.eprints-89260 |
institution | Universiti Putra Malaysia |
language | English |
last_indexed | 2024-03-06T10:47:30Z |
publishDate | 2020 |
publisher | Taylor and Francis |
record_format | dspace |
spelling | upm.eprints-892602021-09-03T08:59:45Z http://psasir.upm.edu.my/id/eprint/89260/ Identification of α-glucosidase inhibitory compounds from Curcuma mangga fractions Awin, Tahani M. Mediani, Ahmed Mohd Faudzi, Siti Munirah Maulidiani, M. Sze, Wei Leong Shaari, Khozirah Abas, Faridah Curcuma mangga is a medicinal plant, and its rhizomes are often used to treat various conditions, such as fever, thorax pain, itching, stomachaches, skin diseases, gout, and asthma. Although C. mangga is commonly used, information on the relationship between its chemical constituents and the bioactivities of the rhizomes is still limited. The extraction solvents used have a strong effect on the metabolite profile and the bioactivity of the extract. A nuclear magnetic resonance (NMR)-based metabolomics approach was used to differentiate the metabolite profiles of hexane, chloroform, ethyl acetate, and methanol fractions of C. mangga rhizomes and to correlate the metabolites with α-glucosidase inhibitory activity. Primary and secondary metabolites were identified, including curcuminoids, carbohydrates, terpenoids, and amino acids. The ultra-performance liquid chromatography–tandem mass spectrometry (UPLC–MS/MS) analysis of the most active fraction (ethyl acetate) revealed the identification of additional metabolites, such as zerumin A, epigallocatechin, p-hydroxycinnamic, and copallic acids. A partial least square (PLS) biplot demonstrated that the existence of curcumin, demethoxycurcumin, curcumanggoside, calcaratarin A, labda-8(17),12-diene-15,16-dial, zerumin B, and difurocumenonol in the ethyl acetate fraction could be responsible for the α-glucosidase inhibitory activity. Taylor and Francis 2020 Article PeerReviewed text en http://psasir.upm.edu.my/id/eprint/89260/1/MANGGA.pdf Awin, Tahani M. and Mediani, Ahmed and Mohd Faudzi, Siti Munirah and Maulidiani, M. and Sze, Wei Leong and Shaari, Khozirah and Abas, Faridah (2020) Identification of α-glucosidase inhibitory compounds from Curcuma mangga fractions. International Journal of Food Properties, 23 (1). 154 - 166. ISSN 1094-2912; ESSN: 1532-2386 https://www.tandfonline.com/doi/full/10.1080/10942912.2020.1716792 10.1080/10942912.2020.1716792 |
spellingShingle | Awin, Tahani M. Mediani, Ahmed Mohd Faudzi, Siti Munirah Maulidiani, M. Sze, Wei Leong Shaari, Khozirah Abas, Faridah Identification of α-glucosidase inhibitory compounds from Curcuma mangga fractions |
title | Identification of α-glucosidase inhibitory compounds from Curcuma mangga fractions |
title_full | Identification of α-glucosidase inhibitory compounds from Curcuma mangga fractions |
title_fullStr | Identification of α-glucosidase inhibitory compounds from Curcuma mangga fractions |
title_full_unstemmed | Identification of α-glucosidase inhibitory compounds from Curcuma mangga fractions |
title_short | Identification of α-glucosidase inhibitory compounds from Curcuma mangga fractions |
title_sort | identification of α glucosidase inhibitory compounds from curcuma mangga fractions |
url | http://psasir.upm.edu.my/id/eprint/89260/1/MANGGA.pdf |
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