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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Main Authors: Awin, Tahani M., Mediani, Ahmed, Mohd Faudzi, Siti Munirah, Maulidiani, M., Sze, Wei Leong, Shaari, Khozirah, Abas, Faridah
Formato: Artigo
Idioma:English
Publicado em: Taylor and Francis 2020
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.
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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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