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Chemical Composition, Antifungal, and Cytotoxicity Activities of Inga laurina (Sw.) Willd Leaves
The species Inga laurina is native to the Brazilian Cerrado. There are no studies about the chemical composition and biological activities of extracts of this endangered species. The ethanolic extract and its successive fractions are rich in phenolic compounds and presented good antifungal activitie...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6377950/ https://www.ncbi.nlm.nih.gov/pubmed/30853865 http://dx.doi.org/10.1155/2019/9423658 |
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author | Martins, Carla de Moura de Morais, Sérgio A. L. Martins, Mário M. Cunha, Luís C. S. da Silva, Cláudio V. Martins, Carlos H. G. Leandro, Luís F. de Oliveira, Alberto de Aquino, Francisco J. T. do Nascimento, Evandro A. Chang, Roberto |
author_facet | Martins, Carla de Moura de Morais, Sérgio A. L. Martins, Mário M. Cunha, Luís C. S. da Silva, Cláudio V. Martins, Carlos H. G. Leandro, Luís F. de Oliveira, Alberto de Aquino, Francisco J. T. do Nascimento, Evandro A. Chang, Roberto |
author_sort | Martins, Carla de Moura |
collection | PubMed |
description | The species Inga laurina is native to the Brazilian Cerrado. There are no studies about the chemical composition and biological activities of extracts of this endangered species. The ethanolic extract and its successive fractions are rich in phenolic compounds and presented good antifungal activities. HPLC/MS-MS/MS and H1/C13 analysis led to the identification of seventeen compounds, most of which are gallic acid derivatives, myricetin and quercetin glycosides. The ethyl acetate fraction (EAF) contained high levels of total phenolics, expressed in milligrams of gallic acid equivalents per gram of extract (475.3 ± 1.9 mg GAE g(extract)(−1)) and flavonoids expressed in milligrams of quercetin equivalents per gram of extract (359.3 ± 10.6 mg QE g(extract)(−1)). This fraction was active against fungi of the Candida genus. The EAF showed MIC value 11.7 μg mL(−1) against C. glabrata and a selectivity index of 1.6 against Vero cells. The flavonol glycoside myricetin-3-O-rhamnoside was isolated for the first time from the Inga laurina. These results make I. laurina a promising plant as a source of pharmaceutical and biological active antifungal compounds. |
format | Online Article Text |
id | pubmed-6377950 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-63779502019-03-10 Chemical Composition, Antifungal, and Cytotoxicity Activities of Inga laurina (Sw.) Willd Leaves Martins, Carla de Moura de Morais, Sérgio A. L. Martins, Mário M. Cunha, Luís C. S. da Silva, Cláudio V. Martins, Carlos H. G. Leandro, Luís F. de Oliveira, Alberto de Aquino, Francisco J. T. do Nascimento, Evandro A. Chang, Roberto ScientificWorldJournal Research Article The species Inga laurina is native to the Brazilian Cerrado. There are no studies about the chemical composition and biological activities of extracts of this endangered species. The ethanolic extract and its successive fractions are rich in phenolic compounds and presented good antifungal activities. HPLC/MS-MS/MS and H1/C13 analysis led to the identification of seventeen compounds, most of which are gallic acid derivatives, myricetin and quercetin glycosides. The ethyl acetate fraction (EAF) contained high levels of total phenolics, expressed in milligrams of gallic acid equivalents per gram of extract (475.3 ± 1.9 mg GAE g(extract)(−1)) and flavonoids expressed in milligrams of quercetin equivalents per gram of extract (359.3 ± 10.6 mg QE g(extract)(−1)). This fraction was active against fungi of the Candida genus. The EAF showed MIC value 11.7 μg mL(−1) against C. glabrata and a selectivity index of 1.6 against Vero cells. The flavonol glycoside myricetin-3-O-rhamnoside was isolated for the first time from the Inga laurina. These results make I. laurina a promising plant as a source of pharmaceutical and biological active antifungal compounds. Hindawi 2019-02-03 /pmc/articles/PMC6377950/ /pubmed/30853865 http://dx.doi.org/10.1155/2019/9423658 Text en Copyright © 2019 Carla de Moura Martins et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Martins, Carla de Moura de Morais, Sérgio A. L. Martins, Mário M. Cunha, Luís C. S. da Silva, Cláudio V. Martins, Carlos H. G. Leandro, Luís F. de Oliveira, Alberto de Aquino, Francisco J. T. do Nascimento, Evandro A. Chang, Roberto Chemical Composition, Antifungal, and Cytotoxicity Activities of Inga laurina (Sw.) Willd Leaves |
title | Chemical Composition, Antifungal, and Cytotoxicity Activities of Inga laurina (Sw.) Willd Leaves |
title_full | Chemical Composition, Antifungal, and Cytotoxicity Activities of Inga laurina (Sw.) Willd Leaves |
title_fullStr | Chemical Composition, Antifungal, and Cytotoxicity Activities of Inga laurina (Sw.) Willd Leaves |
title_full_unstemmed | Chemical Composition, Antifungal, and Cytotoxicity Activities of Inga laurina (Sw.) Willd Leaves |
title_short | Chemical Composition, Antifungal, and Cytotoxicity Activities of Inga laurina (Sw.) Willd Leaves |
title_sort | chemical composition, antifungal, and cytotoxicity activities of inga laurina (sw.) willd leaves |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6377950/ https://www.ncbi.nlm.nih.gov/pubmed/30853865 http://dx.doi.org/10.1155/2019/9423658 |
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