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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
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.
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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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