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Two New Phenolic Constituents from the Stems of Euphorbia griffithii

ABSTRACT: Phytochemical studies on MeOH extract of stems of Euphorbia griffithii led to the isolation of one new hydrolyzable tannin dimer, corilagiffithiin (1) and one new galloyl-glucoside (2), alongside six known ones (3–8). Their structures and absolute configurations were determined by in depth...

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Autores principales: Kaunda, Joseph Sakah, Zhang, Ying-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6872693/
https://www.ncbi.nlm.nih.gov/pubmed/31734865
http://dx.doi.org/10.1007/s13659-019-00223-2
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author Kaunda, Joseph Sakah
Zhang, Ying-Jun
author_facet Kaunda, Joseph Sakah
Zhang, Ying-Jun
author_sort Kaunda, Joseph Sakah
collection PubMed
description ABSTRACT: Phytochemical studies on MeOH extract of stems of Euphorbia griffithii led to the isolation of one new hydrolyzable tannin dimer, corilagiffithiin (1) and one new galloyl-glucoside (2), alongside six known ones (3–8). Their structures and absolute configurations were determined by in depth spectroscopic analyses and comparison of their 1D NMR and MS data with literature reported values. Configurations of sugar moieties were determined by acidic hydrolysis and subsequent GC analysis of their corresponding trimethylsilylated l-cysteine adduct. At a concentration of 50 μM, compounds 1–3 showed no anti-inflammatory activities. GRAPHIC ABSTRACT: [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s13659-019-00223-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-68726932019-12-06 Two New Phenolic Constituents from the Stems of Euphorbia griffithii Kaunda, Joseph Sakah Zhang, Ying-Jun Nat Prod Bioprospect Original Article ABSTRACT: Phytochemical studies on MeOH extract of stems of Euphorbia griffithii led to the isolation of one new hydrolyzable tannin dimer, corilagiffithiin (1) and one new galloyl-glucoside (2), alongside six known ones (3–8). Their structures and absolute configurations were determined by in depth spectroscopic analyses and comparison of their 1D NMR and MS data with literature reported values. Configurations of sugar moieties were determined by acidic hydrolysis and subsequent GC analysis of their corresponding trimethylsilylated l-cysteine adduct. At a concentration of 50 μM, compounds 1–3 showed no anti-inflammatory activities. GRAPHIC ABSTRACT: [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s13659-019-00223-2) contains supplementary material, which is available to authorized users. Springer Singapore 2019-11-16 /pmc/articles/PMC6872693/ /pubmed/31734865 http://dx.doi.org/10.1007/s13659-019-00223-2 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Kaunda, Joseph Sakah
Zhang, Ying-Jun
Two New Phenolic Constituents from the Stems of Euphorbia griffithii
title Two New Phenolic Constituents from the Stems of Euphorbia griffithii
title_full Two New Phenolic Constituents from the Stems of Euphorbia griffithii
title_fullStr Two New Phenolic Constituents from the Stems of Euphorbia griffithii
title_full_unstemmed Two New Phenolic Constituents from the Stems of Euphorbia griffithii
title_short Two New Phenolic Constituents from the Stems of Euphorbia griffithii
title_sort two new phenolic constituents from the stems of euphorbia griffithii
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6872693/
https://www.ncbi.nlm.nih.gov/pubmed/31734865
http://dx.doi.org/10.1007/s13659-019-00223-2
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