New natural products from Siphoneugena densiflora Berg (Myrtaceae) and their chemotaxonomic significance

Siphoneugena Berg (Myrtaceae) is a small eugenioid genus segregated from Eugenia by Berg. The phytochemical survey of Siphoneugena densiflora was carried out in order to find secondary metabolites which may be considered as chemotaxonomic characters and help to distinguish between the two genera. Five novel hydrolysable tannins were isolated from the methanolic extract of root bark and were characterized as ellagic acid 4-O-alpha-L-2"-O- and its isomer 4-O-alpha-L-3"-O-acetylrhamnopyranoside, siphoneugenin, that supports a new aglycone with a dibenzo-1,4-dioxin structure, 3,4'-di-O-methylellagic acid 4-O-beta-D-6"-O- and 4-O-beta-D-3",6"-diacetylglucopyranoside, accompanied by ellagic acid 4-O-alpha-L-4"-O-acetylrhamnopyranoside, eschweilenol C, sitosterol, daucosterol, rhamnose, casuarinin, castalagin, ellagic, gallic and syringic acids. From methanolic extract of leaves, in addition to the well known compounds quercetin, quercitrin, guiajaverin, reynoutrin, chebuloside II, terminolic, madecassic and asiatic acids, lupeol, alpha- and beta-amyrin, a new pentacyclic triterpene was isolated and named as beta-D-glucopyranosyl-2alpha,3beta,6beta-trihydroxyolean-12-en-28-ate. Structures were established on the basis of spectroscopic and chemical evidence, along with the comparison of the data reported in the literature.

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Main Authors: Gallo,Margareth B. C., Silva,Fernando C. da, Vieira,Paulo C., Fernandes,João B., Silva,Maria Fátima das G. F. da
Format: Digital revista
Language:English
Published: Sociedade Brasileira de Química 2006
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532006000200010
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spelling oai:scielo:S0103-505320060002000102006-04-17New natural products from Siphoneugena densiflora Berg (Myrtaceae) and their chemotaxonomic significanceGallo,Margareth B. C.Silva,Fernando C. daVieira,Paulo C.Fernandes,João B.Silva,Maria Fátima das G. F. da Siphoneugena densiflora Myrtaceae chemotaxonomy hydrolysable tannin pentacyclic triterpene Siphoneugena Berg (Myrtaceae) is a small eugenioid genus segregated from Eugenia by Berg. The phytochemical survey of Siphoneugena densiflora was carried out in order to find secondary metabolites which may be considered as chemotaxonomic characters and help to distinguish between the two genera. Five novel hydrolysable tannins were isolated from the methanolic extract of root bark and were characterized as ellagic acid 4-O-alpha-L-2"-O- and its isomer 4-O-alpha-L-3"-O-acetylrhamnopyranoside, siphoneugenin, that supports a new aglycone with a dibenzo-1,4-dioxin structure, 3,4'-di-O-methylellagic acid 4-O-beta-D-6"-O- and 4-O-beta-D-3",6"-diacetylglucopyranoside, accompanied by ellagic acid 4-O-alpha-L-4"-O-acetylrhamnopyranoside, eschweilenol C, sitosterol, daucosterol, rhamnose, casuarinin, castalagin, ellagic, gallic and syringic acids. From methanolic extract of leaves, in addition to the well known compounds quercetin, quercitrin, guiajaverin, reynoutrin, chebuloside II, terminolic, madecassic and asiatic acids, lupeol, alpha- and beta-amyrin, a new pentacyclic triterpene was isolated and named as beta-D-glucopyranosyl-2alpha,3beta,6beta-trihydroxyolean-12-en-28-ate. Structures were established on the basis of spectroscopic and chemical evidence, along with the comparison of the data reported in the literature.info:eu-repo/semantics/openAccessSociedade Brasileira de QuímicaJournal of the Brazilian Chemical Society v.17 n.2 20062006-04-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532006000200010en10.1590/S0103-50532006000200010
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language English
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author Gallo,Margareth B. C.
Silva,Fernando C. da
Vieira,Paulo C.
Fernandes,João B.
Silva,Maria Fátima das G. F. da
spellingShingle Gallo,Margareth B. C.
Silva,Fernando C. da
Vieira,Paulo C.
Fernandes,João B.
Silva,Maria Fátima das G. F. da
New natural products from Siphoneugena densiflora Berg (Myrtaceae) and their chemotaxonomic significance
author_facet Gallo,Margareth B. C.
Silva,Fernando C. da
Vieira,Paulo C.
Fernandes,João B.
Silva,Maria Fátima das G. F. da
author_sort Gallo,Margareth B. C.
title New natural products from Siphoneugena densiflora Berg (Myrtaceae) and their chemotaxonomic significance
title_short New natural products from Siphoneugena densiflora Berg (Myrtaceae) and their chemotaxonomic significance
title_full New natural products from Siphoneugena densiflora Berg (Myrtaceae) and their chemotaxonomic significance
title_fullStr New natural products from Siphoneugena densiflora Berg (Myrtaceae) and their chemotaxonomic significance
title_full_unstemmed New natural products from Siphoneugena densiflora Berg (Myrtaceae) and their chemotaxonomic significance
title_sort new natural products from siphoneugena densiflora berg (myrtaceae) and their chemotaxonomic significance
description Siphoneugena Berg (Myrtaceae) is a small eugenioid genus segregated from Eugenia by Berg. The phytochemical survey of Siphoneugena densiflora was carried out in order to find secondary metabolites which may be considered as chemotaxonomic characters and help to distinguish between the two genera. Five novel hydrolysable tannins were isolated from the methanolic extract of root bark and were characterized as ellagic acid 4-O-alpha-L-2"-O- and its isomer 4-O-alpha-L-3"-O-acetylrhamnopyranoside, siphoneugenin, that supports a new aglycone with a dibenzo-1,4-dioxin structure, 3,4'-di-O-methylellagic acid 4-O-beta-D-6"-O- and 4-O-beta-D-3",6"-diacetylglucopyranoside, accompanied by ellagic acid 4-O-alpha-L-4"-O-acetylrhamnopyranoside, eschweilenol C, sitosterol, daucosterol, rhamnose, casuarinin, castalagin, ellagic, gallic and syringic acids. From methanolic extract of leaves, in addition to the well known compounds quercetin, quercitrin, guiajaverin, reynoutrin, chebuloside II, terminolic, madecassic and asiatic acids, lupeol, alpha- and beta-amyrin, a new pentacyclic triterpene was isolated and named as beta-D-glucopyranosyl-2alpha,3beta,6beta-trihydroxyolean-12-en-28-ate. Structures were established on the basis of spectroscopic and chemical evidence, along with the comparison of the data reported in the literature.
publisher Sociedade Brasileira de Química
publishDate 2006
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532006000200010
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