Bioactive secondary metabolites from six trees of the family fabaceae (leguminosae)

A total of nineteen compounds are isolated from the six trees covered in this study.Four new cassane diterpenes 6B-hydroxy-vouacapen-5a-01 (CB33), 6B-benzoyl-7B-hydroxy-vouacapen-5a-01 (CB26) and 6B-benzoyl-8,9,11, 14-didehydro-vouacapen-5a-01 (CB 'isomer') were obtained from the DCM extra...

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Main Author: Hofileña, Joy G.
Format: text
Language:English
Published: Animo Repository 2002
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Online Access:https://animorepository.dlsu.edu.ph/etd_doctoral/1210
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Institution: De La Salle University
Language: English
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spelling oai:animorepository.dlsu.edu.ph:etd_doctoral-22112021-05-31T06:05:18Z Bioactive secondary metabolites from six trees of the family fabaceae (leguminosae) Hofileña, Joy G. A total of nineteen compounds are isolated from the six trees covered in this study.Four new cassane diterpenes 6B-hydroxy-vouacapen-5a-01 (CB33), 6B-benzoyl-7B-hydroxy-vouacapen-5a-01 (CB26) and 6B-benzoyl-8,9,11, 14-didehydro-vouacapen-5a-01 (CB 'isomer') were obtained from the DCM extract of Caesalpinia pulcherrima. Their structures were elucidated by extensive ID and 2D NMR analysis. CB22, a probable new furanoditerpene monoacetate variation of CB33, could not be fully elucidated due to its minimal amount and the presence of impurities. Four known compounds were also isolated namely, benzyl 2,6-dimethoxybenzoate (CB8), phytol (CB23), sitosterol (CB25), and squalene (CB36).The ethyl acetate extract of Pithecolobium dulce afforded kaempferol 3-a-L-rhamnoside (KM) and a 2:1 mixture of 1,3-glyceryl diacetate (KM3a) and 1,2-glyceryl diacetate (KM3b). Their structures were elucidated by 1D and 2D NMR analysis. 2002-01-01T08:00:00Z text https://animorepository.dlsu.edu.ph/etd_doctoral/1210 Dissertations English Animo Repository Plant metabolites Trees Legumes Microbial sensitivity tests Chemistry, Analytic Chemistry
institution De La Salle University
building De La Salle University Library
continent Asia
country Philippines
Philippines
content_provider De La Salle University Library
collection DLSU Institutional Repository
language English
topic Plant metabolites
Trees
Legumes
Microbial sensitivity tests
Chemistry, Analytic
Chemistry
spellingShingle Plant metabolites
Trees
Legumes
Microbial sensitivity tests
Chemistry, Analytic
Chemistry
Hofileña, Joy G.
Bioactive secondary metabolites from six trees of the family fabaceae (leguminosae)
description A total of nineteen compounds are isolated from the six trees covered in this study.Four new cassane diterpenes 6B-hydroxy-vouacapen-5a-01 (CB33), 6B-benzoyl-7B-hydroxy-vouacapen-5a-01 (CB26) and 6B-benzoyl-8,9,11, 14-didehydro-vouacapen-5a-01 (CB 'isomer') were obtained from the DCM extract of Caesalpinia pulcherrima. Their structures were elucidated by extensive ID and 2D NMR analysis. CB22, a probable new furanoditerpene monoacetate variation of CB33, could not be fully elucidated due to its minimal amount and the presence of impurities. Four known compounds were also isolated namely, benzyl 2,6-dimethoxybenzoate (CB8), phytol (CB23), sitosterol (CB25), and squalene (CB36).The ethyl acetate extract of Pithecolobium dulce afforded kaempferol 3-a-L-rhamnoside (KM) and a 2:1 mixture of 1,3-glyceryl diacetate (KM3a) and 1,2-glyceryl diacetate (KM3b). Their structures were elucidated by 1D and 2D NMR analysis.
format text
author Hofileña, Joy G.
author_facet Hofileña, Joy G.
author_sort Hofileña, Joy G.
title Bioactive secondary metabolites from six trees of the family fabaceae (leguminosae)
title_short Bioactive secondary metabolites from six trees of the family fabaceae (leguminosae)
title_full Bioactive secondary metabolites from six trees of the family fabaceae (leguminosae)
title_fullStr Bioactive secondary metabolites from six trees of the family fabaceae (leguminosae)
title_full_unstemmed Bioactive secondary metabolites from six trees of the family fabaceae (leguminosae)
title_sort bioactive secondary metabolites from six trees of the family fabaceae (leguminosae)
publisher Animo Repository
publishDate 2002
url https://animorepository.dlsu.edu.ph/etd_doctoral/1210
_version_ 1712576390207897600