<b>Antimicrobial diterpenoid alkaloids from <i>Erythrophleum suaveolens</i> (Guill. & perr.) Brenan</b>

An investigation of the stem bark of <i>Erythrophleum suaveolens</i> (Guill. & Perr.) Brenan yielded the known amide norcassaide (<b>1</b>) and a new diterpenoid alkaloid named norerythrosuaveolide (<b>2</b>) which was characterized as 7&beta;-hydroxy-7-de...

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Main Authors: F.N. Ngounou, R.N. Manfouo, L.A. Tapondjou, D. Lontsi, V. Kuete, V. Penlap, F.X. Etoa, M-A.L. Dubois, B.L. Sondengam
Format: Article
Language:English
Published: Chemical Society of Ethiopia 2005-12-01
Series:Bulletin of the Chemical Society of Ethiopia
Subjects:
Online Access:http://www.ajol.info/index.php/bcse/article/view/21127
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spelling doaj-b40b6eb07cb9457db3d627ad999f57922020-11-24T23:36:20ZengChemical Society of EthiopiaBulletin of the Chemical Society of Ethiopia1011-39241726-801X2005-12-01192221226<b>Antimicrobial diterpenoid alkaloids from <i>Erythrophleum suaveolens</i> (Guill. & perr.) Brenan</b>F.N. NgounouR.N. ManfouoL.A. TapondjouD. LontsiV. KueteV. PenlapF.X. EtoaM-A.L. DuboisB.L. SondengamAn investigation of the stem bark of <i>Erythrophleum suaveolens</i> (Guill. & Perr.) Brenan yielded the known amide norcassaide (<b>1</b>) and a new diterpenoid alkaloid named norerythrosuaveolide (<b>2</b>) which was characterized as 7&beta;-hydroxy-7-deoxo-6-oxonorcassaide. The structures were established on the basis of one and two-dimensional <sup>1</sup>H and <sup>13</sup>C NMR spectral data. The compounds showed potent antimicrobial activities against bacteria and yeasts. http://www.ajol.info/index.php/bcse/article/view/21127<i>Erythrophleum suaveolens</i> (Guill. & Perr.) BrenanNorcassaideDiterpenoid alkaloidNorerythrosuaveolideAntimicrobial activitiesBacteriaYeasts
collection DOAJ
language English
format Article
sources DOAJ
author F.N. Ngounou
R.N. Manfouo
L.A. Tapondjou
D. Lontsi
V. Kuete
V. Penlap
F.X. Etoa
M-A.L. Dubois
B.L. Sondengam
spellingShingle F.N. Ngounou
R.N. Manfouo
L.A. Tapondjou
D. Lontsi
V. Kuete
V. Penlap
F.X. Etoa
M-A.L. Dubois
B.L. Sondengam
<b>Antimicrobial diterpenoid alkaloids from <i>Erythrophleum suaveolens</i> (Guill. & perr.) Brenan</b>
Bulletin of the Chemical Society of Ethiopia
<i>Erythrophleum suaveolens</i> (Guill. & Perr.) Brenan
Norcassaide
Diterpenoid alkaloid
Norerythrosuaveolide
Antimicrobial activities
Bacteria
Yeasts
author_facet F.N. Ngounou
R.N. Manfouo
L.A. Tapondjou
D. Lontsi
V. Kuete
V. Penlap
F.X. Etoa
M-A.L. Dubois
B.L. Sondengam
author_sort F.N. Ngounou
title <b>Antimicrobial diterpenoid alkaloids from <i>Erythrophleum suaveolens</i> (Guill. & perr.) Brenan</b>
title_short <b>Antimicrobial diterpenoid alkaloids from <i>Erythrophleum suaveolens</i> (Guill. & perr.) Brenan</b>
title_full <b>Antimicrobial diterpenoid alkaloids from <i>Erythrophleum suaveolens</i> (Guill. & perr.) Brenan</b>
title_fullStr <b>Antimicrobial diterpenoid alkaloids from <i>Erythrophleum suaveolens</i> (Guill. & perr.) Brenan</b>
title_full_unstemmed <b>Antimicrobial diterpenoid alkaloids from <i>Erythrophleum suaveolens</i> (Guill. & perr.) Brenan</b>
title_sort <b>antimicrobial diterpenoid alkaloids from <i>erythrophleum suaveolens</i> (guill. & perr.) brenan</b>
publisher Chemical Society of Ethiopia
series Bulletin of the Chemical Society of Ethiopia
issn 1011-3924
1726-801X
publishDate 2005-12-01
description An investigation of the stem bark of <i>Erythrophleum suaveolens</i> (Guill. & Perr.) Brenan yielded the known amide norcassaide (<b>1</b>) and a new diterpenoid alkaloid named norerythrosuaveolide (<b>2</b>) which was characterized as 7&beta;-hydroxy-7-deoxo-6-oxonorcassaide. The structures were established on the basis of one and two-dimensional <sup>1</sup>H and <sup>13</sup>C NMR spectral data. The compounds showed potent antimicrobial activities against bacteria and yeasts.
topic <i>Erythrophleum suaveolens</i> (Guill. & Perr.) Brenan
Norcassaide
Diterpenoid alkaloid
Norerythrosuaveolide
Antimicrobial activities
Bacteria
Yeasts
url http://www.ajol.info/index.php/bcse/article/view/21127
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