<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 7β-hydroxy-7-de...
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Chemical Society of Ethiopia
2005-12-01
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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 7β-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 7β-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 |
work_keys_str_mv |
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