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    <title>DSpace Collection:</title>
    <link>https://hdl.handle.net/20.500.12177/99</link>
    <description />
    <pubDate>Sat, 18 Apr 2026 13:42:15 GMT</pubDate>
    <dc:date>2026-04-18T13:42:15Z</dc:date>
    <item>
      <title>Chemical Study of the Essential Oils of Mischogyne elliotiana (Engl. &amp; Diels) (Annonaceae) and Daniellia ogea (Harms) Rolfe (Fabaceae), Obtained by Hydrodistillation and Steam Distillation</title>
      <link>https://hdl.handle.net/20.500.12177/13152</link>
      <description>Title: Chemical Study of the Essential Oils of Mischogyne elliotiana (Engl. &amp; Diels) (Annonaceae) and Daniellia ogea (Harms) Rolfe (Fabaceae), Obtained by Hydrodistillation and Steam Distillation
Authors: KOUAME, Bosson Antoine; N'DRI, Koffi Alfred; KONAN, N'dri Séraphin; MAMYRBÉKOVA-BEKRO, Janat Akhanovna; BEKRO, Yves-Alain
Abstract: Extracted from Mischogyne elliotiana and Daniellia ogea by hydrodistillation (HD) and steam&#xD;
distillation (SD) have been determined. EO yields are (HD: 0.012% - SD: 0.11%) for Mischogyne&#xD;
elliotiana and (HD: 0.06% - SD: 0.05%) for Daniellia ogea. Essential oils have been analyzed by&#xD;
Gas Chromatography-Mass Spectrometry. Essential oils obtained by hydrodistillation revealed&#xD;
more compounds than those obtained by steam distillation: Mischogyne elliotiana (HD: 32&#xD;
compounds - SD: 24 compounds), Daniellia ogea (HD: 40 compounds - SD: 38 compounds). The&#xD;
essential oils of Mischogyne elliotiana consist mainly of sesquiterpenes. The hydrocarbon&#xD;
sesquiterpene content is: (HD: 87.18% - SD: 94.27%). Oxygenated sesquiterpenes: (HD: 9.98% -&#xD;
SD: 3.76%). Daniellia ogea EO is made up of oxygenated sesquiterpenes (HD: 34.14% - EV:&#xD;
32.64%), diterpenes (HD: 2.07% - SD: 0.51%) and other compounds (HD: 7.15% - SD: 11.47%).&#xD;
Hydrocarbon monoterpenes (0.15%) are present only in the oil obtained by hydrodistillation. The&#xD;
main compounds in Mischogyne elliotiana EO obtained by hydrodistillation are α-gurjunene&#xD;
(58.14%) and β-guaiene (8.26%), while those obtained by steam distillation are α-gurjunene&#xD;
(50.60%) and β-guaiene (8.30%). In Daniellia ogea essential oils, the main compounds obtained by&#xD;
hydrodistillation are caryophyllene oxide (19.91%), β-caryophyllene (17.83%) and β-farnesene&#xD;
(15.56%), while those obtained by steam distillation are also caryophyllene oxide (18.92%) and β-&#xD;
caryophyllene (15.87%). The study on Mischogyne elliotiana essential oil is described for the first&#xD;
time.</description>
      <pubDate>Wed, 04 Mar 2026 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://hdl.handle.net/20.500.12177/13152</guid>
      <dc:date>2026-03-04T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Monomeric and oligomeric flavanols are agonists of membrane androgen receptors</title>
      <link>https://hdl.handle.net/20.500.12177/12973</link>
      <description>Title: Monomeric and oligomeric flavanols are agonists of membrane androgen receptors
Authors: Nifli, Artemissia-Phoebe; Kouamé, Bosson Antoine; Papadopoulou, Natalia; Kogia, Christina; Kampa, Marilena; Castagnino, Chantal; Stournaras, Christos; Vercauteren, Joseph; Castanas, Elias
Abstract: The present work reports a new mode of action of the naturally occurring flavanols catechin and epicatechin and their dimers B2 and B5,&#xD;
in the breast cancer T47D cell line, namely, their interaction with membrane androgen receptors. We show that monomeric and dimeric&#xD;
flavanols are complete (B2) or partial displacers of radiolabeled testosterone bound on T47D membranes, with affinities ranging from 1.7&#xD;
(B5) to 82.2 nM (B2). In addition, they trigger the phosphorylation of the same signaling molecules (FAK, PI3K) as testosterone-BSA,&#xD;
minutes after binding to membrane receptors, leading to actin cytoskeleton polymerization and redistribution, with formation of filopodia and&#xD;
lamellipodia. The PI3K inhibitor wortmannin reverts the effect of polyphenols and testosterone-BSA, providing additional evidence about&#xD;
activation of a similar signaling cascade. Incubation of T47D cells for more than 2 h with polyphenols or testosterone-BSA induces&#xD;
apoptosis, which follows the same time-dependent pattern. We conclude that flavanols (monomers or dimers) are agonists of membrane&#xD;
androgen receptors and could be used as testosterone – protein conjugates for the management of tumors, in which, application of&#xD;
testosterone-BSA induces regression, providing additional data about the mechanism of their antiproliferative action.</description>
      <pubDate>Tue, 21 Jun 2005 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://hdl.handle.net/20.500.12177/12973</guid>
      <dc:date>2005-06-21T00:00:00Z</dc:date>
    </item>
    <item>
      <title>COMPOSITION CHIMIQUE PAR GC/SM DES HUILES ESSENTIELLES EXTRAITES DES FEUILLES DE MIKANIA CORDATA (BURM. F.) B. L. ROBINSON ET DE SYNEDRELLA NODIFLORA (L.) GAERTN.</title>
      <link>https://hdl.handle.net/20.500.12177/12972</link>
      <description>Title: COMPOSITION CHIMIQUE PAR GC/SM DES HUILES ESSENTIELLES EXTRAITES DES FEUILLES DE MIKANIA CORDATA (BURM. F.) B. L. ROBINSON ET DE SYNEDRELLA NODIFLORA (L.) GAERTN.
Authors: Konan, N'dri Séraphin; Kouamé, Bosson Antoine; Mamyrbékova-Békro, Janat Akhanovna; Konan, Koffi Marcel; Békro, Yves-Alain
Abstract: Dans le but de contribuer à la valorisation la biodiversité floristique de Côte d’Ivoire&#xD;
en vue d’identifier de nouvelles molécules potentiellement intéressantes tant sur le plan&#xD;
biologique que thérapeutique, nous avons étudié la composition chimique des huiles&#xD;
essentielles (HE) issues des parties aériennes de Mikania cordata et de Synedrella nodiflora&#xD;
au moyen de la chromatographie en phase gazeuse couplée avec la spectrométrie de masse&#xD;
(GC/SM). Plus de 98,46% des composés ont été identifiés dans l’HE de chaque organe.&#xD;
L’HE de Synedrella nodiflora est constituée principalement de sesquiterpènes&#xD;
(90,31%), monoterpènes (6,93%) et d’autres composés (1,86%). Les composés majoritaires&#xD;
sont le β-caryophyllène (19,52%), le germacrène D (17,63%), le caryophyllène oxyde&#xD;
(10,50%) et le β-élémène (9,80%).&#xD;
Quant à celle de Mikania cordata, elle est composée de 44,20% de sesquiterpènes&#xD;
hydrocarbonés, 42,20% de monoterpènes, 9,20% de sesquiterpènes et de 2,98% d’autres&#xD;
composés. Ses principaux composés sont l’α-pinène (19,56%), le β-pinène (12,42%), le&#xD;
germacrène D (9,10%) et le β-caryophyllène (8,45%).</description>
      <pubDate>Tue, 04 Oct 2011 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://hdl.handle.net/20.500.12177/12972</guid>
      <dc:date>2011-10-04T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Chemical characterisation of essential oils of leaves of two Solanaceae: Solanum rugosum and Solanum erianthum from Côte d’Ivoire</title>
      <link>https://hdl.handle.net/20.500.12177/12971</link>
      <description>Title: Chemical characterisation of essential oils of leaves of two Solanaceae: Solanum rugosum and Solanum erianthum from Côte d’Ivoire
Authors: Kouao, Toffe Alexis; Kouamé, Bosson Antoine; Ouattara, Zana Adaman; Mamyrbekova-Bekro, Janat Akhanovna; Bighelli, Ange; Tomi, Felix; Békro, Yves-Alain
Abstract: This study made it possible to characterise by GC (in combination&#xD;
with retention indices), GC-MS and 13C NMR, the chemical com-&#xD;
position of the essential oils from Solanum rugosum and Solanum&#xD;
erianthum, two Solanaceae of the Ivorian flora. The two essential&#xD;
oils were characterised by a very high proportion of sesquiter-&#xD;
penes. Specifically, the essential oil of S. rugosum was dominated&#xD;
by (E)-b-caryophyllene (33.7%), b-elemol (19.8%) and germacrene&#xD;
D (14.4%), while that of S. erianthum was mainly composed of&#xD;
a-humulene (38.6%), b-elemol (17.8%) and (E)-b-caryophyllene&#xD;
(16.7%). The chemical composition of Solanum rugosum is&#xD;
described here for the first time.</description>
      <pubDate>Thu, 03 Oct 2019 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://hdl.handle.net/20.500.12177/12971</guid>
      <dc:date>2019-10-03T00:00:00Z</dc:date>
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