Modulation of P‐glycoprotein activity by acridones and coumarins from Citrus sinensis
Identifieur interne : 000156 ( France/Analysis ); précédent : 000155; suivant : 000157Modulation of P‐glycoprotein activity by acridones and coumarins from Citrus sinensis
Auteurs : C. Bayet [France] ; C. Fazio [France] ; N. Darbour [France] ; O. Berger [France] ; I. Raad [France] ; A. Chaboud [France] ; C. Dumontet [France] ; D. Guilet [France]Source :
- Phytotherapy Research [ 0951-418X ] ; 2007-04.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Plante médicinale.
English descriptors
- KwdEn :
- Acridine derivatives, Acridines (isolation & purification), Acridines (pharmacology), Cell Line, Tumor, Citrus sinensis, Citrus sinensis (chemistry), Coumarine derivatives, Coumarins (isolation & purification), Coumarins (pharmacology), Humans, Inhibitor, Lactone, Medicinal plant, Molecular Structure, P Glycoprotein, P-Glycoprotein (antagonists & inhibitors), Pharmacognosy, Plant Roots (chemistry), Plant origin, P‐glycoprotein inhibitors, acridones, coumarins.
- MESH :
- chemical , antagonists & inhibitors : P-Glycoprotein.
- chemical , isolation & purification : Acridines, Coumarins.
- chemical , pharmacology : Acridines, Coumarins.
- chemistry : Citrus sinensis, Plant Roots.
- Cell Line, Tumor, Humans, Molecular Structure.
Abstract
Bioguided fractionation of the roots of Citrus sinensis (Rutaceae) led to the isolation and identification of five coumarins, namely, clausarin, suberosin, poncitrin, xanthyletin and thamnosmonin, seven acridones, namely, acrimarine B, 2‐methoxycitpressine I, citpressine I, buntanine, acrimarine E, honyumine and acrimarine C, and one terpenoid, namely, limonin. Among these compounds, clausarin, 2‐methoxycitpressine I and acrimarine E inhibited P‐glycoprotein‐mediated drug efflux in K562/R7 human leukemic cells over‐expressing P‐glycoprotein. Copyright © 2007 John Wiley & Sons, Ltd.
Url:
DOI: 10.1002/ptr.2081
Affiliations:
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<term>Citrus sinensis</term>
<term>Citrus sinensis (chemistry)</term>
<term>Coumarine derivatives</term>
<term>Coumarins (isolation & purification)</term>
<term>Coumarins (pharmacology)</term>
<term>Humans</term>
<term>Inhibitor</term>
<term>Lactone</term>
<term>Medicinal plant</term>
<term>Molecular Structure</term>
<term>P Glycoprotein</term>
<term>P-Glycoprotein (antagonists & inhibitors)</term>
<term>Pharmacognosy</term>
<term>Plant Roots (chemistry)</term>
<term>Plant origin</term>
<term>P‐glycoprotein inhibitors</term>
<term>acridones</term>
<term>coumarins</term>
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<keywords scheme="MESH" type="chemical" qualifier="isolation & purification" xml:lang="en"><term>Acridines</term>
<term>Coumarins</term>
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<term>Coumarins</term>
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<term>Molecular Structure</term>
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<term>Lactone</term>
<term>Origine végétale</term>
<term>Pharmacognosie</term>
<term>Plante médicinale</term>
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<front><div type="abstract" xml:lang="en">Bioguided fractionation of the roots of Citrus sinensis (Rutaceae) led to the isolation and identification of five coumarins, namely, clausarin, suberosin, poncitrin, xanthyletin and thamnosmonin, seven acridones, namely, acrimarine B, 2‐methoxycitpressine I, citpressine I, buntanine, acrimarine E, honyumine and acrimarine C, and one terpenoid, namely, limonin. Among these compounds, clausarin, 2‐methoxycitpressine I and acrimarine E inhibited P‐glycoprotein‐mediated drug efflux in K562/R7 human leukemic cells over‐expressing P‐glycoprotein. Copyright © 2007 John Wiley & Sons, Ltd.</div>
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