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1.
Bioorg Med Chem Lett ; 20(8): 2412-6, 2010 Apr 15.
Article de Anglais | MEDLINE | ID: mdl-20346658

RÉSUMÉ

Three new homoisoflavonoids (1-3) were isolated from the roots of Ophiopogon japonicus (Liliaceae). The structures of new metabolites were determined on the basis of spectroscopic analyses including 2D NMR. The anti-inflammatory activities of new compounds (1-3) were investigated by their effects on the release of the inflammatory chemokine eotaxin, stimulated by IL-4 and the combination of IL-4 and TNF-alpha in BEAS-2B cells, which mimics the in vivo conditions in bronchial allergic asthma.


Sujet(s)
Anti-inflammatoires/isolement et purification , Isoflavones/isolement et purification , Ophiopogon/composition chimique , Racines de plante/composition chimique , Anti-inflammatoires/composition chimique , Anti-inflammatoires/pharmacologie , Lignée cellulaire , Humains , Interleukine-4/pharmacologie , Isoflavones/composition chimique , Isoflavones/pharmacologie , Analyse spectrale/méthodes , Facteur de nécrose tumorale alpha/pharmacologie
2.
J Nat Prod ; 73(2): 192-6, 2010 Feb 26.
Article de Anglais | MEDLINE | ID: mdl-20104880

RÉSUMÉ

Two new dammarane-type glycosides, 2alpha,3beta,12beta,20S-tetrahydroxydammar-24-ene-3-O-[beta-d-glucopyranosyl(1-->4)-beta-d-glucopyranosyl]-20-O-[beta-d-xylopyranosyl-(1-->6)-beta-d-glucopyranoside] (1) and 2alpha,3beta,12beta,20S-tetrahydroxydammar-24-ene-3-O-beta-d-glucopyranosyl-20-O-[beta-d-6-O-acetylglucopyranosyl-(1-->2)-beta-d-glucopyranoside] (2), were isolated from a MeOH extract of the leaves of Gynostemma pentaphyllum. Their structures were elucidated by 1D and 2D NMR spectroscopic interpretation as well as by chemical studies. The isolated compounds showed potential inhibitory effects on eotaxin expression in BEAS-2B bronchial epithelial cells.


Sujet(s)
Glucosides/isolement et purification , Glucosides/pharmacologie , Hétérosides/isolement et purification , Hétérosides/pharmacologie , Gynostemma/composition chimique , Plantes médicinales/composition chimique , Triterpènes/isolement et purification , Triterpènes/pharmacologie , Bronches/cytologie , Bronches/effets des médicaments et des substances chimiques , Cellules épithéliales/effets des médicaments et des substances chimiques , Glucosides/composition chimique , Hétérosides/composition chimique , Humains , Structure moléculaire , Résonance magnétique nucléaire biomoléculaire , Feuilles de plante/composition chimique , Stéréoisomérie , Triterpènes/composition chimique , Vietnam ,
3.
Chem Pharm Bull (Tokyo) ; 56(12): 1725-8, 2008 Dec.
Article de Anglais | MEDLINE | ID: mdl-19043247

RÉSUMÉ

Four new flavonoids, 3'-formyl-4',6',4-trihydroxy-2'-methoxy-5'-methylchalcone (1), 3'-formyl-6',4-dihydroxy-2'-methoxy-5'-methylchalcone 4'-O-beta-D-glucopyranoside (2), (2S)-8-formyl-6-methylnaringenin (3), and (2S)-8-formyl-6-methylnaringenin 7-O-beta-D-glucopyranoside (4) were isolated from the buds of Cleistocalyx operculatus (Myrtaceae). The structures of the new metabolites (1-4) were determined on the basic of spectroscopic analyses including 2 dimensional NMR. Compounds 1 and 3 exhibited 1,1-diphenyl-2-picrylhydrazyl radical scavenging activity with IC(50) values of 22.8 and 27.1 microM, respectively.


Sujet(s)
Antioxydants/pharmacologie , Flavonoïdes/pharmacologie , Myrtaceae/composition chimique , Antioxydants/isolement et purification , Dérivés du biphényle , Dichroïsme circulaire , Flavonoïdes/composition chimique , Flavonoïdes/isolement et purification , Fleurs/composition chimique , Hydrolyse , Spectroscopie par résonance magnétique , Complexes multienzymatiques/composition chimique , Picrates/composition chimique , Extraits de plantes/composition chimique , Spectrométrie de masse ESI , Spectrophotométrie IR , Spectrophotométrie UV , bêta-Glucosidase/composition chimique
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