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1.
Phytochem Anal ; 17(1): 20-4, 2006.
Article in English | MEDLINE | ID: mdl-16454472

ABSTRACT

(2S, 3S)-Taxifolin 3-O-arabinoside, a new dihydroflavonol glycoside, together with the known substances, (2R 3R)-taxifolin 3-O-arabinoside, astragalin, isoquercitrin, and cosmosiin, were isolated from the leaves of Trachelospermum jasminoides var. pubescens. Structural elucidation was carried out by spectroscopic methods, and the absolute configurations of C-2 and C-3 in taxifolin 3-O-arabinosides were determined on the basis of circular dichroism. Unlike the dihydroflavonol glycosides, (2R 3R)-taxifolin 3-O-glucoside and (2R, 3R-taxifolin 3-O-arabinoside, the novel (2S, 3S)-taxifolin 3-O-arabinoside is not effective as a zoospore attractant of the plant pathogenic fungus Aphanomyces cochlioides.


Subject(s)
Apocynaceae/chemistry , Glycosides/chemistry , Chromatography, High Pressure Liquid , Circular Dichroism , Molecular Structure , Plant Leaves/chemistry , Spectrometry, Mass, Fast Atom Bombardment , Spectrophotometry, Ultraviolet
2.
Phytochem Anal ; 14(1): 48-53, 2003.
Article in English | MEDLINE | ID: mdl-12597255

ABSTRACT

The threo and erythro forms of guaiacylglycerol-7'-O-methyl 8'-vanillic acid ethers, threo and erythro guaiacylglycerol 8'-vanillin ethers, and threo guaiacylglycerol 8'-(4-hydroxymethyl-2-methoxyphenyl) ether have been isolated from fruits of Boreava orientalis. Structural determinations were made on the basis of UV, MS, 1H- and 13C-NMR spectral data, including two-dimensional shift correlation. The relative configurations were assigned on the basis of 1H-NMR chemical shifts.


Subject(s)
Brassicaceae/chemistry , Guaifenesin/analogs & derivatives , Guaifenesin/analysis , Guaifenesin/chemistry , Magnetic Resonance Spectroscopy , Molecular Structure
3.
Nat Prod Lett ; 16(6): 383-7, 2002 Dec.
Article in English | MEDLINE | ID: mdl-12462342

ABSTRACT

Taxifolin 3-O-glucoside isomers, [(2R, 3R)-, (2R, 3S)-, (2S, 3R)- and (2S, 3S)-] were isolated from leaves of Chamaecyparis obtuse (Cupressaceae). Their structures were elucidated on the basis of UV, MS, CD, 1H- and 13C-NMR spectral data, including 2D shift correlation. It was found that the compounds could be distinguished by the use of 1H- and 13C-NMR spectral data.


Subject(s)
Chamaecyparis/chemistry , Glucosides/chemistry , Glucosides/isolation & purification , Quercetin/analogs & derivatives , Quercetin/chemistry , Quercetin/isolation & purification , Chromatography, High Pressure Liquid , Circular Dichroism , Japan , Medicine, Traditional , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Stereoisomerism
4.
Tohoku J Exp Med ; 197(3): 169-81, 2002 Jul.
Article in English | MEDLINE | ID: mdl-12365558

ABSTRACT

Protein tyrosine phosphatases (PTPases) play an essential role in the regulation of steady-state phosphorylation of the insulin receptor and other proteins in the insulin signaling pathway. To determine the role of PTPases in adipose tissue in the development into an insulin-resistant state, we examined PTPase activities and protein levels of three major candidate PTPases in adipose tissues of 26-week-old male Otsuka Long-Evans Tokushima Fatty (OLETF) rats. Particulate PTPase activities in visceral and epididymal adipose tissues of OLETF rats were increased compared to those in Long-Evans Tokushima Otsuka (LETO) rats, non-insulin-resistant controls. Cytosolic PTPase activities in these tissues were conversely decreased in OLETF rats. In subcutaneous adipose tissues, those changes were not observed. Western blot analysis showed that the amounts of leukocyte antigen-related PTPase (LAR), PTPase 1B (PTP1B), and src homology 2-containing PTPase (SH-PTP2) were increased in particulate fractions of visceral and epididymal fat of OLETF rats. On the other hand, those in the cytosolic fractions were slightly decreased. Troglitazone was administered to OLETF rats to examine the effect of the drug on the changes in PTPase activity and distribution. Troglitazone treatment restored those alterations in PTPase activity in the particulate fraction and the amounts of LAR, PTP1B and SH-PTP2 in both fractions of visceral and epididymal adipose tissues of OLETF rats. Although it remains unknown whether such effects of troglitazone are mediated by peroxisome proliferator-activated receptor y, these data provide useful information for understanding the significance of PTPase in insulin-resistant rats and the molecular mechanism of troglitazone action.


Subject(s)
Adipose Tissue/drug effects , Chromans/pharmacology , Hypoglycemic Agents/pharmacology , Protein Tyrosine Phosphatases/metabolism , Thiazoles/pharmacology , Thiazolidinediones , Adipose Tissue/cytology , Adipose Tissue/enzymology , Animals , Cell Fractionation , Diabetes Mellitus , Disease Models, Animal , Insulin Resistance/physiology , Male , Obesity , Protein Tyrosine Phosphatase, Non-Receptor Type 1 , Rats , Rats, Inbred OLETF , Rats, Long-Evans , Troglitazone
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