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1.
Chem Pharm Bull (Tokyo) ; 53(4): 387-92, 2005 Apr.
Article in English | MEDLINE | ID: mdl-15802837

ABSTRACT

The methanolic extract from the flowers of Angelica furcijuga KITAGAWA was found to inhibit nitric oxide production in lipopolysaccharide-activated mouse peritoneal macrophages. From the methanolic extract, two new glycosides, hyuganosides IV and V, were isolated together with 28 known constituents. The structures of the new constituents were determined on the basis of chemical and physicochemical evidence. Furthermore, the inhibitory effects of 11 coumarin constituents on nitric oxide production were examined. Among them, 3'-angeloyl-cis-khellactone (IC(50)=82 microM), (S)-(-)-oxypeucedanin (57 microM), imperatorin (60 microM), isoepoxypteryxin (53 microM), and isopteryxin (8.8 microM) showed inhibitory activity.


Subject(s)
Angelica/chemistry , Benzofurans/chemistry , Benzofurans/pharmacology , Nitric Oxide/antagonists & inhibitors , Nitric Oxide/biosynthesis , Animals , Carbohydrate Conformation , Chromatography, High Pressure Liquid , Flowers/chemistry , Hydrolysis , In Vitro Techniques , Lipopolysaccharides/pharmacology , Macrophages/drug effects , Macrophages/metabolism , Magnetic Resonance Spectroscopy , Mice , Plant Extracts/chemistry , Spectrophotometry, Infrared
2.
Chem Pharm Bull (Tokyo) ; 51(4): 440-3, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12673002

ABSTRACT

The methanolic extract and its fractions from the fresh flowers of Prunus mume SIEB. et ZUCC. were found to show scavenging effects on 1,1-diphenylpicryl-2-hydrazyl (DPPH) radical and superoxide. The fragrance constituents of P. mume were analyzed by GC-MS and a new polyacylated sucrose, prunose III, was isolated from the ethyl acetate-soluble fraction. The structure of prunose III was determined on the basis of chemical and physicochemical evidence as 4,3',4',6'-tetra-O-acetyl-6-O-p-coumaroylsucrose. In addition, the scavenging effects of the principal constituents on DPPH radical and superoxide were examined.


Subject(s)
Flowers , Free Radical Scavengers/chemistry , Free Radical Scavengers/isolation & purification , Prunus , Sucrose/analogs & derivatives , Sucrose/chemistry , Acetylation , Free Radical Scavengers/pharmacology , Plant Extracts/chemistry , Plant Extracts/isolation & purification , Plant Extracts/pharmacology , Plants, Medicinal , Sucrose/isolation & purification
3.
J Nat Prod ; 65(8): 1151-5, 2002 Aug.
Article in English | MEDLINE | ID: mdl-12193020

ABSTRACT

The methanolic extract from the fresh flowers of Prunus mume exhibited inhibitory effects against aldose reductase and platelet aggregation. From the methanolic extract, two new flavonol oligoglycosides, 2' '-O-acetylrutin and 2' '-O-acetyl-3'-O-methylrutin, and two new polyacylated sucroses, prunoses I and II, were isolated together with 11 known constituents. The structures of 2' '-O-acetylrutin, 2' '-O-acetyl-3'-O-methylrutin, and prunoses I and II were determined on the basis of chemical and physicochemical evidence as quercetin 3-O-alpha-L-rhamnopyranosyl(1-->6)-2' '-O-acetyl-beta-D-glucopyranoside, 3'-O-methylquercetin 3-O-alpha-L-rhamnopyranosyl(1-->6)-2' '-O-acetyl-beta-D-glucopyranoside, 1,4,3',4',6'-penta-O-acetyl-6-O-p-coumaroylsucrose, and 1,3',4',6'-tetra-O-acetyl-6-O-p-coumaroylsucrose, respectively. The flavonol glycosides and prunose I were found to inhibit aldose reductase, while prunoses I and II inhibited platelet aggregation induced by thrombin.


Subject(s)
Aldehyde Reductase/antagonists & inhibitors , Blood Platelets/drug effects , Disaccharides/isolation & purification , Enzyme Inhibitors/isolation & purification , Flavonoids/isolation & purification , Glycosides/isolation & purification , Plants, Medicinal/chemistry , Sucrose/analogs & derivatives , Sucrose/isolation & purification , Algorithms , Animals , Chromatography, High Pressure Liquid , Disaccharides/chemistry , Disaccharides/pharmacology , Enzyme Inhibitors/chemistry , Enzyme Inhibitors/pharmacology , Flavonoids/chemistry , Flavonoids/pharmacology , Glycosides/chemistry , Glycosides/pharmacology , Hydrolysis , Japan , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Rabbits , Stereoisomerism , Sucrose/chemistry , Sucrose/pharmacology
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