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1.
Nat Prod Commun ; 6(9): 1321-2, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21941906

ABSTRACT

A new acylated neohesperoside derivative, 1-octyl-4'-isovaleroyl-neohesperoside (1), was isolated from Geranium purpureum Vill. (Geraniaceae) together with the known compounds quercetin-3-rutinoside and gallic acid. The identification of the isolated compounds was carried out by spectroscopic analysis including 1D- and 2D- NMR (1H, 13C, COSY, HSQC and HMBC) spectroscopy and ESI-TOF-MS.


Subject(s)
Disaccharides/chemistry , Geranium/chemistry , Molecular Structure , Spectrum Analysis
2.
Nat Prod Commun ; 5(6): 899-902, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20614819

ABSTRACT

An investigation was made of the effects on endogenous antioxidant enzyme activities and H2O2-induced lipid peroxidation inhibition in human red blood cells of the crude MeOH extract and its EtOAc, n-BuOH, and H2O sub-extracts obtained from aerial parts of Geranium psilostemon Ledeb., as well as compounds isolated from the most active EtOAc extract. Gallic acid (1), methyl gallate (2), pusilagin (3), 1,3,6-tri-O-galloyl-beta-glucopyranoside (4), 1,2,3,4,6-penta-O-galloyl-beta-glucopyranoside (5), kaempferol (6), quercetin (7), kaempferol 7-O-alpha-rhamnopyranoside (8), and quercetin 7-O-alpha-rhamnopyranoside (9) were isolated from the aerial parts of the title plant, and their structures identified from spectroscopic (UV, 1D- and 2D- NMR) and spectrometric (TOF-MS) data. All extracts and isolated compounds inhibited H2O2-induced lipid peroxidation and also enhanced the activity of superoxide dismutase (SOD) and catalase (CAT).


Subject(s)
Antioxidants/chemistry , Antioxidants/metabolism , Geranium/chemistry , Geranium/metabolism , Erythrocytes/drug effects , Erythrocytes/metabolism , Humans , Hydrogen Peroxide , Lipid Peroxidation , Plant Components, Aerial/chemistry
3.
Phytother Res ; 16(1): 88-90, 2002 Feb.
Article in English | MEDLINE | ID: mdl-11807975

ABSTRACT

In this study, it was shown that abietic acid, an abietane diterpenoid, inhibited soybean 5-lipoxygenase (linoleate: oxygen oxidoreductase, EC 1.13.11.12) and an IC(50) of 29.5 +/- 1.29 microM was determined. Since the lipoxygenase pathway leads to the biosynthesis of leukotrienes this result supports the view that abietic acid may be used in the treatment of allergic reactions.


Subject(s)
Abies , Abietanes , Diterpenes/pharmacology , Enzyme Inhibitors/pharmacology , Lipoxygenase/metabolism , Phenanthrenes/pharmacology , Plant Extracts/pharmacology , Diterpenes/chemistry , Diterpenes/isolation & purification , Dose-Response Relationship, Drug , Enzyme Inhibitors/chemistry , Linoleic Acid/pharmacology , Molecular Structure , Phenanthrenes/chemistry , Phenanthrenes/isolation & purification , Plant Extracts/chemistry , Plant Extracts/isolation & purification
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