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1.
China Journal of Chinese Materia Medica ; (24): 1183-1187, 2013.
Article in Chinese | WPRIM | ID: wpr-350637

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the chemical compounds from the ethanol extract with inhibitory effects against aldose reductase from Thunbergia.</p><p><b>METHOD</b>Guided by anti-aldose reductase assay, compounds from the bioactive fraction (ethyl acetate extract) were separated and purified by various chromatographic methods including silica gel, Sephadex LH-20, and reversed-phase HPLC. Their structures were indentified based on analysis of the spectroscopic data including 1D and 2D NMR data.</p><p><b>RESULT</b>Eight compounds were obtained and identified as 8-hydroxy-8-methyl-9-methene-cyclopentane [7,11] -1,4, 6-trihydroxy-tetrahydronaphthalene-12-one, named as thunbergia A (1), 3,4-dihydro-4,5,8-trihydroxy-2-(3-methyl-2-butenyl) naphtha[2,3-b] oxiren-1(2H)-one (2), 8-(beta-gluco pyranosyloxy)-3,4-dihydro-2-(3-methyl-2-butenyl)naphtha [2,3-b] oxiren-1(2H)-one (3), galangin (4), quercetin (5), luteolin (6), 5,6,3',4'-tetrahydroxy -3,7-dimethoxy-flavone (7) and upeol (8).</p><p><b>CONCLUSION</b>Thunbergia A was a new derivative of tetrahydronaphthalene, and compounds 2 and 3 were separated from the genus Thunbergia for the first time.</p>


Subject(s)
Animals , Rats , Acanthaceae , Chemistry , Aldehyde Reductase , Nuclear Magnetic Resonance, Biomolecular , Plant Extracts , Chemistry , Pharmacology , Plant Roots , Chemistry
2.
China Journal of Chinese Materia Medica ; (24): 1485-1488, 2006.
Article in Chinese | WPRIM | ID: wpr-316020

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the induction and culture of adventitious root of Panax notoginseng.</p><p><b>METHOD</b>Three ways, induction from the explants of three-year-old P. notoginseng. The explants of regenerated shoots and calluses, were used to induce adventitious roots. The effects of 2, 4-dichlorophenoxyacetic acid, indole-3-butyric acid and naphthylacetic acid on adventitious root induction were investigated respectively. The effects of four modes of separating adventitious roots from the parent tissues on culture in vitro were compared.</p><p><b>RESULT</b>Adventitious roots were successfully induced by three methods, of which the young flower bud callus was the best material for the induction of adventitious root. Indole-3-butyric acid possessed the strongest potency for induction. The liquid culture system was established by continuous culture of adventitious roots together with their parent tissues before separated.</p><p><b>CONCLUSION</b>The acquisition and culture in vitro in liquid culture system of adventitious roots of P. notoginseng lay a foundation for the next investigation.</p>


Subject(s)
2,4-Dichlorophenoxyacetic Acid , Pharmacology , Indoles , Pharmacology , Naphthaleneacetic Acids , Pharmacology , Panax notoginseng , Plant Growth Regulators , Pharmacology , Plant Roots , Plants, Medicinal , Tissue Culture Techniques , Methods
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