ABSTRACT
Three new prenylated stilbenes, named as cajanusins A-C (1-3), and one new natural product cajanusin D (4), along with six known derivatives (5-10) were isolated from the leaves of Cajanus cajan. Their structures were fully elucidated by means of extensive spectroscopic methods and comparison with data in the reported literatures. The new compounds of 1 and 2 were evaluated for in vitro cytotoxic activities against a panel of human cancer cell lines.
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the chemical constituents in the ethyl acerate extract of Lysimachia fortunei.</p><p><b>METHOD</b>The compounds were isolated by silica gel chromatography, and their structures were elucidated by NMR data and references.</p><p><b>RESULT</b>Nine natural constituents were isolated, and their structures were identified as 9, 19-cyclolanost-24-en-3-one (1), 24-ethyl-5alpha-cholesta-7, 22(E)-dien-3-one (2), 1-pentatriacontanol (3), beta-stigmasterol (4), 24-ethyl-5alpha-cholesta-7, 22(E)-dien-3beta-ol (5), palmitic acid (6), isorhamnetin (7), kaempferol (8) and quercetin (9) respectively.</p><p><b>CONCLUSION</b>All compounds mentioned above were isolated from this plant for the first time, and compound 1, 2 and 5 were obtained from the genus for the first time.</p>
Subject(s)
Cholestadienes , Chemistry , Flavonols , Chemistry , Kaempferols , Chemistry , Palmitic Acid , Chemistry , Plants, Medicinal , Chemistry , Primulaceae , Chemistry , Quercetin , Triterpenes , ChemistryABSTRACT
<p><b>OBJECTIVE</b>To study lipid-regulating action of 2, 3, 5, 4'-tetrahydroxy stilbene-2-O-beta-D-glucopyranoside (TSG) from Polygonum multiflorum on experimental model hyperlipidemic rats.</p><p><b>METHOD</b>TSG 90 and 180 mg x kg(-10 x d(-1), atorvastatin mg kg(-1) x d(-1) and saline 2 mL x d(-1) were administered to hyperlipidemic rats. Groups of rats were determined and compared with those of saline group. The LDLR and HMGR mRNA expression were also detected.</p><p><b>RESULT</b>TSG significantly reduced serum TC and LDL-C level and atherosclerosis index, increased the expression of LDLR in the liver cells.</p><p><b>CONCLUSION</b>TSG, which shows effects and mechanism in part like atorcastatin, is a major constituent with blood-lipid regulating effect of P. multiflorum and can be explored as a potent medication for hyperlipidemia. Effects on LDL-C and AI, as well as on gene expression of TSG were first reported.</p>