ABSTRACT
Nine secondary metabolites(S)-5-hydroxy-4-methylchroman-2-one(1), 4-methoxynaphthalene-1,5-diol(2), 8-methoxynaphthalene-1,7-diol(3), 1,8-dimethoxynaphthalene(4),(2R,4S)-2,3-dihydro-2-methyl-benzopyran-4,5-diol(5),(2R,4R)-3,4-dihydro-4-methoxy-2-methyl-2H-1-benzopyran-5-ol(6), 7-O-α-D-ribosyl-2,3-dihydro-5-hydroxy-2-methyl-chromen-4-one(7),(R)-3-methoxyl-1-(2,6-dihydroxyphenyl)-butan-1-one(8) and helicascolide A(9) were isolated from endophytic fungus Cladosporium sp. JJM22 by using column chromatographies of silica gel and ODS, and semi-preparative HPLC. Their structures were analyzed on the basis of spectroscopic and chemical data, especially NMR and MS. All isolated compounds were evaluated for their anti-inflammatory activities by examining the inhibitory activities on nitric oxide(NO) production induced by lipopolysaccharide in mouse macrophage RAW264.7 cells in vitro. Compounds 2-4 showed inhibitory activities.
Subject(s)
Animals , Mice , Benzopyrans , Cladosporium , Fungi , Molecular Structure , RhizophoraceaeABSTRACT
A new fatty acid methyl ester (1) was isolated from an EtOH extract of Fissistigma oldhamii. It structures was elucidated by a combination of HR-ESI-MS, 1D NMR, 2D NMR, UV, and IR spectroscopic data. The inhibitory effect of compound 1 on the proliferation of primary synovial cells was evaluated. As a result, it showed inhibitory effect on the proliferation of synoviocytes, with IC₅₀ value of 38.6 μmol·L⁻¹.
ABSTRACT
Objective: To study the chemical constituents from the leaves of Rhodomyrtus tomentosa and its antibacterial activities. Methods: The compounds were isolated and purified by various column chromatographies. Their structures were elucidated by means of spectral analyses (MS and NMR). The antibacterial activity of the compounds was tested by micro dilution method Results: A total of 21 compounds were isolated from the 95% ethanol extract in the leaves of R. tomentosa and identified as (2R,4'R,8'R)-α-tocopherol (1), (2R,4'R,8'R)-β-tocopherol (2), α-tocopherol-quinone (3), α-tocopherol A (4), (-)-a-tocospirone (5), rhodomyrtosone F (6), rhodomyrtosone C (7), watsonianone A (8), rhodomyrtone (9), verimol K (10), methyl cinnamate (11), naringenin (12), quercetin (13), myricetin (14), 3,7,3'-trimethoxy-5,4',5'-trihydroxy flavone (15), 5,7,3',5'- tetrahydroxyflavanone (16), blumeatin (17), dihydroquercetin-7,4'-dimethylether (18), dihydroquercetin-4'-dimethoxy (19), 2,4,7,8,9,10-hexahydroxy-3-methoxyanthracene-6-O-β-L-rhamnopyranoside (20), and 4,8,9,10-tetrahydroxy-2,3,7-trimethoxyanthracene-6-O-β-D-glucopyranoside (21). Conclusion: Compound 6 is a new natural product and compounds 2-5, 10-13, and 15-19 are isolated from the plants of Rhodomyrtus (DC.) Reich for the first time. Compounds 3 and 6-9 exhibit the antibacterial activities.
ABSTRACT
14 alkaloids were obtained from stems and leaves of Fissistigma oldhamii, by silica gel, ODS, Sephadex LH-20 column chromatographies, and semi-preparative HPLC. Using physicochemical and spectral methods, the isolated alkaloids were identified as norcepharadione B(1), asimilobine(2), lanuginosine(3), laurotanine(4), isocorydine(5), anolobine(6), xylopine(7), N-methylbuxifoline(8), aristolactam AIIIa(9), piperumbellactam A(10), goniopedaline(11), aristololactam BIII(12), liriodenine(13), and salutaridine(14), respectively. Compounds 3-5, 8, 10, 11 and 14 were isolated from the genus Fissistigma for the first time.