Bioactive γ-lactones from the fermented broth of Neosartorya sp
| Autor: | Guei-Jane Wang, Chu-Huang Chen, Yu-Ming Ju, Sien-Sing Yang, Ya-Jing Tsau, Kuo-Fang Cheng, Tzong-Huei Lee |
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| Rok vydání: | 2010 |
| Předmět: |
Chemical structure
Ethyl acetate Neosartorya Pharmaceutical Science Nitric Oxide Synthase Type II Pharmacognosy Biology Chemical Fractionation Nitric Oxide Analytical Chemistry chemistry.chemical_compound Lactones Mice Cell Line Tumor Drug Discovery Medicinal fungi Animals Enzyme Inhibitors Chromatography High Pressure Liquid Pharmacology chemistry.chemical_classification Chromatography Organic Chemistry Chemical modification Esters Complementary and alternative medicine chemistry Biochemistry Fermentation Molecular Medicine Lactone Signal Transduction |
| Zdroj: | Planta medica. 76(15) |
| ISSN: | 1439-0221 |
| Popis: | Two γ-lactone derivatives, namely neosartolactone ( 1) and its 7-methyl ester analogue ( 2), have been isolated from the ethyl acetate extract of the fermented broth of NEOSARTORYA sp. isolated in Taiwan. Structural elucidations of compounds 1 and 2 were achieved on the basis of spectroscopic analysis. Although they had been obtained via the chemical modification of avenaciolide isolated from ASPERGILLUS AVENACEUS several decades ago, this is the first report to describe them from a natural resource with detailed spectroscopic interpretations. The effects of 1 and 2 on the inhibition of NO production in lipopolysaccharide (LPS)-activated murine macrophages were further evaluated. Compounds 1 and 2 significantly inhibited NO production with the IC 50 values of 12.2 ± 1.5 and 11.4 ± 1.0 μM, respectively; but displayed cytotoxicity at considerably higher concentrations than 50 μM. |
| Databáze: | OpenAIRE |
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