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1.
J Asian Nat Prod Res ; 9(6-8): 531-5, 2007.
Artículo en Inglés | MEDLINE | ID: mdl-17885840

RESUMEN

Phytochemical analysis of the MeOH extract of the fruiting bodies of Stropharia aeruginosa resulted in the isolation of three lanostane triterpenoids, aeruginosols A, B and C. The structures of the new compounds were determined by spectroscopic analysis. The biological activities of aeruginosols A, B and C were examined by bioassay with lettuce seedling.


Asunto(s)
Basidiomycota/química , Triterpenos/aislamiento & purificación , Bioensayo , Estructura Molecular , Análisis Espectral , Triterpenos/química
2.
J Asian Nat Prod Res ; 7(5): 735-40, 2005 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-16176906

RESUMEN

Three new lanostane triterpenoids, aeruginosic acid derivatives, were isolated from the fruiting bodies of Stropharia aeruginosa and their structures were determined on the basis of spectral data.


Asunto(s)
Basidiomycota/química , Triterpenos/aislamiento & purificación , Estructura Molecular , Triterpenos/química
3.
Nat Prod Res ; 19(4): 363-6, 2005 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-15938143

RESUMEN

N-Phenethylhexadecanamide was isolated from the MeOH extract of the fruiting bodies of the mushroom Laetiporus sulphureus together with eburicoic acid. Their structures were elucidated by spectroscopic methods.


Asunto(s)
Ácidos Palmíticos/química , Polyporaceae/química , Lanosterol/análogos & derivados , Lanosterol/química , Estructura Molecular
4.
Biosci Biotechnol Biochem ; 69(2): 287-92, 2005 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-15725652

RESUMEN

Three cyclohexenone derivatives, (4S,5S,6S)-5,6-epoxy-4-hydroxy-3-methoxy-5-methyl-cyclohex-2-en-1-one (1), (4R,5R)-4,5-dihydroxy-3-methoxy-5-methyl-cyclohex-2-en-1-one (2), and (4R,5S,6R)-4,5,6-trihydroxy-3-methoxy-5-methyl-cyclohex-2-en-1-one (3), were isolated from unpolished rice fermented with an xylariaceous endophytic fungus (strain YUA-026). The structures of three compounds were established on the basis of spectroscopic analyses and chemical conversion. The minimum inhibitory concentrations of 1 and 3 were 100 microg/ml and 400 microg/ml against Staphylococcus aureus, 100 microg/ml and 200 microg/ml against Pseudomonas aeruginosa, and 200 microg/ml and >400 microg/ml against Candida albicans, respectively. In addition, 1 and 3 exhibited phytotoxic activity against lettuce.


Asunto(s)
Antiinfecciosos/aislamiento & purificación , Basidiomycota/química , Ciclohexanonas/aislamiento & purificación , Antiinfecciosos/farmacología , Candida albicans/efectos de los fármacos , Ciclohexanonas/farmacología , Germinación/efectos de los fármacos , Lactuca/efectos de los fármacos , Pruebas de Sensibilidad Microbiana , Modelos Moleculares , Estructura Molecular , Pseudomonas aeruginosa/efectos de los fármacos , Semillas/efectos de los fármacos , Staphylococcus aureus/efectos de los fármacos
5.
Phytochemistry ; 65(4): 491-6, 2004 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-14759547

RESUMEN

Two sesquiterpenoids, fascicularones A and B, have been isolated from the culture broth of a poisonous mushroom, Naematoloma fasciculare. Their structures were determined using spectroscopic methods.


Asunto(s)
Agaricales/química , Sesquiterpenos/química , Agaricales/crecimiento & desarrollo , Estructura Molecular , Micelio/química , Micelio/crecimiento & desarrollo , Resonancia Magnética Nuclear Biomolecular , Sesquiterpenos/aislamiento & purificación
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