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1.
Planta Med ; 82(5): 414-7, 2016 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-26824624

RESUMO

Oryzaeins A-D (1-4), four new isocoumarin derivatives, along with five known ones (5-9) were isolated from solid cultures of an endophytic fungus Aspergillus oryzae. Their structures were elucidated by detailed spectroscopic analysis and by comparison with reported data of related derivatives. Among them, compounds 1 and 2 represent the first examples of isocoumarins possessing an unusual 2-oxopropyl group and a rare 3-hydroxypropyl group. Compounds 1 and 2 displayed moderate anti-tobacco mosaic virus activities with inhibition rates of 28.4% and 30.6%, respectively, at the concentration of 20 µM. The new compounds showed moderate inhibitory activities against several human tumor cell lines with IC50 values in the range of 2.8-8.8 µM. Supporting information available online at http://www.thieme-connect.de/products.


Assuntos
Antineoplásicos/farmacologia , Antivirais/farmacologia , Aspergillus oryzae/química , Isocumarinas/farmacologia , Vírus do Mosaico do Tabaco/efeitos dos fármacos , Antibacterianos/farmacologia , Antineoplásicos/isolamento & purificação , Antivirais/isolamento & purificação , Linhagem Celular Tumoral , China , Ensaios de Seleção de Medicamentos Antitumorais , Humanos , Estrutura Molecular
2.
Fitoterapia ; 103: 260-4, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-25937499

RESUMO

Four new flavones, tobaflavones E-H (1-4), together with two known flavones (5 and 6), were isolated from the leaves of Dali Tiandeng tobacco (a variety of Yunnan local air cured tobacco). Their structures were elucidated by spectroscopic methods, including extensive 1D- and 2D NMR techniques. Compound 2 is the first naturally occurring flavone bearing a (4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)methyl moiety. These compounds were also evaluated for their anti-tobacco mosaic virus (anti-TMV) activity. The results revealed that compounds 1 and 2 exhibited high anti-TMV activity with inhibition rate of 35.3% and 39.6%, respectively. The rates are higher than those of positive control. The other compounds also showed potential anti-TMV activity with inhibition rates in the range of 18.7-28.4%, respectively.


Assuntos
Antivirais/farmacologia , Flavonas/farmacologia , Nicotiana/química , Vírus do Mosaico do Tabaco/efeitos dos fármacos , Antivirais/isolamento & purificação , China , Flavonas/isolamento & purificação , Estrutura Molecular , Folhas de Planta/química
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