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1.
Planta Med ; 82(5): 414-7, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26824624

ABSTRACT

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.


Subject(s)
Antineoplastic Agents/pharmacology , Antiviral Agents/pharmacology , Aspergillus oryzae/chemistry , Isocoumarins/pharmacology , Tobacco Mosaic Virus/drug effects , Anti-Bacterial Agents/pharmacology , Antineoplastic Agents/isolation & purification , Antiviral Agents/isolation & purification , Cell Line, Tumor , China , Drug Screening Assays, Antitumor , Humans , Molecular Structure
2.
Fitoterapia ; 103: 260-4, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25937499

ABSTRACT

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.


Subject(s)
Antiviral Agents/pharmacology , Flavones/pharmacology , Nicotiana/chemistry , Tobacco Mosaic Virus/drug effects , Antiviral Agents/isolation & purification , China , Flavones/isolation & purification , Molecular Structure , Plant Leaves/chemistry
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