Abstract
Boesenbergia rotunda (L.) cyclohexenyl chalcone derivatives, 4-hydroxypanduratin A and panduratin A, showed good competitive inhibitory activities towards dengue 2 virus NS3 protease with the Ki values of 21 and 25 microM, respectively, whilst those of pinostrobin and cardamonin were observed to be non-competitive. NMR and GCMS spectroscopic data formed the basis of assignment of structures of the six compounds isolated.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Chalcone / analogs & derivatives*
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Chalcone / chemistry*
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Chalcone / pharmacology*
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Cyclohexanes / chemistry*
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Cyclohexanes / pharmacology*
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Flavonoids / chemistry*
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Flavonoids / pharmacology*
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Molecular Structure
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Plant Roots / chemistry
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Protease Inhibitors / chemistry*
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Protease Inhibitors / pharmacology*
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Serine Endopeptidases / metabolism*
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Zingiberaceae / chemistry*
Substances
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Cyclohexanes
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Flavonoids
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Protease Inhibitors
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cyclohexenyl chalcone
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Chalcone
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NS3 protease, dengue virus
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Serine Endopeptidases