Taipei Medical University

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Yang LM
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------>insert_date=20081119
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------>journal_name=Planta Med.
------>paper_name=Hydroxylation and glucosidation of ent-16beta-hydroxybeyeran-19-oic acid by Bacillus megaterium and Aspergillus niger
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------>fullAbstract=ent-16beta-Hydroxybeyeran-19-oic acid ( 1) has potential antihypertensive activity. To obtain novel and more-effective compounds, 1 was incubated with Bacillus megaterium ATCC 14 581 and Aspergillus niger CCRC 32 720. The structures of the metabolites were determined by HR-FAB-MS, 1D- and 2D-NMR spectral data, and enzymatic hydrolysis. Bacillus megaterium hydroxylated and glucosidated 1 to yield ent-7alpha,16beta-dihydroxybeyeran-19-oic acid ( 2), ent-16beta-hydroxybeyeran-19-oic acid alpha- D-glucopyranosyl ester ( 3), and ent-7alpha,16beta-dihydroxybeyeran-19-oic acid alpha- D-glucopyranosyl ester ( 4). Aspergillus niger hydroxylated 1 to yield ent-1beta,7alpha,16beta-trihydroxybeyeran-19-oic acid ( 5) and ent-1beta,7alpha-dihydroxy-16-oxobeyeran-19-oic acid ( 6). Metabolites 3 - 5 were characterized as new compounds. In addition, 2, 3, 5, and 6 were tested for antihypertensive effects, and we found that 5 and 6 were more potent than the parent compound 1.
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------>authors2=Hsu FL
------>authors3=Cheng JT
------>authors4=Chang CH
------>authors5=Liu PC
------>authors6=Lin SJ
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------>authors=Yang LM
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------>updateTitle=Hydroxylation and glucosidation of ent-16beta-Hydroxybeyeran-19-oic acid by Bacillus megaterium and Aspergillus niger.
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------>publish_year=2004
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A B C D E F G H I J K L M N O P Q R S T U V W X Y Z