Abstract:
:The enzymatic glucose cleavage of palicoside revealed the biosynthetic pathway to akagerine, whereas the conversion of dolichantoside led to a new quaternary heteroyohimbine alkaloid named N(b)-methyl-21-beta-hydroxy-mayumbine. The hypothetical models of reactions occurring after the conversion of both substrates are proposed. Dolichantoside and palicoside, as well as Strychnos mellodora stem bark crude ethanol extract, exhibit significant antimycotic activity against human pathogens in presence of specific glucosidase.
journal_name
Phytochemistryjournal_title
Phytochemistryauthors
Brandt V,Tits M,Penelle J,Frédérich M,Angenot Ldoi
10.1016/s0031-9422(01)00085-1subject
Has Abstractpub_date
2001-07-01 00:00:00pages
653-9issue
5eissn
0031-9422issn
1873-3700pii
S0031-9422(01)00085-1journal_volume
57pub_type
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