Abstract
The isolation procedure for obtaining a new nuphar alkaloid, 6,6'-dihydroxythiobinupharidine (formerly named 6,6'- dihydroxythionuphlutine-A), and its in vitro activity against eight human pathogenic fungi are described. The isolation procedure for obtaining a new nuphar alkaloid, 6,6'-dihydroxythiobinupharidine (formerly named 6,6'- dihydroxythionuphlutine-A), and its in vitro activity against eight human pathogenic fungi are described.
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