
doi: 10.1248/cpb.55.682
pmid: 17409573
The microbial transformation of a steroidal alkaloid, dictyophlebine (1) with Rhizopus stolonifer (ATCC 10404) afforded three oxidized metabolites 2-4. Compound 2 was found to be a new product. These metabolites were structurally characterized on the basis of modern spectroscopic techniques. Their inhibitory activity towards acetyl- and butyrylcholinesterase has been evaluated and the new product 2 has been found to be more potent than the parent compound and other metabolites.
Spectrometry, Mass, Electrospray Ionization, Magnetic Resonance Spectroscopy, <i>Rhizopus stolonifer</i>, dictyophlebine, Spectrophotometry, Ultraviolet, Steroids, oxidized metabolite, cholinesterase inhibition, Rhizopus stolonifer, Biotransformation, Rhizopus
Spectrometry, Mass, Electrospray Ionization, Magnetic Resonance Spectroscopy, <i>Rhizopus stolonifer</i>, dictyophlebine, Spectrophotometry, Ultraviolet, Steroids, oxidized metabolite, cholinesterase inhibition, Rhizopus stolonifer, Biotransformation, Rhizopus
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