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Microbiological Transformation of Chromone, Chromanone, and Ring A Hydroxyflavones
- Source :
- Journal of Natural Products. 53:1471-1478
- Publication Year :
- 1990
- Publisher :
- American Chemical Society (ACS), 1990.
-
Abstract
- Microbial transformation of chromone, chromanone, and 3 ring A hydroxyflavones (5-hydroxy-, 6-hydroxy-, and 7-hydroxyflavones) was attempted using thirty-two microorganisms. While chromone was not biotransformed, chromanone was transformed to chromone and chromanol by Aspergillus niger in 2% yield. Ring A hydroxylated flavones were transformed to the corresponding C-4' hydroxylated metabolites, and the yields and rate of product formation were found to correlate with the distance between the C-4 carbonyl group and the hydroxyl group in ring A.
- Subjects :
- Magnetic Resonance Spectroscopy
Stereochemistry
Flavonoid
Pharmaceutical Science
Hydroxylation
Ring (chemistry)
Flavones
Analytical Chemistry
chemistry.chemical_compound
Drug Discovery
Biotransformation
Flavonoids
Pharmacology
chemistry.chemical_classification
Bacteria
biology
Organic Chemistry
Aspergillus niger
Fungi
Nuclear magnetic resonance spectroscopy
biology.organism_classification
Complementary and alternative medicine
chemistry
Chromones
Yield (chemistry)
Chromone
Molecular Medicine
Subjects
Details
- ISSN :
- 15206025 and 01633864
- Volume :
- 53
- Database :
- OpenAIRE
- Journal :
- Journal of Natural Products
- Accession number :
- edsair.doi.dedup.....5b9bfbc6af41078cad58cea592960990
- Full Text :
- https://doi.org/10.1021/np50072a011