Weight | 284.267 g/mol |
---|---|
Formula | C16H12O5 |
Hydrogen Acceptors | 5 |
Hydrogen Donors | 2 |
Aromatic Rings | 3 |
Rotatable Bonds | 2 |
Prunetin (552-59-0)
5,4'-dihydroxy-7-methoxyisoflavone
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- Sigma-Aldrich - Prunetin83.40 - 328.00 USD
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- Disposition of flavonoids via enteric recycling: enzyme stability affects characterization of prunetin glucuronidation across species, organs, and UGT isoforms. (Molecular Pharmaceutics, 2007)
- Aphanomyces euteiches Zoospore Attractant Isolated from Pea Root; Prunetin (Japanese Journal of Phytopathology, 1986)
- A DFT study on the structural, electronic properties and radical scavenging mechanisms of calycosin, glycitein, pratensein and prunetin (Computational and Theoretical Chemistry, 2012)
- Inhibition of secretion, production and gene expression of mucin from cultured airway epithelial cells by prunetin. (Phytotherapy Research, 2011)
- Molecular mechanisms underlying the anti-obesity potential of prunetin, an O-methylated isoflavone (Biochemical Pharmacology, 2013)
- Allosteric inhibition of human liver aldehyde dehydrogenase by the isoflavone prunetin (Biochemical Pharmacology, 1997)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 5,4'-dihydroxy-7-methoxyisoflavone
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SMILESCOC1=CC(=C2C(=C1)OC=C(C2=O)C3=CC=C(C=C3)O)O
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InChIKeyKQMVAGISDHMXJJ-UHFFFAOYSA-N
- Pubchem - Prunetin
- Wikipedia - prunetin
Prunetin is an O-methylated isoflavone, a type of flavonoid. It has been isolated for the first time by Finnemore in 1910 in the bark of Prunus emarginata (the Oregon cherry). Prunetin isolated from pea roots can act as an attractant for Aphanomyces euteiches zoospores.
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