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Open Access Articles- Top Results for Prunetin

Prunetin

Prunetin
Chemical structure of prunetin
Prunetin molecule
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IUPAC name
5-hydroxy-3-(4-hydroxyphenyl)-7-methoxychromen-4-one
Other names
Prunusetin
4',5-dihydroxy-7-methoxyisoflavone
5,4'-dihydroxy-7-methoxyisoflavone
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552-59-0 7pxY=
ChEBI CHEBI:8600 7pxN
ChEMBL ChEMBL491174 7pxN
ChemSpider 4445116 7pxN
EC number 209-018-5
Jmol-3D images Image
KEGG C10521 7pxN
PubChem Template:Chembox PubChem/format
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C16H12O5
Molar mass 284.26 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

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).[1] Prunetin isolated from pea roots can act as an attractant for Aphanomyces euteiches zoospores.[2] It is also an allosteric inhibitor of human liver aldehyde dehydrogenase.[3]

Glycosides

References

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