Sakuranetin

Sakuranetin

Names
IUPAC name (2S)-4′,5-Dihydroxy-7-methoxyflavan-4-one
Systematic IUPAC name (2S)-5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxy-2,3-dihydro-4H-1-benzopyran-4-one
Other names Naringenin 7-methyl ether
Identifiers
CAS Number	2957-21-3 Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:28927 N
ChEMBL	ChEMBL448297 N
ChemSpider	66249 N
ECHA InfoCard	100.019.073
IUPHAR/BPS	412
PubChem CID	73571
UNII	3O38P61299 Y
CompTox Dashboard (EPA)	DTXSID10874774
InChI InChI=1S/C16H14O5/c1-20-11-6-12(18)16-13(19)8-14(21-15(16)7-11)9-2-4-10(17)5-3-9/h2-7,14,17-18H,8H2,1H3/t14-/m0/s1 N Key: DJOJDHGQRNZXQQ-AWEZNQCLSA-N N InChI=1/C16H14O5/c1-20-11-6-12(18)16-13(19)8-14(21-15(16)7-11)9-2-4-10(17)5-3-9/h2-7,14,17-18H,8H2,1H3/t14-/m0/s1 Key: DJOJDHGQRNZXQQ-AWEZNQCLBK
SMILES COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O
Properties
Chemical formula	C16H14O5
Molar mass	286.27 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

Sakuranetin is a flavan-on, the 7-methoxy derivative of naringenin, found in Polymnia fruticosa^[1] and rice, where it acts as a phytoalexin against spore germination of Pyricularia oryzae.^[2]

Glycosides

Sakuranin is the 5-O-glucoside of sakuranetin.^{[citation needed]}

Metabolism

biosynthesis

Naringenin 7-O-methyltransferase uses naringenin to yield sakuranetin, with S-adenosyl-methionine as the methyl donor.^[3]

biodegradation

In compounds like 7-methoxylated flavanones like sakuranetin, demethylation followed by sulfation occur in model organism Cunninghamella elegans.^[4]

References

This article about an aromatic compound is a stub. You can help Wikipedia by expanding it.

• v
• t
• e

This page was last edited on 7 May 2023, at 00:40