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Pinobanksin

Names
IUPAC name (2R,3R)-3,5,7-Trihydroxyflavan-4-one
Systematic IUPAC name (2R,3R)-3,5,7-Trihydroxy-2-phenyl-2,3-dihydro-4H-1-benzopyran-4-one
Other names 3,5,7-trihydroxy-2-phenyl-2,3-dihydro-4H-chromen-4-one
Identifiers
CAS Number	548-82-3 Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:28103 N
ChEMBL	ChEMBL608410 Y
ChemSpider	65962 Y
KEGG	C09826
PubChem CID	73202
UNII	BK3ABR33DT Y
CompTox Dashboard (EPA)	DTXSID10203287
InChI InChI=1S/C15H12O5/c16-9-6-10(17)12-11(7-9)20-15(14(19)13(12)18)8-4-2-1-3-5-8/h1-7,14-17,19H/t14-,15+/m0/s1 Y Key: SUYJZKRQHBQNCA-LSDHHAIUSA-N Y InChI=1/C15H12O5/c16-9-6-10(17)12-11(7-9)20-15(14(19)13(12)18)8-4-2-1-3-5-8/h1-7,14-17,19H/t14-,15+/m0/s1 Key: SUYJZKRQHBQNCA-LSDHHAIUBG
SMILES O=C2c3c(O[C@H](c1ccccc1)[C@H]2O)cc(O)cc3O
Properties
Chemical formula	C15H12O5
Molar mass	272.25 g/mol
Density	1.497 g/mL
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

Pinobanksin is an antioxidant bioflavonoid (specifically a flavanonol, a category of flavonol) that inhibits peroxidation of low density lipoprotein and it has electron donor properties reducing alpha-tocopherol radicals.^{[citation needed]} It is present in sunflower honey.^[1]

Pinobanksin is biosynthesized from pinocembrin.

References

External links

• Media related to Pinobanksin at Wikimedia Commons