Kaempferide

Names
IUPAC name 3,5,7-Trihydroxy-4′-methoxyflavone
Systematic IUPAC name 3,5,7-Trihydroxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one
Other names Kaempferid 4′-Methylkaempferol Kaempferol 4′-methyl ether 4′-O-Methylkaempferol
Identifiers
CAS Number	491-54-3 Y
3D model (JSmol)	Interactive image Interactive image
ChEBI	CHEBI:6099 N
ChEMBL	ChEMBL40919 N
ChemSpider	4444985 N
ECHA InfoCard	100.007.036
KEGG	C10098 N
PubChem CID	5281666
UNII	508XL61MPD Y
CompTox Dashboard (EPA)	DTXSID9034155
InChI InChI=1S/C16H12O6/c1-21-10-4-2-8(3-5-10)16-15(20)14(19)13-11(18)6-9(17)7-12(13)22-16/h2-7,17-18,20H,1H3 N Key: SQFSKOYWJBQGKQ-UHFFFAOYSA-N N InChI=1/C16H12O6/c1-21-10-4-2-8(3-5-10)16-15(20)14(19)13-11(18)6-9(17)7-12(13)22-16/h2-7,17-18,20H,1H3 Key: SQFSKOYWJBQGKQ-UHFFFAOYAC
SMILES COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O
Properties
Chemical formula	C16H12O6
Molar mass	300.26 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

Kaempferide is an O-methylated flavonol, a type of chemical compound. It can be found in Kaempferia galanga (aromatic ginger). It has been noted to inhibit pancreatic cancer growth by blockading an EGFR-related pathway.^[1]

Metabolism[edit]

The enzyme kaempferol 4'-O-methyltransferase uses S-adenosyl-L-methionine and kaempferol to produce S-adenosyl-L-homocysteine and kaempferide.

Glycosides[edit]

Icariin is the tert-amyl alcohol derivative of kaempferide 3,7-O-diglycoside.

References[edit]

External links[edit]

• Kaempferide at the HMDB