Alpinetin

Alpinetin
Names

IUPAC name (2S)-7-Hydroxy-5-methoxy-2-phenyl-2,3-dihydro-4H-chromen-4-one
Identifiers
CAS Registry Number	36052-37-6^N
ChEBI	CHEBI:449909^N
ChEMBL	ChEMBL537954^N
ChemSpider	135938^Y
InChI InChI=1S/C16H14O4/c1-19-14-7-11(17)8-15-16(14)12(18)9-13(20-15)10-5-3-2-4-6-10/h2-8,13,17H,9H2,1H3/t13-/m0/s1^Y Key: QQQCWVDPMPFUGF-ZDUSSCGKSA-N^Y InChI=1S/C16H14O4/c1-19-14-7-11(17)8-15-16(14)12(18)9-13(20-15)10-5-3-2-4-6-10/h2-8,13,17H,9H2,1H3/t13-/m0/s1
Jmol-3D images	Image
PubChem	154279
SMILES O=C2c3c(O[C@H](c1ccccc1)C2)cc(O)cc3OC
Properties
Molecular formula	C₁₆H₁₄O₄
Molar mass	270.28 g·mol⁻¹
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
N verify (what is: Y/N?)
Infobox references

Alpinetin is a phytochemical isolated from a variety of plants including those of the genus Alpinia.^[1] It is going through tests to see if it is a vasorelaxant.

References

↑ Kimura, Yushiro; Takahashi, Shuhichi; Yoshida, Ikuo (1968). "Constituents of Alpinia. XII. Constituents of the seeds of A. katsumadai. I. The structure of cardamomin". Yakugaku Zasshi 88 (2): 239–241. PMID 5692492.

External links

Flavanones and their glycosides

Flavanones	Butin Eriodictyol Naringenin Pinocembrin

O-methylated flavanones	Alpinetin Hesperetin Homoeriodictyol Isosakuranetin Pinostrobin (Pinocembrin-7-methylether) Sakuranetin Sterubin

C-methylated flavanones	Poriol

Glycosides	Eriocitrin Neoeriocitrin Hesperidin Liquiritin Naringin (Narigenin 7-O-neohesperidoside) Narirutin (Naringenin 7-O-rutinoside) Poncirin Prunin (Naringenin-7-O-glucoside) Sakuranin

Acetylated	8-Prenylnaringenin Isoxanthohumol Sophoraflavanone G

Acetylated glycosides	Nirurin