Dihydrokaempferide

Dihydrokaempferide
Names
	IUPAC name 3,5,7-trihydroxy-2-(4-methoxyphenyl)-2,3-dihydrochromen-4-one
Identifiers
CAS Number	3570-69-2 ;
3D model (JSmol)	Interactive image;
ChemSpider	10305947 ;
PubChem CID	586387;
UNII	9V3SE2M92C ;
CompTox Dashboard (EPA)	DTXSID60929743 ;
	InChI InChI=1S/C16H14O6/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/h2-7,15-18,20H,1H3/t15-,16+/m0/s1 Key: CKDYDMSDCNQHEB-JKSUJKDBSA-N ;
	SMILES COc1ccc(cc1)[C@@H]2[C@H](C(=O)c3c(cc(cc3O2)O)O)O;
Properties
Chemical formula	C16H14O6
Molar mass	302.27 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Dihydrokaempferide is a flavanonol, a type of flavonoid. It can be found in Prunus domestica^[1] (plum tree), in the wood of Salix caprea^[2] (goat willow) and in the Brazilian green propolis.^[3]

References

^ Parmar, Virinder S.; Vardhan, Anand; Nagarajan, G.R.; Jain, Rajni (1992). "Dihydroflavonols from Prunus domestica". Phytochemistry. 31 (6): 2185–6. doi:10.1016/0031-9422(92)80399-Y. INIST 4305555.
^ Malterud, Karl E.; Bremnes, Torgunn E.; Faegri, Agnete; Moe, Turid; Dugstad, Eva K. Sandanger; Anthonsen, Thorleif; Henriksen, Liv M. (1985). "Flavonoids from the Wood of Salix caprea as Inhibitors of Wood-Destroying Fungi". Journal of Natural Products. 48 (4): 559–63. doi:10.1021/np50040a007. INIST 8569626.
^ Maruyama, Hiroe; Sumitou, Yoshiki; Sakamoto, Takashi; Araki, Yoko; Hara, Hideaki (2009). "Antihypertensive Effects of Flavonoids Isolated from Brazilian Green Propolis in Spontaneously Hypertensive Rats". Biological & Pharmaceutical Bulletin. 32 (7): 1244–50. doi:10.1248/bpb.32.1244. PMID 19571393. INIST 21802341.

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