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Icariin

From Wikipedia, the free encyclopedia
Not to be confused withIcaridin.
Icariin
Names
IUPAC name
7-(β-D-Glucopyranosyloxy)-5-hydroxy-4′-methoxy-8-(3-methylbut-2-en-1-yl)-3-(α-L-rhamnopyranosyloxy)flavone
Systematic IUPAC name
5-Hydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-en-1-yl)-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-4H-1-benzopyran-4-one
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard100.107.649Edit this at Wikidata
UNII
  • InChI=1S/C33H40O15/c1-13(2)5-10-17-19(45-33-28(42)26(40)23(37)20(12-34)46-33)11-18(35)21-24(38)31(48-32-27(41)25(39)22(36)14(3)44-32)29(47-30(17)21)15-6-8-16(43-4)9-7-15/h5-9,11,14,20,22-23,25-28,32-37,39-42H,10,12H2,1-4H3/t14-,20+,22-,23+,25+,26-,27+,28+,32-,33+/m0/s1 checkY
    Key: TZJALUIVHRYQQB-XLRXWWTNSA-N checkY
  • InChI=1/C33H40O15/c1-13(2)5-10-17-19(45-33-28(42)26(40)23(37)20(12-34)46-33)11-18(35)21-24(38)31(48-32-27(41)25(39)22(36)14(3)44-32)29(47-30(17)21)15-6-8-16(43-4)9-7-15/h5-9,11,14,20,22-23,25-28,32-37,39-42H,10,12H2,1-4H3/t14-,20+,22-,23+,25+,26-,27+,28+,32-,33+/m0/s1
    Key: TZJALUIVHRYQQB-XLRXWWTNBA
  • O=C3C(\O[C@@H]1O[C@H]([C@H](O)[C@@H](O)[C@H]1O)C)=C(/Oc4c(c(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc(O)c34)C\C=C(/C)C)c5ccc(OC)cc5
Properties
C33H40O15
Molar mass676.668 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

Icariin is achemical compound classified as aprenylatedflavonolglycoside, a type offlavonoid. It is the 8-prenyl derivative ofkaempferol 3,7-O-diglucoside. The compound has been isolated from several species of plant belonging to the genusEpimedium which are commonly known as horny goat weed, Yin Yang Huo,[1] andHerba epimedii.[2] Extracts from these plants produceaphrodisiac effects, and are used intraditional Chinese medicine to enhance erectile function.[3]

References

[edit]
  1. ^Liu JJ, Li SP, Wang YT (2006). "Optimization for quantitative determination of four flavonoids in Epimedium by capillary zone electrophoresis coupled with diode array detection using central composite design".J Chromatogr A.1103 (2):344–349.doi:10.1016/j.chroma.2005.11.036.PMID 16337210.
  2. ^Cai WJ, Huang JH, Zhang SQ, Wu B, Kapahi P, Zhang XM, Shen ZY (2011). Blagosklonny MV (ed.)."Icariin and its derivative icariside II extend healthspan via insulin/IGF-1 pathway in C. elegans".PLOS ONE.6 (12) e28835.Bibcode:2011PLoSO...628835C.doi:10.1371/journal.pone.0028835.PMC 3244416.PMID 22216122.
  3. ^Makarova MN, Pozharitskaya ON, Shikov AN, Tesakova SV, Makarov VG, Tikhonov VP (2007). "Effect of lipid-based suspension ofEpimedium koreanum Nakai extract on sexual behavior in rats".J Ethnopharmacol.114 (3):412–416.doi:10.1016/j.jep.2007.08.021.PMID 17890032.
PDE1
PDE2
PDE3
PDE4
PDE5
PDE7
PDE9
PDE10
PDE11
Non-selective
Unsorted
Flavonols and their conjugates
Backbone
Aglycones
Flavonols
Aglycones
Conjugates
Glycosides ofherbacetin
Glycosides ofkaempferol
Glycosides ofmyricetin
Conjugates ofquercetin
Sulfates
Glycosides
O-Methylated flavonols
Aglycones
Glycosides
of isorhamnetin
other
Derivative flavonols
Aglycones
Glycosides
Pyranoflavonols
Aglycones
Furanoflavonols
Aglycones
Glycosides
Semisynthetic
Glycosides
Retrieved from "https://en.wikipedia.org/w/index.php?title=Icariin&oldid=1329515083"
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