Chrysosplenetin

Chrysosplenetin
Chemical structure of chrysosplenetin
Names
IUPAC name
4′,5-Dihydroxy-3,3′,6,7-tetramethoxyflavone
Systematic IUPAC name
5-Hydroxy-4-(4-hydroxy-3-methoxyphenyl)-3,6,7-trimethoxy-4H-1-benzopyran-4-one
Other names
Chrysosplenetin B
3,6,7,3'-Tetra-methylquercetagetin
Quercetagetin 3,6,7,3'-tetramethyl ether
Identifiers
CAS Number
  • 69234-29-3 checkY
  • 603-56-5 ☒N
3D model (JSmol)
  • Interactive image
ChemSpider
  • 4444927 ☒N
PubChem CID
  • 5281608
UNII
  • 9AA5Z8PMYE checkY
CompTox Dashboard (EPA)
  • DTXSID80975707 Edit this at Wikidata
InChI
  • InChI=1S/C19H18O8/c1-23-11-7-9(5-6-10(11)20)17-19(26-4)16(22)14-12(27-17)8-13(24-2)18(25-3)15(14)21/h5-8,20-21H,1-4H3 ☒N
    Key: NBVTYGIYKCPHQN-UHFFFAOYSA-N ☒N
  • InChI=1/C19H18O8/c1-23-11-7-9(5-6-10(11)20)17-19(26-4)16(22)14-12(27-17)8-13(24-2)18(25-3)15(14)21/h5-8,20-21H,1-4H3
    Key: NBVTYGIYKCPHQN-UHFFFAOYAO
  • O=C1c3c(O)c(OC)c(OC)cc3O/C(=C1/OC)c2ccc(O)c(OC)c2
Properties
Chemical formula
C19H18O8
Molar mass 374.345 g·mol−1
Density 1.448 g/mL
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references
Chemical compound

Chrysosplenetin is an O-methylated flavonol. It can be found in the root of Berneuxia thibetica and in Chamomilla recutita.[1]

References

  1. ^ Miroslav Repčák, Vanda Švehlı́ková, Ján Imrich, Kalevi Pihlaja (1999). "Jaceidin and chrysosplenetin chemotypes of Chamomilla recutita (L.) Rauschert". Biochemical Systematics and Ecology. 27 (7): 727–732. doi:10.1016/S0305-1978(98)00124-0.{{cite journal}}: CS1 maint: multiple names: authors list (link)
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Flavonols and their conjugates
Backbone
Aglycones
  • 3-Hydroxyflavone (synthetic) and derivatives
Flavonols
Aglycones
Conjugates
Glycosides of herbacetin
Glycosides of kaempferol
  • Afzelin (Kaempferol 3-rhamnoside)
  • Astragalin (kaempferol 3-O-glucoside)
  • Kaempferitrin (kaempferol 3,7-dirhamnoside)
  • Juglanin (Kaempferol 3-O-arabinoside)
  • Kaempferol 3-alpha-L-arabinopyranoside
  • Kaempferol 3-alpha-D-arabinopyranoside
  • Kaempferol 7-alpha-L-arabinoside
  • Kaempferol 7-O-glucoside
  • Kaempferol 3-lathyroside
  • Kaempferol 4'-rhamnoside
  • Kaempferol 5-rhamnoside
  • Kaempferol 7-rhamnoside
  • Kaempferol 7-O-alpha-L-rhamnofuranoside
  • Kaempferol 3-xyloside
  • Kaempferol 7-xyloside
  • Robinin (kaempferol-3-O-robinoside-7-O-rhamnoside)
  • Kaempferol 3-O-rutinoside
  • Sophoraflavonoloside (Kaempferol 3-O-sophoroside)
  • Trifolin (Kaempferol 3-O-beta-D-galactoside)
Glycosides of myricetin
Conjugates of quercetin
Sulfates
Glycosides
O-Methylated flavonols
Aglycones
Glycosides
of isorhamnetin
  • Narcissin (Isorhamnetin 3-O-rutinoside)
  • Isorhamnetin 3-O-glucoside
  • Tamarixetin 7-rutinoside
other
  • Azalein (Azaleatin 3-O-α-L-rhamnoside)
  • Centaurein (Centaureidin 7-O-glucoside)
  • Eupalin (Eupalitin 3-0-rhamnoside)
  • Eupatolin (Eupatolitin 3-O-rhamnoside)
  • Jacein (Jaceidin 7-O-glucoside)
  • Patulitrin (Patuletin 7-O-glucoside
  • Xanthorhamnin (Rhamnetin glycoside)
Derivative flavonols
Aglycones
  • Noricaritin
  • Dihydronoricaritin
Glycosides
  • Amurensin
  • Icariin
  • Phelloside
  • Dihydrophelloside
  • Rutin S
Pyranoflavonols
Aglycones
Furanoflavonols
Aglycones
Glycosides
  • Pongamoside A, B and C
Semisynthetic
Glycosides
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