Kaempferitrin

Kaempferitrin
Kaempferitrin structure
Names
IUPAC name
4′,5-Dihydroxy-3,7-bis(α-L-rhamnopyranosyloxy)flavone
Systematic IUPAC name
5-Hydroxy-2-(4-hydroxyphenyl)-3,7-bis{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-4H-1-benzopyran-4-one
Other names
Lespenefril
Lespenephryl
Lespedin
lespenephril
Kaempferol 3,7-dirhamnoside
Kaempferol 3,7 bisrhamnoside
Identifiers
CAS Number
  • 482-38-2 checkY=  checkY=  checkY
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:68883
ChEMBL
  • ChEMBL251766 checkY=  checkY=  checkY=  checkY=  checkY=  checkY
ChemSpider
  • 4588900
KEGG
  • C16981
PubChem CID
  • 5486199
UNII
  • VPV01U3R59 checkY
CompTox Dashboard (EPA)
  • DTXSID90197458 Edit this at Wikidata
  • CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)O)O)O)C5=CC=C(C=C5)O)O)O)O)O
Properties
Chemical formula
C27H30O14
Molar mass 578.52 g/mol
Density 1.7 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

Kaempferitrin is a chemical compound. It can be isolated from the leaves of Hedyotis verticillata[1] and from Onychium japonicum.[2]

Kaempferitrin is the 3,7-dirhamnoside of kaempferol.

References

  1. ^ Hamzah, Ahmad Sazali; Lajis, Nordin H.; Sargent, M. V. (1994). "Kaempferitrin from the leaves of Hedyotis verticillata and its biological activity". Planta Medica. 60 (4): 388–389. doi:10.1055/s-2006-959513. PMID 7938277. S2CID 42952045. INIST 3324508.
  2. ^ Kobayashi, Kenji (1944). "Tachi shinobu no ichi seibun Kaempferol-birhamnosid ni shūte" [On kaempferol dirhamnoside, one component of carrot fern]. Yakugaku zasshi (in Japanese). 64 (9): 35. doi:10.1248/yakushi1944a.64.9_35a. S2CID 100133209.
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Flavonols and their conjugates
Backbone
Aglycones
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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