Kaempferol 3-O -rutinoside Names IUPAC name 7-[(2S ,3R ,4S ,5S ,6R )-4,5-Dihydroxy-6-(hydroxymethyl)-3-[(2S ,3R ,4R ,5R ,6S )-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,5-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one
Other names Kaempferol 3-
O -
rutinoside Kaempferol 3-
O -rhamnosyl-glucoside
Nicotiflorin
Kaempferol-3-
O -β-
D -glucopyranoside-7-
O -α-
L -rhamnopyranoside
Kaempferol 7-neohesperidoside
Identifiers ChEBI ChemSpider ECHA InfoCard 100.211.421 EC Number KEGG UNII InChI=1S/C27H30O15/c1-9-17(31)20(34)22(36)26(39-9)38-8-15-18(32)21(35)23(37)27(41-15)42-25-19(33)16-13(30)6-12(29)7-14(16)40-24(25)10-2-4-11(28)5-3-10/h2-7,9,15,17-18,20-23,26-32,34-37H,8H2,1H3/t9-,15+,17-,18+,20+,21-,22+,23+,26+,27-/m0/s1
Key: RTATXGUCZHCSNG-QHWHWDPRSA-N
InChI=1/C27H30O15/c1-9-17(31)20(34)22(36)26(39-9)38-8-15-18(32)21(35)23(37)27(41-15)42-25-19(33)16-13(30)6-12(29)7-14(16)40-24(25)10-2-4-11(28)5-3-10/h2-7,9,15,17-18,20-23,26-32,34-37H,8H2,1H3/t9-,15+,17-,18+,20+,21-,22+,23+,26+,27-/m0/s1
Key: RTATXGUCZHCSNG-QHWHWDPRBU
C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)Oc3c(=O)c4c(cc(cc4oc3c5ccc(cc5)O)O)O)O)O)O)O)O)O
Properties C27 H30 O15 Molar mass 594.52 g/mol Density 1.762 g/mL Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Kaempferol-3-O -rutinoside is a bitter-tasting flavonol glycoside . It can be isolated from the rhizomes of the fern Selliguea feei .[ 1]
References ^ Baek, Nam-In; Kennelly, Edward J.; Kardono, Leonardus B.S.; Tsauri, Soefjan; Padmawinata, Kosasih; Doel Soejarto, D.; Douglas Kinghorn, A. (1994). "Flavonoids and a proanthocyanidin from rhizomes of Selliguea feei". Phytochemistry . 36 (2): 513– 518. doi :10.1016/S0031-9422(00)97105-X . INIST 3300075
External links
Flavonols and their conjugates
Backbone
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) Sophoraflavonoloside (Kaempferol 3-O-sophoroside) Trifolin (Kaempferol 3-O-beta-D-galactoside) Glycosides of myricetin Conjugates of quercetin
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
Pyranoflavonols
Furanoflavonols
Semisynthetic