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