17650-84-9

Usage

Uses

Used in Pharmaceutical Industry:
KAEMPFEROL-3-O-RUTINOSIDE is used as a pharmaceutical agent for its antioxidant and anti-diabetic properties. It has been found to display potential anti-diabetic activity, making it a valuable compound for the development of treatments for diabetes.
Used in Nutraceutical Industry:
KAEMPFEROL-3-O-RUTINOSIDE is used as a nutraceutical ingredient for its antioxidant properties. Its ability to scavenge free radicals, such as DPPH and ABTS radicals, contributes to its potential use in the development of supplements and functional foods that promote overall health and well-being.
Used in Cosmetic Industry:
KAEMPFEROL-3-O-RUTINOSIDE is used as an active ingredient in the cosmetic industry for its antioxidant and skin-protective properties. Its ability to neutralize free radicals and protect skin cells from oxidative stress makes it a valuable component in skincare products aimed at promoting skin health and preventing premature aging.
Used in Agricultural Industry:
KAEMPFEROL-3-O-RUTINOSIDE is used as a natural pesticide or growth promoter in the agricultural industry. Its antioxidant properties can help protect plants from environmental stressors, such as UV radiation and oxidative damage, leading to improved crop yields and overall plant health.

InChI: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

Upstream product

• 131573-90-5 kaempferol 3-O-(2^G-xylosylrutinoside) 
• 34336-18-0 7-O-β-D-glucopyranosyloxy-4',5-dihydroxy-3-[O-α-L-rhamnopyranosyl-(1->6)-3-O-β-D-glucopyranosyloxy]flavone 
• 131573-90-5 kaempferol 3-O-β-D-<2^G-O-β-D-xylopyranosyl-6^G-O-α-L-rhamnopyranosyl>glucopyranoside 
• 57526-56-4 kaempherol 3-O-[α-L-rhamnopyranosyl-(1->6)]-β-D-glucopyranosyl-7-O-α-L-rhamnopyranoside 
• 131559-51-8 kaempferol 3-O-(2^G-xylosylrutinoside)-7-O-glucoside 
• 135095-52-2 3-O-[(2-O-β-D-galactopyranosyl-6-O-α-L-rhamnopyranosyl)-β-D-glucopyranosyl]-kaempferol 
• 131559-50-7 kaempferol 3-O-(2^G-glucosylrutinoside)-7-O-glucoside 

Downstream Products

• 33978-17-5 pelargonidin 3-O-β-rutinoside 
• 2280-44-6 D-Glucose 
• 520-18-3 kaempferol 
• 73-34-7 D-rhamnose 
• 26184-96-3 rutinose 
• 552-74-9 6-O-α-L-rhamnopyranosyl-β-D-glucopyranose 
• 3615-41-6 L-Rhamnose 
• 50-99-7 D-glucose 
• 4205-23-6 D-gulose 
• 634-74-2 D-rhamnose 
• 58947-55-0 biorobin nonaacetate 
• 1318780-82-3 C₃₀H₁₈O₁₃ 
• 61198-83-2 1,2,3,4-tetra-O-benzoyl-6-desoxy-α-L-mannopyranose 

Relevant academic research and scientific papers

Kaempferol and its glycosides from Equisetum silvaticum L. from the khanty-mansi autonomous area

Three flavonoids were isolated from the aerial part of the wood horsetail (Equisetum silvaticum L.); two of them were found for the first time. The compounds were identified as kaempferol, kaempferol 3-O-β-D-galactopyranosyl-7-O-α-L-rhamnopyranoside and kaempferol 3-O-rutinosyl-7-O-L-rhamnopyranoside on the basis of the chemical transformations and IR, UV, 1H-NMR and mass spectra.

Method For Preparing Kaempferol-3-0-Rutinoside and Composition of Skin External Application Comprising Thereof

Disclosed is a method for the preparation of kaempferol-3-O-rutinoside and a composition of a skin external application comprising kaempferol-3-O-rutinoside as an active ingredient. The method for isolating kaempferol-3-O-rutinoside through hydrolysis uses an enzyme or microbe that removes the sugar selectively from kaempferol-3-O-rutinoside glycosides in a plant extract. Disclosed also is a composition of a skin external application comprising kaempferol-3-O-rutinoside that prevents skin wrinkle.

Two flavonol glycosides from seeds of Camellia sinensis.

Two novel flavonol triglycosides, camelliaside A and B, have been isolated from seeds of Camellia sinensis. The structures were determined to be kaempferol 3-O-[2-O-beta-D- galactopyranosyl-6-O-alpha-L-rhamnopyranosyl]-beta-D-glucopyranoside and kaempferol 3-O-[2-O-beta- D-xylopyranosyl-6-O-alpha-L-rhamnopyranosyl]-beta-D-glucopyranoside on the basis of spectroscopic, chemical and enzymatic studies. These types of interglycosidic linkages, Gal(1----2)[Rha(1----6)]Glc and Xyl(1----2)[Rha(1----6)]Glc, have not been reported previously in flavone and flavonol glycosides.

KAEMPFEROL GLYCOSIDES FROM HOSTA VENTRICOSA

Leaves of Hosta ventricosa yielded eight kaempferol glycosides, of which six: the 3-(2G-glucosylrutinoside)-7-glucoside, 3-sophoroside-7-glucoside, 3-rutinoside-7-glucoside, 3-(2G-glucosylrutinoside), 3-sophoroside, 3-rutinoside were fully characterized and two: 3-xylosylrutinoside-7-glucoside and 3-xylosylrutinoside were tentatively identified.Investigations included 1H-1H-COSY and 1H-1H 2D J NMR analysis.

Constituents of Cupuliferae, II. - A New Acylated Flavonoid Glycoside from Castanea sativa Mill.

From leaves of Castanea sativa Mill. in addition to tiliroside , 3>, a new acylated flavonoid glycoside has been isolated and identified as kaempferol 3-O-Glc-(p-coumaroyl)-α-L-rhamnopyranosyl-(1->6)-β-D-glucopyranoside> (1).

The final structure of robinin and biorobin and their total synthesis

Robinin has been proved by total synthesis and by methylation analysis using GC-MS to be kaempferol-3- O-(6-O-α-l-rhamnopyranosyl -β-d-galactopyranoside)-7-O-α-l-rhamnopyranoside and not, as claimed by Maksjutina et al., a mixture of 4 glycosides containing the 7-O-rhamnosyl moiety in the α- and β-furanoside as well as in the α- and β-pyranoside forms. The assumption that the 3-O-rhamnosido -galactose moiety contained furanoid rings was also disproved.