(Q104394028)

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,4R,5S)-3,4,5-trihydroxy-6-[[(2R,4R,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

1 reference

kaempferol 3-robinobioside

1 reference

mass

594.15847026 dalton

1 reference

stereoisomer of

Kaempferol-3-rutinoside

2 references

2 references

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-({[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxan-2-yl]oxy}chromen-4-one

2 references

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

2 references

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

2 references

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

2 references

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

1 reference

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

1 reference

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

1 reference

kaempferol 3-robinobioside

1 reference

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

1 reference

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

1 reference

4',5,7-Trihydroxy-3-(6-O-beta-D-rhamnopyranosyl-beta-D-glucopyranosyloxy)flavone

1 reference

chemical formula

C₂₇H₃₀O₁₅

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canonical SMILES

O=C1C(OC2OC(COC3OC(C)C(O)C(O)C3O)C(O)C(O)C2O)=C(OC=4C=C(O)C=C(O)C14)C=5C=CC(O)=CC5

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isomeric SMILES

C[C@@H]1O[C@@H](OC[C@H]2O[C@@H](Oc3c(-c4ccc(O)cc4)oc4cc(O)cc(O)c4c3=O)[C@H](O)[C@@H](O)[C@H]2O)[C@H](O)[C@H](O)[C@H]1O

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found in taxon

Solidago virgaurea

1 reference

High-performance liquid chromatographic analysis of flavonol glycosides of Solidago virgaurea

Acalypha indica

1 reference

Flavonoids from Acalypha indica

Salvadora persica

1 reference

FLAVONOID GLYCOSIDES FROM THE LEAVES OF SALVADORA PERSICA L.

Atropanthe sinensis

1 reference

Flavonoids from some species of the genus Cucumis

Silphium perfoliatum

2 references

Kaempferol triosides from Silphium perfoliatum

Kaempferol triosides from Silphium perfoliatum

Strychnos variabilis

2 references

Flavonol glycosides from leaves of Strychnos variabilis

Flavonol glycosides from leaves of Strychnos variabilis

Oxytropis falcata

1 reference

3-Hydroxy-3-methylglutaryl flavonol glycosides from Oxytropis falcata

Chimarrhis turbinata

1 reference

New biflavonoid and other flavonoids from the leaves of Chimarrhis turbinata and their antioxidant activities

Sinoadina racemosa

1 reference

Flavonoid glycosides from Adina racemosa and their inhibitory activities on eukaryotic protein synthesis

Camellia sinensis

2 references

Medicinal flowers. XIV. New acylated oleanane-type triterpene oligoglycosides with antiallergic activity from flower buds of chinese tea plant (Camellia sinensis).

Medicinal flowers. XXII. Structures of chakasaponins V and VI, chakanoside I, and chakaflavonoside A from flower buds of Chinese tea plant (Camellia sinensis).

Cassytha filiformis

1 reference

Vasorelaxing alkaloids and flavonoids from Cassytha filiformis

Crotalaria trichotoma

1 reference

Crotalionosides A-C, three new megastigmane glucosides, two new pterocarpan glucosides and a chalcone C-glucoside from the whole plants of Crotalaria zanzibarica

Fraxinus americana

1 reference

Secoiridoid glucosides from Fraxinus americana

Glycine max

1 reference

Vascular effects of a soy leaves (Glycine max) extract and kaempferol glycosides in isolated rat carotid arteries.

Gymnema sylvestre

1 reference

Two new flavonol glycosides from Gymnema sylvestre and Euphorbia ebracteolata

Lysimachia mauritiana

1 reference

A flavonol glycoside from Lysimachia Mauritiana

Monteverdia ilicifolia

1 reference

Constituents from Maytenus ilicifolia leaves and bioguided fractionation for gastroprotective activity

Rhamnus disperma

1 reference

Polyphenolic metabolites of Rhamnus disperma

Styphnolobium japonicum

1 reference

Flavonol tetraglycosides and other constituents from leaves of Styphnolobium japonicum (Leguminosae) and related taxa

Nelumbo nucifera

1 reference

Simultaneous qualitative assessment and quantitative analysis of flavonoids in various tissues of lotus (Nelumbo nucifera) using high performance liquid chromatography coupled with triple quad mass spectrometry

Anthyllis lagascana

1 reference

Anthyllis henoniana

1 reference

Delphinium oliverianum

1 reference

Cytotoxic activities of flavonoid glycoside acetates from Consolida oliveriana

Ebenus sibthorpii

1 reference

Anthyllis subsimplex

1 reference

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

Identifiers

InChI

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InChIKey

RTATXGUCZHCSNG-KYGWAIEOSA-N

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CAS Registry Number

17297-56-2

1 reference

CAS (formerly Chemical Abstracts Service)

25 January 2022

1 reference

17 September 2022