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 (Q105245030)

kaempferol 3-robinobioside

1 reference

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

mass

594.15847026 dalton

1 reference

kaempferol 3-robinobioside

stereoisomer of

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

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

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-[(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

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

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

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

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

Kaempferol-3-rutinoside

1 reference

chemical formula

C₂₇H₃₀O₁₅

0 references

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

0 references

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

0 references

found in taxon

Alkanna orientalis

2 references

The Flavonoids of Alkanna orientalis

Antiviral Flavonoids fromAlkanna orientalis

Aristolochia kaempferi

1 reference

Aristofolin-A, a denitro-aristolochic acid glycoside and other constituents from Aristolochia kaempferi

Boehmeria holosericea

1 reference

Flavones and other compounds of Boehmeria tricuspis and B. Holosericea

Camellia sinensis

1 reference

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

Capparis spinosa

1 reference

108. The isolation of L-stachydrine from the fruit of Capparis tomentosa

Centaurea hierapolitana

1 reference

Elemanolide sesquiterpenes and eudesmane sesquiterpene glycosides from Centaurea hierapolitana

Clitoria ternatea

1 reference

Flavonoid composition related to petal color in different lines of Clitoria ternatea.

Colubrina asiatica

1 reference

New jujubogenin glycosides from Colubrina asiatica

Laennecia filaginoides

1 reference

Antiprotozoal activity of the constituents of Conyza filaginoides

Eucommia ulmoides

1 reference

Iridoids from the green leaves of Eucommia ulmoides

Euphorbia larica

1 reference

Chemistry and biological activity of secondary metabolites in Euphorbia from Iran

Euphorbia virgata

1 reference

Chemistry and biological activity of secondary metabolites in Euphorbia from Iran

Ginkgo biloba

1 reference

Coumaroyl flavonol glycosides from the leaves of Ginkgo biloba

Juniperus communis depressa

1 reference

Neolignan and flavonoid glycosides in Juniperus communis var. depressa

Marrubium velutinum

1 reference

Acylated flavonoid and phenylethanoid glycosides from Marrubium velutinum

Morinda citrifolia

3 references

Chemical constituents of the fruits of Morinda citrifolia (Noni) and their antioxidant activity.

Lipoxygenase inhibitory constituents of the fruits of noni (Morinda citrifolia) collected in Tahiti.

Chemical Constituents from the Stems of Morinda citrifolia Linn

Nyctanthes arbor-tristis

1 reference

Nyctanthosid, ein neues iridoid aus nyctanthes arbor-tristis L.

Pelargonium reniforme

1 reference

O-Galloyl-C-glycosylflavones from Pelargonium reniforme

Scorzonera divaricata

1 reference

Biologically active natural products from Mongolian medicinal plants Scorzonera divaricata and Scorzonera pseudodivaricata

Silphium perfoliatum

1 reference

Kaempferol triosides from Silphium perfoliatum

Solidago altissima

1 reference

New flavonoid glycosides from the leaves of Solidago altissima

Styphnolobium japonicum

2 references

Four new isoflavone triglycosides from Sophora japonica

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

Spermacoce laevis

1 reference

(Z)-3-Hexenyl diglycosides from Spermacoce laevis Roxb.

Strychnos spinosa

1 reference

Secoiridoid glucosides from Strychnos spinosa

Tordylium apulum

1 reference

Flavonoids and bioactive coumarins of Tordylium apulum

Juniperus communis var. depressa

1 reference

Neolignan and flavonoid glycosides in Juniperus communis var. depressa

Senna hirsuta var. hirsuta

1 reference

Flavonol glycosides from cassia hirsuta

Rhodiola rosea

1 reference

Neuraminidase inhibitory activities of flavonols isolated from Rhodiola rosea roots and their in vitro anti-influenza viral activities

Tribulus terrestris

1 reference

Flavonoid glycosides of Tribulus pentandrus and T. Terrestris

Phaseolus vulgaris

2 references

Composition and Content of Flavonol Glycosides in Green Beans and Their Fate during Processing

Antioxidant properties of flavonol glycosides from green beans

Foeniculum vulgare

2 references

Bioguided isolation and identification of the nonvolatile antioxidant compounds from fennel (Foeniculum vulgare Mill.) waste

Separation and characterization of phenolic compounds in fennel (Foeniculum vulgare) using liquid chromatography-negative electrospray ionization tandem mass spectrometry.

Humulus lupulus

1 reference

Metabolite profiling of flavonols and in vitro antioxidant activity of young shoots of wild Humulus lupulus L. (hop).

Carica papaya

1 reference

HPLC-based activity profiling for antiplasmodial compounds in the traditional Indonesian medicinal plant Carica papaya L.

Dianthus caryophyllus

2 references

Flavonoids from carnation (Dianthus caryophyllus) and their antifungal activity

Quantification of major flavonoids in carnation tissues (Dianthus caryophyllus) as a tool for cultivar discrimination.

Arabidopsis thaliana

1 reference

Identification of primary and secondary metabolites with phosphorus status-dependent abundance inArabidopsis, and of the transcription factor PHR1 as a major regulator of metabolic changes during phosphorus limitation

Capsella bursa-pastoris

1 reference

Chemical composition and biological screening of Capsella bursa-pastoris

soybean

1 reference

Soybean flavonol glycosides: identification and biochemical genetics

Morus alba

2 references

Characterization of the polyphenolic fraction of Morus alba leaves extracts by HPLC coupled to a hybrid IT-TOF MS system

The novel contributors of anti-diabetic potential in mulberry polyphenols revealed by UHPLC-HR-ESI-TOF-MS/MS.

Cymbopogon citratus

1 reference

Pterospartum tridentatum, Gomphrena globosa and Cymbopogon citratus: A phytochemical study focused on antioxidant compounds

Prunus avium

3 references

In-time and in-space tandem mass spectrometry to determine the metabolic profiling of flavonoids in a typical sweet cherry (Prunus avium L.) cultivar from Southern Italy

Chemical characterisation and bioactive properties of Prunus avium L.: The widely studied fruits and the unexplored stems

Analysis of glycosylated flavonoids extracted from sweet-cherry stems, as antibacterial agents against pathogenic Escherichia coli isolates.

Capsicum annuum

1 reference

Integrative analysis of metabolome and transcriptome reveals the mechanism of color formation in pepper fruit (Capsicum annuum L.).

Nicotiana tabacum

1 reference

Flavonoid and certain related phenolic compounds in parts of the tobacco flower

tomato

1 reference

A liquid chromatography-mass spectrometry-based metabolome database for tomato

potato

1 reference

Metabolite profiling of red and blue potatoes revealed cultivar and tissue specific patterns for anthocyanins and other polyphenols.

Scorzonera virgata

1 reference

Biologically active natural products from Mongolian medicinal plants Scorzonera divaricata and Scorzonera pseudodivaricata

Bruguiera sexangula

1 reference

Rhyncosides A-F, phenolic constituents from the Chinese mangrove plant Bruguiera sexangula var. rhynchopetala

Boehmeria japonica tenera

1 reference

Flavones and other compounds of Boehmeria tricuspis and B. Holosericea

Annona muricata

5 references

Novel cytotoxic annonaceous acetogenins from Annona muricata

New cytotoxic monotetrahydrofuran annonaceous acetogenins from Annona muricata

Five novel mono-tetrahydrofuran ring acetogenins from the seeds of Annona muricata

Cohibins C and D, two important metabolites in the biogenesis of acetogenins from Annona muricata and Annona nutans

Annona muricata (Annonaceae): A Review of Its Traditional Uses, Isolated Acetogenins and Biological Activities

Identifiers

InChI

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

0 references

InChIKey

RTATXGUCZHCSNG-ZFDPGQBLSA-N

0 references

2 references

17 September 2022