(Q27284825)

UNII-NE54EDY436 (English)

5,7-dihydroxy-2-[4-hydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one

14 October 2016

stereoisomer of

1 reference

based on heuristic

inferred from InChI

5,7-dihydroxy-2-[4-hydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one

1 reference

based on heuristic

inferred from InChI

3'-(alpha-D-Glucopyranosyloxy)-4',5,7-trihydroxyflavone

1 reference

based on heuristic

inferred from InChI

chemical formula

C₂₁H₂₀O₁₁

1 reference

UNII-NE54EDY436 (English)

14 October 2016

canonical SMILES

C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O

1 reference

UNII-NE54EDY436 (English)

14 October 2016

isomeric SMILES

C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O

1 reference

Unusual flavonoids produced by callus of Hypericum perforatum

UNII-NE54EDY436 (English)

14 October 2016

1 reference

Ginkgo biloba

4 references

Identification and determination of the flavonoids from Ginkgo biloba by high-performance liquid chromatography

Complex flavonol glycosides from the leaves of Ginkgo biloba

Biologically active secondary metabolites from myxobacteria

Biologically active secondary metabolites from Ginkgo biloba

Ferula varia

1 reference

Luteolin glucosides from Ferula varia

Meadow vetchling

1 reference

Flavonoid glycosides of Lathyrus pratensisleguminosae

Arnica chamissonis

1 reference

New Flavonoid Glycosides from Arnicae Flos DAB 91

Punica granatum

2 references

Leaf phenolics of Punica granatum

Qualitative Analysis of Polyphenols in Macroporous Resin Pretreated Pomegranate Husk Extract by HPLC-QTOF-MS.

Hypericum erectum

1 reference

Chemical constituents of Hypericum erectum Thunb

Oxytropis campestris

1 reference

Flavonoid studies in four species of the Oxytropis campestris complex (Fabaceae–Galegeae)

Artemisia austriaca

1 reference

Flavonoids ofArtemisia austriaca

Centaurea regia

1 reference

Palmitic acid ester of sitosteryl 3β-glucoside from Centaurea regia

Chrozophora brocchiana

1 reference

Chrozophora rottleri

1 reference

Chrozophora tinctoria

1 reference

Chrozophora verbascifolia

1 reference

Cynara cardunculus

1 reference

The flavonoids of Cynara sibthorpiana

Cynara scolymus

1 reference

The flavonoids of Cynara sibthorpiana

Digitalis ciliata

1 reference

Flavonoids from the leaves ofDigitalis ciliata

Lawsonia inermis

1 reference

New Phenolic Glucosides from Lawsonia inermis

Podocarpus nivalis

1 reference

7-O-methyl-(2R:3R)-dihydroquercetin 5-O-β-D-glucoside and other flavonoids from Podocarpus nivalis

Salvia moorcroftiana

2 references

New Glycosides from Salvia moorcroftiana (Lamiaceae)

Flavonoid glycosides from Salvia moorcroftiana wall.

Trichosanthes kirilowii

1 reference

A chemotaxonomic study of flavonoids in the leaves of six Trichosanthes species

Trifolium trichocephalum

1 reference

Flavonoids fromTrifolium trichocephalum

Helichrysum arenarium

1 reference

Medicinal flowers. XXX. Eight new glycosides, everlastosides F-M, from the flowers of Helichrysum arenarium

Duhaldea cappa

1 reference

Chemical constituents from Inula cappa

Meehania urticifolia

1 reference

New phenolic compounds from Meehania urticifolia

Saussurea hieracioides

1 reference

Chemical constituents of Saussurea superba

Saussurea superba

1 reference

Chemical constituents of Saussurea superba

Hebe parviflora

1 reference

Flavonoid characters contributing to the taxonomic revision of the Hebe parviflora complex

Phyllocladus trichomanoides var. alpinus

1 reference

Uniformity and distinctness of phyllocladus as evidenced by flavonoid accumulation

Chrozophora obliqua

1 reference

Artemisia judaica

1 reference

Flavonoids of Artemisia judaica, A. Monosperma and A. herba-alba

Chrozophora plicata

1 reference

Satureja cuneifolia

1 reference

Free Flavone Aglycones and Flavonoid Glycosides fromSatureia obovata

Identifiers

InChI

InChI=1S/C21H20O11/c22-7-16-18(27)19(28)20(29)21(32-16)31-14-3-8(1-2-10(14)24)13-6-12(26)17-11(25)4-9(23)5-15(17)30-13/h1-6,16,18-25,27-29H,7H2/t16-,18-,19+,20-,21-/m1/s1

1 reference

UNII-NE54EDY436 (English)

14 October 2016

1 reference

Global Substance Registration System

UNII-NE54EDY436 (English)

14 October 2016

1 reference

UNII

NE54EDY436

luteolin 3'-glucoside (English)

14 October 2016

1 reference

5-(5,7-Dihydroxy-4-oxo-4H-chromen-2-yl)-2-hydroxyphenyl beta-D-glucopyranoside (English)

14 October 2016

2 references

UNII-NE54EDY436 (English)

matched by identifier from

14 October 2016

1 reference

DSSTOX compound identifier

CHEMBL1221790 (English)

14 October 2016

1 reference

0 references

0 references

2 references

Global Substance Registration System

UNII

NE54EDY436

luteolin 3'-glucoside (English)

matched by identifier from

14 October 2016

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

1 reference

15 January 2022