(Q105371326)

inferred from SMILES

mass

432.10564684 dalton

1 reference

2 references

inferred from InChIKey

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

1 reference

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

1 reference

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

1 reference

chemical formula

C₂₁H₂₀O₁₀

0 references

canonical SMILES

O=C1C(=COC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC(O)=C12)C=4C=CC(O)=CC4

0 references

isomeric SMILES

O=c1c(-c2ccc(O)cc2)coc2cc(O[C@@H]3O[C@@H](CO)[C@@H](O)[C@H](O)[C@H]3O)cc(O)c12

0 references

found in taxon

Baptisia bracteata

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia cinerea

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia lanceolata

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia lecontei

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia megacarpa

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia nuttalliana

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Ficus septica

1 reference

Ficus spp. (fig): ethnobotany and potential as anticancer and anti-inflammatory agents

Genista ephedroides

1 reference

Flavonoids from Genista ephedroides

Lupinus albus

1 reference

New Isoflavone Glucosides from White Lupin (Lupinus albus L.)

Retama sphaerocarpa

1 reference

An isoflavone glucoside from Retama sphaerocarpa boissier

Styphnolobium japonicum

1 reference

Four new isoflavone triglycosides from Sophora japonica

Thermopsis lanceolata

1 reference

Flavonoids of Thermopsis alterniflora

Thermopsis macrophylla

1 reference

Thermopsis mollis

1 reference

Thermopsis rhombifolia

1 reference

Thermopsis villosa

1 reference

Trifolium pratense

1 reference

LC-ESI-MS study of the flavonoid glycoside malonates of red clover (Trifolium pratense)

radish

1 reference

Deciphering the Nutraceutical Potential of -A Comprehensive Overview

Phaseolus vulgaris

1 reference

Biotransformation of common bean (Phaseolus vulgaris L.) flavonoid glycosides by bifidobacterium species from human intestinal origin

Cymbopogon citratus

1 reference

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

Capsicum annuum

1 reference

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

Chamaecytisus eriocarpus

1 reference