(Q27145859)

inferred from SMILES

mass

418.089997±0 dalton

1 reference

Kaempferol 3-xylopyranoside (English)

Kaempferol 3-alpha-D-arabinopyranoside

8 October 2016

stereoisomer of

2 references

inferred from InChIKey

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one

1 reference

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one

inferred from InChIKey

2 references

inferred from InChIKey

4',5,7-Trihydroxy-3-(alpha-D-arabinopyranosyloxy)flavone

1 reference

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}chromen-4-one

1 reference

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one

1 reference

chemical formula

C₂₀H₁₈O₁₀

1 reference

Kaempferol 3-xylopyranoside (English)

8 October 2016

canonical SMILES

C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O

1 reference

Kaempferol 3-xylopyranoside (English)

8 October 2016

isomeric SMILES

C1[C@H]([C@@H]([C@H]([C@@H](O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O

1 reference

Alkaloids and Flavonoids from Ricinus communis

Kaempferol 3-xylopyranoside (English)

8 October 2016

1 reference

Bursera graveolens

1 reference

New Luteolin 3’-O-Acylated Rhamnosides from Leaves of Bursera graveolens

Phoebe formosana

2 references

Polar Chemical Constituents fromPhoebe formosana

Polar Chemical Constituents fromPhoebe formosana

Rubus ulmifolius

1 reference

In vitro antimicrobial activity of extracts and isolated constituents of Rubus ulmifolius

Securidaca diversifolia

1 reference

Flavonol glycosides from Securidaca diversifolia

Tetradium glabrifolium

2 references

Constituents of Leaves of Tetradium Glabrifolium

Constituents of Leaves of Tetradium Glabrifolium

Cinnamomum philippinense

1 reference

Flavonoid Glycosides from the Leaves of Machilus philippinensis

Rosa × damascena

1 reference

Recovery of polyphenols from rose oil distillation wastewater using adsorption resins--a pilot study

Rosa gallica

1 reference

Recovery of polyphenols from rose oil distillation wastewater using adsorption resins--a pilot study

Identifiers

InChI

InChI=1S/C20H18O10/c21-9-3-1-8(2-4-9)18-19(30-20-17(27)15(25)12(24)7-28-20)16(26)14-11(23)5-10(22)6-13(14)29-18/h1-6,12,15,17,20-25,27H,7H2/t12-,15+,17-,20+/m1/s1

1 reference

Kaempferol 3-xylopyranoside (English)

RNVUDWOQYYWXBJ-BWYUNELBSA-N

8 October 2016

InChIKey

2 references

Kaempferol 3-xylopyranoside (English)

8 October 2016

ChEBI release 2020-09-01

1 reference

Kaempferol-3-O-alpha-L-arabinoside (English)

8 October 2016

2 references

Kaempferol 3-xylopyranoside (English)

matched by identifier from

8 October 2016

InChIKey

RNVUDWOQYYWXBJ-BWYUNELBSA-N

Reaxys registry number

7575960

1 reference

kaempferol 3-O-beta-D-xyloside (English)

8 October 2016

ChEBI ID

76294

mapping relation type

2 references

kaempferol 3-O-beta-D-xyloside (English)