Myricetin-3-O-xyloside

Details

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Internal ID 1a80b007-5dba-4c6a-9c49-82e91c165d7d
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-3-O-glycosides
IUPAC Name 5,7-dihydroxy-3-(3,4,5-trihydroxyoxan-2-yl)oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one
SMILES (Canonical) C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O
SMILES (Isomeric) C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O
InChI InChI=1S/C20H18O12/c21-7-3-8(22)13-12(4-7)31-18(6-1-9(23)14(26)10(24)2-6)19(16(13)28)32-20-17(29)15(27)11(25)5-30-20/h1-4,11,15,17,20-27,29H,5H2
InChI Key SBEOEJNITMVWLK-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C20H18O12
Molecular Weight 450.30 g/mol
Exact Mass 450.07982601 g/mol
Topological Polar Surface Area (TPSA) 207.00 Ų
XlogP 0.10

Synonyms

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CHEBI:192520
Hexahydroxy-flavone (myricetin) pentoside
5,7-dihydroxy-3-(3,4,5-trihydroxyoxan-2-yl)oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one

2D Structure

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2D Structure of Myricetin-3-O-xyloside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
No predicted properties yet!

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.76% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 97.09% 89.00%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 94.67% 95.64%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.33% 94.00%
CHEMBL1951 P21397 Monoamine oxidase A 92.09% 91.49%
CHEMBL2581 P07339 Cathepsin D 89.61% 98.95%
CHEMBL3194 P02766 Transthyretin 89.25% 90.71%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 88.50% 90.71%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.18% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.37% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.19% 97.09%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 85.01% 80.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.02% 99.23%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.04% 92.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.03% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.48% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.04% 86.33%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 81.80% 95.78%
CHEMBL3401 O75469 Pregnane X receptor 81.66% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Epilobium hirsutum
Eucalyptus camaldulensis subsp. camaldulensis
Limonium aureum
Limonium gmelinii
Limonium sinense
Myrsine africana
Saxifraga tricuspidata
Vaccinium macrocarpon

Cross-Links

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PubChem 21477996
LOTUS LTS0072077
wikiData Q105249363