[3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate

Details

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Internal ID 58968f30-636e-48fc-8854-a1d43df41ddd
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-7-O-glycosides
IUPAC Name [3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate
SMILES (Canonical) C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O
SMILES (Isomeric) C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O
InChI InChI=1S/C30H26O12/c31-17-6-1-15(2-7-17)3-10-25(35)39-14-24-27(36)28(37)29(38)30(42-24)40-19-11-20(33)26-21(34)13-22(41-23(26)12-19)16-4-8-18(32)9-5-16/h1-13,24,27-33,36-38H,14H2
InChI Key WPQRDUGBKUNFJW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H26O12
Molecular Weight 578.50 g/mol
Exact Mass 578.14242626 g/mol
Topological Polar Surface Area (TPSA) 192.00 Ų
XlogP 2.60

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate

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 99.42% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 97.94% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 97.72% 89.00%
CHEMBL3194 P02766 Transthyretin 97.24% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.92% 86.33%
CHEMBL2581 P07339 Cathepsin D 92.05% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.12% 97.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.69% 99.15%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 89.00% 91.71%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 88.46% 95.78%
CHEMBL3401 O75469 Pregnane X receptor 88.11% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.81% 94.45%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 87.11% 95.64%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.74% 90.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.67% 96.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 86.47% 86.92%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.22% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.98% 99.17%
CHEMBL242 Q92731 Estrogen receptor beta 85.70% 98.35%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.39% 95.56%
CHEMBL3922 P50579 Methionine aminopeptidase 2 82.78% 97.28%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.57% 95.89%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 81.54% 83.57%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.79% 95.50%
CHEMBL2179 P04062 Beta-glucocerebrosidase 80.59% 85.31%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.43% 95.89%

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.
Dasiphora fruticosa
Leucas aspera
Leucas cephalotes
Leucas neufliseana
Marrubium vulgare
Phlomis aurea
Populus tremuloides
Scolopia chinensis
Sideritis syriaca
Stachys aegyptiaca
Stachys bombycina
Stachys byzantina
Stachys ocymastrum
Turnera diffusa

Cross-Links

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PubChem 162916367
LOTUS LTS0215870
wikiData Q105310150