Methyl 6-(5,6-dihydroxy-4-oxo-2-phenylchromen-7-yl)oxy-3,4,5-trihydroxyoxane-2-carboxylate

Details

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Internal ID c6b242fe-c26e-41a1-a50a-b32fe09815b5
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glucuronides > Flavonoid-7-O-glucuronides
IUPAC Name methyl 6-(5,6-dihydroxy-4-oxo-2-phenylchromen-7-yl)oxy-3,4,5-trihydroxyoxane-2-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H20O11/c1-30-21(29)20-18(27)17(26)19(28)22(33-20)32-13-8-12-14(16(25)15(13)24)10(23)7-11(31-12)9-5-3-2-4-6-9/h2-8,17-20,22,24-28H,1H3
InChI Key AOWRAYJMTOYETH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H20O11
Molecular Weight 460.40 g/mol
Exact Mass 460.10056145 g/mol
Topological Polar Surface Area (TPSA) 172.00 Ų
XlogP 1.40
Atomic LogP (AlogP) 0.23
H-Bond Acceptor 11
H-Bond Donor 5
Rotatable Bonds 4

Synonyms

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SCHEMBL17663707
HDA47503

2D Structure

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2D Structure of Methyl 6-(5,6-dihydroxy-4-oxo-2-phenylchromen-7-yl)oxy-3,4,5-trihydroxyoxane-2-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7483 74.83%
Caco-2 - 0.9159 91.59%
Blood Brain Barrier - 0.8750 87.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6619 66.19%
OATP2B1 inhibitior + 0.6314 63.14%
OATP1B1 inhibitior + 0.8774 87.74%
OATP1B3 inhibitior + 0.9857 98.57%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7340 73.40%
P-glycoprotein inhibitior - 0.6147 61.47%
P-glycoprotein substrate - 0.7470 74.70%
CYP3A4 substrate + 0.6212 62.12%
CYP2C9 substrate - 0.6438 64.38%
CYP2D6 substrate - 0.8738 87.38%
CYP3A4 inhibition - 0.7674 76.74%
CYP2C9 inhibition - 0.8642 86.42%
CYP2C19 inhibition - 0.8511 85.11%
CYP2D6 inhibition - 0.9471 94.71%
CYP1A2 inhibition - 0.6411 64.11%
CYP2C8 inhibition + 0.7891 78.91%
CYP inhibitory promiscuity - 0.7677 76.77%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5903 59.03%
Eye corrosion - 0.9867 98.67%
Eye irritation - 0.8857 88.57%
Skin irritation - 0.6835 68.35%
Skin corrosion - 0.9231 92.31%
Ames mutagenesis - 0.5464 54.64%
Human Ether-a-go-go-Related Gene inhibition - 0.5843 58.43%
Micronuclear + 0.9000 90.00%
Hepatotoxicity - 0.7375 73.75%
skin sensitisation - 0.9291 92.91%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.7586 75.86%
Acute Oral Toxicity (c) III 0.5786 57.86%
Estrogen receptor binding + 0.8364 83.64%
Androgen receptor binding + 0.7699 76.99%
Thyroid receptor binding + 0.5527 55.27%
Glucocorticoid receptor binding + 0.6934 69.34%
Aromatase binding + 0.5374 53.74%
PPAR gamma + 0.7122 71.22%
Honey bee toxicity - 0.7198 71.98%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5749 57.49%
Fish aquatic toxicity + 0.9235 92.35%

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 99.17% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.03% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.87% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.16% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.12% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.81% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.49% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.74% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.69% 99.17%
CHEMBL5284 Q96RR4 CaM-kinase kinase beta 87.49% 89.23%
CHEMBL3401 O75469 Pregnane X receptor 86.71% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.70% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.16% 99.23%
CHEMBL1951 P21397 Monoamine oxidase A 80.33% 91.49%

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.
Scutellaria baicalensis

Cross-Links

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PubChem 72747690
LOTUS LTS0063942
wikiData Q104916012