(2R)-2-[(3,4-dihydroxyphenyl)methyl]-2,6-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1-benzofuran-3-one

Details

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Internal ID d4e7074d-95bc-4b92-a330-1fe25edb2dd7
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Aurone O-glycosides
IUPAC Name (2R)-2-[(3,4-dihydroxyphenyl)methyl]-2,6-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1-benzofuran-3-one
SMILES (Canonical) C1=CC(=C(C=C1CC2(C(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O
SMILES (Isomeric) C1=CC(=C(C=C1C[C@@]2(C(=O)C3=C(O2)C=C(C=C3O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O)O)O)O
InChI InChI=1S/C21H22O12/c22-7-14-16(26)17(27)18(28)20(32-14)31-12-4-9(23)5-13-15(12)19(29)21(30,33-13)6-8-1-2-10(24)11(25)3-8/h1-5,14,16-18,20,22-28,30H,6-7H2/t14-,16-,17+,18-,20-,21-/m1/s1
InChI Key ULGWUUUILLJLSJ-YDKFGTHVSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H22O12
Molecular Weight 466.40 g/mol
Exact Mass 466.11112613 g/mol
Topological Polar Surface Area (TPSA) 207.00 Ų
XlogP -0.50
Atomic LogP (AlogP) -1.51
H-Bond Acceptor 12
H-Bond Donor 8
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R)-2-[(3,4-dihydroxyphenyl)methyl]-2,6-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1-benzofuran-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5084 50.84%
Caco-2 - 0.9315 93.15%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.5808 58.08%
OATP2B1 inhibitior - 0.5562 55.62%
OATP1B1 inhibitior + 0.9150 91.50%
OATP1B3 inhibitior + 0.9339 93.39%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.5501 55.01%
P-glycoprotein inhibitior - 0.6769 67.69%
P-glycoprotein substrate - 0.8480 84.80%
CYP3A4 substrate + 0.6100 61.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8228 82.28%
CYP3A4 inhibition - 0.8508 85.08%
CYP2C9 inhibition - 0.9378 93.78%
CYP2C19 inhibition - 0.8755 87.55%
CYP2D6 inhibition - 0.8767 87.67%
CYP1A2 inhibition - 0.8983 89.83%
CYP2C8 inhibition + 0.5772 57.72%
CYP inhibitory promiscuity - 0.8599 85.99%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5999 59.99%
Eye corrosion - 0.9927 99.27%
Eye irritation - 0.8591 85.91%
Skin irritation - 0.7854 78.54%
Skin corrosion - 0.9565 95.65%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6499 64.99%
Micronuclear + 0.6233 62.33%
Hepatotoxicity - 0.8125 81.25%
skin sensitisation - 0.8493 84.93%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.6562 65.62%
Acute Oral Toxicity (c) III 0.5433 54.33%
Estrogen receptor binding + 0.7575 75.75%
Androgen receptor binding + 0.6320 63.20%
Thyroid receptor binding - 0.4925 49.25%
Glucocorticoid receptor binding + 0.5852 58.52%
Aromatase binding + 0.5492 54.92%
PPAR gamma + 0.6761 67.61%
Honey bee toxicity - 0.6329 63.29%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.7732 77.32%

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 99.64% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.01% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.52% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.19% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.26% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.65% 89.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.33% 96.95%
CHEMBL3194 P02766 Transthyretin 88.33% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.83% 95.56%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 87.64% 80.78%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.38% 95.89%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.86% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.61% 99.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.53% 97.09%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 84.43% 86.92%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.61% 86.33%
CHEMBL4208 P20618 Proteasome component C5 83.39% 90.00%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 83.17% 95.17%
CHEMBL3401 O75469 Pregnane X receptor 82.84% 94.73%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 82.27% 96.21%

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.
Artocarpus tonkinensis

Cross-Links

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PubChem 10050181
LOTUS LTS0096560
wikiData Q105275112