(2S)-7-(3,4-dimethoxyphenyl)-4,6-dihydroxy-2-prop-1-en-2-yl-2,3-dihydrofuro[3,2-g]chromen-5-one

Details

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Internal ID f121b756-8f4a-4f88-94f8-8c348c20ab97
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavones > 6-prenylated flavones
IUPAC Name (2S)-7-(3,4-dimethoxyphenyl)-4,6-dihydroxy-2-prop-1-en-2-yl-2,3-dihydrofuro[3,2-g]chromen-5-one
SMILES (Canonical) CC(=C)C1CC2=C(O1)C=C3C(=C2O)C(=O)C(=C(O3)C4=CC(=C(C=C4)OC)OC)O
SMILES (Isomeric) CC(=C)[C@@H]1CC2=C(O1)C=C3C(=C2O)C(=O)C(=C(O3)C4=CC(=C(C=C4)OC)OC)O
InChI InChI=1S/C22H20O7/c1-10(2)14-8-12-15(28-14)9-17-18(19(12)23)20(24)21(25)22(29-17)11-5-6-13(26-3)16(7-11)27-4/h5-7,9,14,23,25H,1,8H2,2-4H3/t14-/m0/s1
InChI Key HHIZPGUSWOTUAE-AWEZNQCLSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C22H20O7
Molecular Weight 396.40 g/mol
Exact Mass 396.12090297 g/mol
Topological Polar Surface Area (TPSA) 94.40 Ų
XlogP 4.50
Atomic LogP (AlogP) 3.77
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S)-7-(3,4-dimethoxyphenyl)-4,6-dihydroxy-2-prop-1-en-2-yl-2,3-dihydrofuro[3,2-g]chromen-5-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9934 99.34%
Caco-2 - 0.6284 62.84%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7053 70.53%
OATP2B1 inhibitior - 0.7131 71.31%
OATP1B1 inhibitior + 0.9193 91.93%
OATP1B3 inhibitior + 0.8932 89.32%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5630 56.30%
P-glycoprotein inhibitior + 0.8032 80.32%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.6332 63.32%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition + 0.5471 54.71%
CYP2C9 inhibition + 0.5207 52.07%
CYP2C19 inhibition + 0.8425 84.25%
CYP2D6 inhibition - 0.8564 85.64%
CYP1A2 inhibition + 0.5466 54.66%
CYP2C8 inhibition + 0.7762 77.62%
CYP inhibitory promiscuity + 0.7895 78.95%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5601 56.01%
Eye corrosion - 0.9882 98.82%
Eye irritation - 0.6874 68.74%
Skin irritation - 0.7556 75.56%
Skin corrosion - 0.9448 94.48%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6536 65.36%
Micronuclear + 0.6459 64.59%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.7764 77.64%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.8648 86.48%
Acute Oral Toxicity (c) II 0.4884 48.84%
Estrogen receptor binding + 0.8732 87.32%
Androgen receptor binding + 0.6469 64.69%
Thyroid receptor binding + 0.7134 71.34%
Glucocorticoid receptor binding + 0.8583 85.83%
Aromatase binding + 0.7394 73.94%
PPAR gamma + 0.8175 81.75%
Honey bee toxicity - 0.5956 59.56%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9862 98.62%

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 96.95% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.19% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.14% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.65% 94.00%
CHEMBL2581 P07339 Cathepsin D 94.44% 98.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 93.81% 92.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.68% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.26% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.93% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 91.50% 91.49%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 90.25% 83.10%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.57% 95.89%
CHEMBL3438 Q05513 Protein kinase C zeta 88.47% 88.48%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.21% 95.56%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 87.16% 95.78%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.73% 99.23%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.75% 90.71%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 82.52% 95.53%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.07% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 81.97% 94.73%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.80% 97.14%
CHEMBL217 P14416 Dopamine D2 receptor 80.71% 95.62%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.02% 100.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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Cross-Links

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PubChem 162901394
LOTUS LTS0031270
wikiData Q105028312