4,4'-(Ethane-1,2-diyl)bis(2,3,6-trimethoxyphenol)

Details

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Internal ID 57a3fda7-663d-4d64-8ace-1523718d586b
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 4-[2-(4-hydroxy-2,3,5-trimethoxyphenyl)ethyl]-2,3,6-trimethoxyphenol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H26O8/c1-23-13-9-11(17(25-3)19(27-5)15(13)21)7-8-12-10-14(24-2)16(22)20(28-6)18(12)26-4/h9-10,21-22H,7-8H2,1-6H3
InChI Key ULIOCVSRDTXGQE-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H26O8
Molecular Weight 394.40 g/mol
Exact Mass 394.16276778 g/mol
Topological Polar Surface Area (TPSA) 95.80 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.93
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,4'-(Ethane-1,2-diyl)bis(2,3,6-trimethoxyphenol)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9616 96.16%
Caco-2 + 0.8468 84.68%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.8675 86.75%
OATP2B1 inhibitior - 0.8630 86.30%
OATP1B1 inhibitior + 0.8609 86.09%
OATP1B3 inhibitior + 0.8644 86.44%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.5960 59.60%
P-glycoprotein inhibitior - 0.7553 75.53%
P-glycoprotein substrate - 0.8875 88.75%
CYP3A4 substrate - 0.6189 61.89%
CYP2C9 substrate - 0.6120 61.20%
CYP2D6 substrate + 0.5079 50.79%
CYP3A4 inhibition - 0.8830 88.30%
CYP2C9 inhibition - 0.6634 66.34%
CYP2C19 inhibition + 0.6923 69.23%
CYP2D6 inhibition - 0.8401 84.01%
CYP1A2 inhibition + 0.5690 56.90%
CYP2C8 inhibition + 0.4740 47.40%
CYP inhibitory promiscuity + 0.6686 66.86%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7043 70.43%
Carcinogenicity (trinary) Non-required 0.6531 65.31%
Eye corrosion - 0.9681 96.81%
Eye irritation + 0.7275 72.75%
Skin irritation - 0.8061 80.61%
Skin corrosion - 0.9346 93.46%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3750 37.50%
Micronuclear - 0.6941 69.41%
Hepatotoxicity - 0.5716 57.16%
skin sensitisation - 0.8210 82.10%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity - 0.8325 83.25%
Acute Oral Toxicity (c) III 0.7629 76.29%
Estrogen receptor binding + 0.8103 81.03%
Androgen receptor binding - 0.5554 55.54%
Thyroid receptor binding + 0.7664 76.64%
Glucocorticoid receptor binding + 0.8056 80.56%
Aromatase binding + 0.7102 71.02%
PPAR gamma + 0.5797 57.97%
Honey bee toxicity - 0.9375 93.75%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5049 50.49%
Fish aquatic toxicity + 0.9168 91.68%

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 97.58% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.27% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.74% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.84% 99.17%
CHEMBL4208 P20618 Proteasome component C5 84.58% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.07% 94.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 83.96% 89.62%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.75% 92.62%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.51% 96.00%
CHEMBL2581 P07339 Cathepsin D 82.43% 98.95%

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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There are no matching plants.

Cross-Links

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PubChem 139584882
LOTUS LTS0138062
wikiData Q77377449