4,4'-Dihydroxy-3,3',5,alpha-tetramethoxybibenzyl

Details

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Internal ID 89e2684a-fabe-4268-8790-9d379c8b51ca
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 4-[2-(4-hydroxy-3-methoxyphenyl)-1-methoxyethyl]-2,6-dimethoxyphenol
SMILES (Canonical) COC1=CC(=CC(=C1O)OC)C(CC2=CC(=C(C=C2)O)OC)OC
SMILES (Isomeric) COC1=CC(=CC(=C1O)OC)C(CC2=CC(=C(C=C2)O)OC)OC
InChI InChI=1S/C18H22O6/c1-21-14(7-11-5-6-13(19)15(8-11)22-2)12-9-16(23-3)18(20)17(10-12)24-4/h5-6,8-10,14,19-20H,7H2,1-4H3
InChI Key KMEWJFKKURMVAV-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C18H22O6
Molecular Weight 334.40 g/mol
Exact Mass 334.14163842 g/mol
Topological Polar Surface Area (TPSA) 77.40 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.05
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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4,4'-dihydroxy-3,3',5,alpha-tetramethoxybibenzyl

2D Structure

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2D Structure of 4,4'-Dihydroxy-3,3',5,alpha-tetramethoxybibenzyl

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9849 98.49%
Caco-2 + 0.8098 80.98%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8206 82.06%
OATP2B1 inhibitior - 0.8566 85.66%
OATP1B1 inhibitior + 0.8465 84.65%
OATP1B3 inhibitior + 0.8634 86.34%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5654 56.54%
P-glycoprotein inhibitior - 0.7792 77.92%
P-glycoprotein substrate - 0.7911 79.11%
CYP3A4 substrate - 0.5679 56.79%
CYP2C9 substrate - 0.6092 60.92%
CYP2D6 substrate + 0.4755 47.55%
CYP3A4 inhibition - 0.8347 83.47%
CYP2C9 inhibition - 0.8397 83.97%
CYP2C19 inhibition + 0.7609 76.09%
CYP2D6 inhibition - 0.5762 57.62%
CYP1A2 inhibition + 0.6363 63.63%
CYP2C8 inhibition + 0.6323 63.23%
CYP inhibitory promiscuity + 0.5688 56.88%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7850 78.50%
Carcinogenicity (trinary) Non-required 0.6751 67.51%
Eye corrosion - 0.9797 97.97%
Eye irritation - 0.5969 59.69%
Skin irritation - 0.8204 82.04%
Skin corrosion - 0.9591 95.91%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6497 64.97%
Micronuclear - 0.5582 55.82%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.8298 82.98%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity - 0.8470 84.70%
Acute Oral Toxicity (c) III 0.7272 72.72%
Estrogen receptor binding + 0.7067 70.67%
Androgen receptor binding - 0.5761 57.61%
Thyroid receptor binding + 0.8038 80.38%
Glucocorticoid receptor binding + 0.7577 75.77%
Aromatase binding - 0.5549 55.49%
PPAR gamma + 0.5637 56.37%
Honey bee toxicity - 0.8893 88.93%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6451 64.51%
Fish aquatic toxicity + 0.9452 94.52%

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 96.22% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.39% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.28% 98.95%
CHEMBL1255126 O15151 Protein Mdm4 92.72% 90.20%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 91.59% 95.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.54% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.24% 94.45%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.09% 99.15%
CHEMBL3492 P49721 Proteasome Macropain subunit 86.98% 90.24%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.03% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.06% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.81% 92.62%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 82.62% 92.68%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.52% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 82.28% 94.73%
CHEMBL2535 P11166 Glucose transporter 82.27% 98.75%
CHEMBL4208 P20618 Proteasome component C5 81.88% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.48% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.45% 85.14%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.38% 96.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 80.33% 89.62%

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.
Dendrobium loddigesii

Cross-Links

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PubChem 75149948
LOTUS LTS0186282
wikiData Q105142952