4-Hydroxy-3'-methoxybibenzyl

Details

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Internal ID fd3efc45-65fb-4ab8-b217-b574a974d53b
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 4-[2-(3-methoxyphenyl)ethyl]phenol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H16O2/c1-17-15-4-2-3-13(11-15)6-5-12-7-9-14(16)10-8-12/h2-4,7-11,16H,5-6H2,1H3
InChI Key QHWSNPUNTSCHIE-UHFFFAOYSA-N
Popularity 21 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O2
Molecular Weight 228.29 g/mol
Exact Mass 228.115029749 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.19
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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59586-27-5
4-(2-(3-Methoxyphenyl)ethyl)phenol
3-methoxy-4'-hydroxybibenzyl
CHEMBL478934
DTXSID40208245
Phenol, 4-(2-(3-methoxyphenyl)ethyl)-

2D Structure

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2D Structure of 4-Hydroxy-3'-methoxybibenzyl

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9962 99.62%
Caco-2 + 0.8485 84.85%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.8784 87.84%
OATP2B1 inhibitior - 0.8547 85.47%
OATP1B1 inhibitior + 0.8808 88.08%
OATP1B3 inhibitior + 0.9417 94.17%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.6327 63.27%
P-glycoprotein inhibitior - 0.9384 93.84%
P-glycoprotein substrate + 0.5929 59.29%
CYP3A4 substrate - 0.5349 53.49%
CYP2C9 substrate - 0.6120 61.20%
CYP2D6 substrate + 0.5079 50.79%
CYP3A4 inhibition - 0.8825 88.25%
CYP2C9 inhibition - 0.7852 78.52%
CYP2C19 inhibition + 0.8409 84.09%
CYP2D6 inhibition - 0.9114 91.14%
CYP1A2 inhibition + 0.8584 85.84%
CYP2C8 inhibition + 0.8271 82.71%
CYP inhibitory promiscuity + 0.5531 55.31%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6442 64.42%
Carcinogenicity (trinary) Non-required 0.5204 52.04%
Eye corrosion - 0.9124 91.24%
Eye irritation + 0.9512 95.12%
Skin irritation - 0.7035 70.35%
Skin corrosion - 0.9455 94.55%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6340 63.40%
Micronuclear - 0.8000 80.00%
Hepatotoxicity - 0.7625 76.25%
skin sensitisation - 0.5675 56.75%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity - 0.7501 75.01%
Acute Oral Toxicity (c) III 0.7974 79.74%
Estrogen receptor binding + 0.8278 82.78%
Androgen receptor binding + 0.8344 83.44%
Thyroid receptor binding + 0.5897 58.97%
Glucocorticoid receptor binding - 0.4905 49.05%
Aromatase binding + 0.5675 56.75%
PPAR gamma + 0.6700 67.00%
Honey bee toxicity - 0.8576 85.76%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.6766 67.66%

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
CHEMBL2581 P07339 Cathepsin D 96.31% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.16% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.43% 91.11%
CHEMBL2535 P11166 Glucose transporter 91.84% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.69% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.36% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.81% 95.56%
CHEMBL226 P30542 Adenosine A1 receptor 88.25% 95.93%
CHEMBL3401 O75469 Pregnane X receptor 88.07% 94.73%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 87.98% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.38% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.89% 94.45%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 86.74% 86.92%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.58% 96.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.53% 95.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.16% 95.89%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.85% 93.99%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 83.71% 96.09%
CHEMBL5203 P33316 dUTP pyrophosphatase 82.75% 99.18%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.68% 91.71%
CHEMBL3231 Q13464 Rho-associated protein kinase 1 82.64% 95.55%
CHEMBL1907 P15144 Aminopeptidase N 82.53% 93.31%
CHEMBL4208 P20618 Proteasome component C5 82.09% 90.00%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 81.61% 92.67%

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.
Frullania davurica
Plagiochila heteromalla

Cross-Links

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PubChem 173687
LOTUS LTS0045061
wikiData Q83082351