2-(2-Methoxyphenoxy)phenol

Details

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Internal ID 6d4721a2-66d8-4341-bef3-c666fb5e9b22
Taxonomy Benzenoids > Benzene and substituted derivatives > Diphenylethers
IUPAC Name 2-(2-methoxyphenoxy)phenol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H12O3/c1-15-12-8-4-5-9-13(12)16-11-7-3-2-6-10(11)14/h2-9,14H,1H3
InChI Key OHMCFTVLHBWELH-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C13H12O3
Molecular Weight 216.23 g/mol
Exact Mass 216.078644241 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.19
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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Phenol, o-(o-methoxyphenoxy)-
21905-60-2
o-(o-Methoxyphenoxy)phenol
SCHEMBL6830290
DTXSID50341399
OHMCFTVLHBWELH-UHFFFAOYSA-N
2-Hydroxy-2'-methoxy diphenyl ether

2D Structure

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2D Structure of 2-(2-Methoxyphenoxy)phenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.8460 84.60%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Mitochondria 0.9022 90.22%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9602 96.02%
OATP1B3 inhibitior + 0.9758 97.58%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7142 71.42%
P-glycoprotein inhibitior - 0.9633 96.33%
P-glycoprotein substrate - 0.9626 96.26%
CYP3A4 substrate - 0.6491 64.91%
CYP2C9 substrate - 0.7864 78.64%
CYP2D6 substrate + 0.3813 38.13%
CYP3A4 inhibition - 0.9124 91.24%
CYP2C9 inhibition - 0.8123 81.23%
CYP2C19 inhibition + 0.7508 75.08%
CYP2D6 inhibition - 0.9371 93.71%
CYP1A2 inhibition + 0.7120 71.20%
CYP2C8 inhibition - 0.7033 70.33%
CYP inhibitory promiscuity + 0.5594 55.94%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7360 73.60%
Carcinogenicity (trinary) Warning 0.4675 46.75%
Eye corrosion - 0.8495 84.95%
Eye irritation + 0.9428 94.28%
Skin irritation + 0.5782 57.82%
Skin corrosion - 0.9492 94.92%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6627 66.27%
Micronuclear - 0.6018 60.18%
Hepatotoxicity + 0.5659 56.59%
skin sensitisation - 0.6805 68.05%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.6478 64.78%
Acute Oral Toxicity (c) III 0.7055 70.55%
Estrogen receptor binding + 0.7234 72.34%
Androgen receptor binding - 0.8378 83.78%
Thyroid receptor binding + 0.5321 53.21%
Glucocorticoid receptor binding + 0.6075 60.75%
Aromatase binding + 0.7922 79.22%
PPAR gamma + 0.6303 63.03%
Honey bee toxicity - 0.9617 96.17%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9204 92.04%

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 94.94% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.77% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.54% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.82% 86.33%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 85.33% 89.62%
CHEMBL2535 P11166 Glucose transporter 84.58% 98.75%
CHEMBL1255126 O15151 Protein Mdm4 83.09% 90.20%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 80.38% 91.79%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.36% 94.00%

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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There are no matching plants.

Cross-Links

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PubChem 572803
NPASS NPC161339