Guaiacol

Details

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Internal ID e9572d81-136b-476f-b9fa-b94029b1b6e1
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 2-methoxyphenol
SMILES (Canonical) COC1=CC=CC=C1O
SMILES (Isomeric) COC1=CC=CC=C1O
InChI InChI=1S/C7H8O2/c1-9-7-5-3-2-4-6(7)8/h2-5,8H,1H3
InChI Key LHGVFZTZFXWLCP-UHFFFAOYSA-N
Popularity 12,816 references in papers

Physical and Chemical Properties

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Molecular Formula C7H8O2
Molecular Weight 124.14 g/mol
Exact Mass 124.052429494 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.40
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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2-Methoxyphenol
90-05-1
o-Methoxyphenol
2-Hydroxyanisole
Guaiastil
Pyroguaiac acid
o-Guaiacol
o-Hydroxyanisole
Pyrocatechol monomethyl ether
Phenol, 2-methoxy-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Guaiacol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9953 99.53%
Caco-2 + 0.9344 93.44%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.8751 87.51%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9611 96.11%
OATP1B3 inhibitior + 0.9829 98.29%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9520 95.20%
P-glycoprotein inhibitior - 0.9904 99.04%
P-glycoprotein substrate - 0.9788 97.88%
CYP3A4 substrate - 0.7060 70.60%
CYP2C9 substrate - 0.7845 78.45%
CYP2D6 substrate + 0.4222 42.22%
CYP3A4 inhibition - 0.9673 96.73%
CYP2C9 inhibition - 0.9701 97.01%
CYP2C19 inhibition - 0.7926 79.26%
CYP2D6 inhibition - 0.9543 95.43%
CYP1A2 inhibition - 0.7206 72.06%
CYP2C8 inhibition - 0.7463 74.63%
CYP inhibitory promiscuity - 0.7984 79.84%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7178 71.78%
Carcinogenicity (trinary) Warning 0.5195 51.95%
Eye corrosion + 0.9051 90.51%
Eye irritation + 0.9973 99.73%
Skin irritation + 0.9120 91.20%
Skin corrosion + 0.5595 55.95%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7249 72.49%
Micronuclear - 0.7737 77.37%
Hepatotoxicity - 0.5178 51.78%
skin sensitisation + 0.9126 91.26%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.5689 56.89%
Acute Oral Toxicity (c) III 0.8390 83.90%
Estrogen receptor binding - 0.7873 78.73%
Androgen receptor binding - 0.8862 88.62%
Thyroid receptor binding - 0.8584 85.84%
Glucocorticoid receptor binding - 0.9259 92.59%
Aromatase binding - 0.8794 87.94%
PPAR gamma - 0.8742 87.42%
Honey bee toxicity - 0.9713 97.13%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity - 0.4238 42.38%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL205 P00918 Carbonic anhydrase II 2940 nM
Ki
PMID: 19231207
CHEMBL4096 P04637 Cellular tumor antigen p53 12.6 nM
12.6 nM
Potency
Potency
via CMAUP
via Super-PRED
CHEMBL1963 P16473 Thyroid stimulating hormone receptor 5011.9 nM
5011.9 nM
Potency
Potency
via CMAUP
via CMAUP

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.38% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.09% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.23% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.38% 86.33%
CHEMBL2535 P11166 Glucose transporter 85.07% 98.75%
CHEMBL1255126 O15151 Protein Mdm4 83.56% 90.20%
CHEMBL2581 P07339 Cathepsin D 81.69% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.80% 94.00%

Cross-Links

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PubChem 460
NPASS NPC114325
ChEMBL CHEMBL13766
LOTUS LTS0179228
wikiData Q412403