o-Cresol

Details

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Internal ID ae611be7-3f39-46cf-9fac-ab2dc807dc93
Taxonomy Benzenoids > Phenols > Cresols > Ortho cresols
IUPAC Name 2-methylphenol
SMILES (Canonical) CC1=CC=CC=C1O
SMILES (Isomeric) CC1=CC=CC=C1O
InChI InChI=1S/C7H8O/c1-6-4-2-3-5-7(6)8/h2-5,8H,1H3
InChI Key QWVGKYWNOKOFNN-UHFFFAOYSA-N
Popularity 11,326 references in papers

Physical and Chemical Properties

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Molecular Formula C7H8O
Molecular Weight 108.14 g/mol
Exact Mass 108.057514874 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.70
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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2-Methylphenol
95-48-7
Orthocresol
2-hydroxytoluene
2-Cresol
Phenol, 2-methyl-
o-methylphenol
o-Cresylic acid
o-Oxytoluene
o-Toluol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of o-Cresol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 + 0.9521 95.21%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.8471 84.71%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9585 95.85%
OATP1B3 inhibitior + 0.9799 97.99%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9380 93.80%
P-glycoprotein inhibitior - 0.9913 99.13%
P-glycoprotein substrate - 0.9888 98.88%
CYP3A4 substrate - 0.7483 74.83%
CYP2C9 substrate - 0.7929 79.29%
CYP2D6 substrate - 0.6905 69.05%
CYP3A4 inhibition - 0.9506 95.06%
CYP2C9 inhibition - 0.9203 92.03%
CYP2C19 inhibition - 0.8627 86.27%
CYP2D6 inhibition - 0.9683 96.83%
CYP1A2 inhibition + 0.6617 66.17%
CYP2C8 inhibition - 0.9015 90.15%
CYP inhibitory promiscuity - 0.7616 76.16%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6329 63.29%
Carcinogenicity (trinary) Non-required 0.6000 60.00%
Eye corrosion + 0.9959 99.59%
Eye irritation + 0.9974 99.74%
Skin irritation + 0.9394 93.94%
Skin corrosion + 0.9795 97.95%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8478 84.78%
Micronuclear - 0.7652 76.52%
Hepatotoxicity + 0.8500 85.00%
skin sensitisation + 0.9769 97.69%
Respiratory toxicity - 0.9889 98.89%
Reproductive toxicity + 0.7503 75.03%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.5542 55.42%
Acute Oral Toxicity (c) II 0.7686 76.86%
Estrogen receptor binding - 0.9168 91.68%
Androgen receptor binding - 0.7917 79.17%
Thyroid receptor binding - 0.8430 84.30%
Glucocorticoid receptor binding - 0.9004 90.04%
Aromatase binding - 0.9016 90.16%
PPAR gamma - 0.8611 86.11%
Honey bee toxicity - 0.9928 99.28%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.8418 84.18%

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 91.04% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.03% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.16% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 85.61% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.41% 93.65%

Cross-Links

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PubChem 335
NPASS NPC286904
LOTUS LTS0108586
wikiData Q312708