o-Tolyl acetate

Details

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Internal ID 37d28178-49e0-46f2-a044-5fbc6a6549e2
Taxonomy Benzenoids > Phenol esters
IUPAC Name (2-methylphenyl) acetate
SMILES (Canonical) CC1=CC=CC=C1OC(=O)C
SMILES (Isomeric) CC1=CC=CC=C1OC(=O)C
InChI InChI=1S/C9H10O2/c1-7-5-3-4-6-9(7)11-8(2)10/h3-6H,1-2H3
InChI Key AMZORBZSQRUXNC-UHFFFAOYSA-N
Popularity 32 references in papers

Physical and Chemical Properties

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Molecular Formula C9H10O2
Molecular Weight 150.17 g/mol
Exact Mass 150.068079557 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.92
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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533-18-6
o-Cresyl acetate
2-Methylphenyl acetate
o-Cresol acetate
Acetyl-o-cresol
(2-methylphenyl) acetate
2-Acetoxytoluene
ACETIC ACID, 2-METHYLPHENYL ESTER
Tolyl acetate
Acetic acid, o-tolyl ester
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-Tolyl acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8308 83.08%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.9279 92.79%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9787 97.87%
OATP1B3 inhibitior + 0.9850 98.50%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8314 83.14%
P-glycoprotein inhibitior - 0.9854 98.54%
P-glycoprotein substrate - 0.9808 98.08%
CYP3A4 substrate - 0.6363 63.63%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.8564 85.64%
CYP3A4 inhibition - 0.9662 96.62%
CYP2C9 inhibition - 0.9313 93.13%
CYP2C19 inhibition - 0.7161 71.61%
CYP2D6 inhibition - 0.9677 96.77%
CYP1A2 inhibition + 0.7099 70.99%
CYP2C8 inhibition - 0.8722 87.22%
CYP inhibitory promiscuity - 0.7426 74.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6601 66.01%
Carcinogenicity (trinary) Non-required 0.5956 59.56%
Eye corrosion + 0.9379 93.79%
Eye irritation + 0.9956 99.56%
Skin irritation + 0.7548 75.48%
Skin corrosion - 0.9128 91.28%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5882 58.82%
Micronuclear - 0.7493 74.93%
Hepatotoxicity + 0.7784 77.84%
skin sensitisation + 0.7486 74.86%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.6786 67.86%
Acute Oral Toxicity (c) III 0.9140 91.40%
Estrogen receptor binding - 0.9182 91.82%
Androgen receptor binding - 0.9008 90.08%
Thyroid receptor binding - 0.9197 91.97%
Glucocorticoid receptor binding - 0.9325 93.25%
Aromatase binding - 0.8600 86.00%
PPAR gamma - 0.8722 87.22%
Honey bee toxicity - 0.9022 90.22%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9565 95.65%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.47% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.42% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.09% 86.33%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 84.86% 93.65%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.36% 95.50%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.85% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.48% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 80.27% 94.73%

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.
Humulus lupulus

Cross-Links

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PubChem 10778
NPASS NPC133044