p-Tolyl acetate

Details

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Internal ID 8b0a0eec-0664-4cbc-818c-0a20c996c3e6
Taxonomy Benzenoids > Phenol esters
IUPAC Name (4-methylphenyl) acetate
SMILES (Canonical) CC1=CC=C(C=C1)OC(=O)C
SMILES (Isomeric) CC1=CC=C(C=C1)OC(=O)C
InChI InChI=1S/C9H10O2/c1-7-3-5-9(6-4-7)11-8(2)10/h3-6H,1-2H3
InChI Key CDJJKTLOZJAGIZ-UHFFFAOYSA-N
Popularity 97 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 2.10
Atomic LogP (AlogP) 1.92
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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p-Cresyl acetate
140-39-6
Acetic acid, 4-methylphenyl ester
4-Tolyl acetate
p-Acetoxytoluene
4-Methylphenyl acetate
Narceol
4-Acetoxytoluene
p-Cresol acetate
Cresyl acetate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of p-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 + 0.9405 94.05%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.8853 88.53%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9752 97.52%
OATP1B3 inhibitior + 0.9763 97.63%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.7391 73.91%
P-glycoprotein inhibitior - 0.9886 98.86%
P-glycoprotein substrate - 0.9948 99.48%
CYP3A4 substrate - 0.6715 67.15%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.8564 85.64%
CYP3A4 inhibition - 0.9598 95.98%
CYP2C9 inhibition - 0.9605 96.05%
CYP2C19 inhibition - 0.8657 86.57%
CYP2D6 inhibition - 0.9692 96.92%
CYP1A2 inhibition + 0.6471 64.71%
CYP2C8 inhibition - 0.9678 96.78%
CYP inhibitory promiscuity - 0.8511 85.11%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5960 59.60%
Carcinogenicity (trinary) Non-required 0.6007 60.07%
Eye corrosion + 0.9468 94.68%
Eye irritation + 0.9956 99.56%
Skin irritation + 0.7731 77.31%
Skin corrosion - 0.9158 91.58%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7406 74.06%
Micronuclear - 0.7826 78.26%
Hepatotoxicity + 0.7409 74.09%
skin sensitisation + 0.7004 70.04%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.8226 82.26%
Acute Oral Toxicity (c) III 0.9503 95.03%
Estrogen receptor binding - 0.9248 92.48%
Androgen receptor binding - 0.7984 79.84%
Thyroid receptor binding - 0.8265 82.65%
Glucocorticoid receptor binding - 0.9175 91.75%
Aromatase binding - 0.7797 77.97%
PPAR gamma - 0.8544 85.44%
Honey bee toxicity - 0.8926 89.26%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.8885 88.85%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL1293235 P02545 Prelamin-A/C 12589.3 nM
Potency
via CMAUP

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.34% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.35% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.44% 91.11%
CHEMBL2581 P07339 Cathepsin D 86.71% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 84.27% 94.73%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.19% 94.80%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 81.90% 81.11%

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.
Conioselinum anthriscoides
Ligusticum officinale
Ligusticum striatum
Prunus mume

Cross-Links

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PubChem 8797
NPASS NPC107101
ChEMBL CHEMBL501246