4-Acetylbenzoic acid

Details

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Internal ID 573f650e-e645-4a53-830e-1fd4f2f4707d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 4-acetylbenzoic acid
SMILES (Canonical) CC(=O)C1=CC=C(C=C1)C(=O)O
SMILES (Isomeric) CC(=O)C1=CC=C(C=C1)C(=O)O
InChI InChI=1S/C9H8O3/c1-6(10)7-2-4-8(5-3-7)9(11)12/h2-5H,1H3,(H,11,12)
InChI Key QBHDSQZASIBAAI-UHFFFAOYSA-N
Popularity 47 references in papers

Physical and Chemical Properties

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Molecular Formula C9H8O3
Molecular Weight 164.16 g/mol
Exact Mass 164.047344113 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.59
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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586-89-0
Benzoic acid, 4-acetyl-
4-Acetyl-benzoic acid
p-acetylbenzoic acid
4-Acetylbenzoci acid
MFCD00002561
EINECS 209-588-5
4-Acetylbenzoicacid
Acetophenone-4-carboxylic acid
4'-Acetophenonecarboxylic Acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Acetylbenzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9888 98.88%
Caco-2 + 0.9003 90.03%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.9076 90.76%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9715 97.15%
OATP1B3 inhibitior + 0.9735 97.35%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8843 88.43%
P-glycoprotein inhibitior - 0.9836 98.36%
P-glycoprotein substrate - 0.9854 98.54%
CYP3A4 substrate - 0.8353 83.53%
CYP2C9 substrate + 0.5538 55.38%
CYP2D6 substrate - 0.8857 88.57%
CYP3A4 inhibition - 0.9778 97.78%
CYP2C9 inhibition - 0.9752 97.52%
CYP2C19 inhibition - 0.9866 98.66%
CYP2D6 inhibition - 0.9656 96.56%
CYP1A2 inhibition - 0.9751 97.51%
CYP2C8 inhibition - 0.9385 93.85%
CYP inhibitory promiscuity - 0.9883 98.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5081 50.81%
Carcinogenicity (trinary) Non-required 0.7432 74.32%
Eye corrosion + 0.7149 71.49%
Eye irritation + 0.9970 99.70%
Skin irritation + 0.9070 90.70%
Skin corrosion + 0.7876 78.76%
Ames mutagenesis - 0.9600 96.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9196 91.96%
Micronuclear - 0.7141 71.41%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.5846 58.46%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.6372 63.72%
Acute Oral Toxicity (c) II 0.6278 62.78%
Estrogen receptor binding - 0.9170 91.70%
Androgen receptor binding - 0.8243 82.43%
Thyroid receptor binding - 0.8411 84.11%
Glucocorticoid receptor binding - 0.9354 93.54%
Aromatase binding - 0.7879 78.79%
PPAR gamma - 0.8946 89.46%
Honey bee toxicity - 0.9870 98.70%
Biodegradation + 0.9500 95.00%
Crustacea aquatic toxicity - 0.9600 96.00%
Fish aquatic toxicity + 0.8514 85.14%

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
CHEMBL1293294 P51151 Ras-related protein Rab-9A 94.15% 87.67%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 89.53% 81.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.61% 86.33%
CHEMBL4208 P20618 Proteasome component C5 85.14% 90.00%
CHEMBL2581 P07339 Cathepsin D 81.62% 98.95%

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.
Citrus × aurantium
Citrus deliciosa

Cross-Links

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PubChem 11470
NPASS NPC25458