4-Methylbenzoic acid

Details

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Internal ID 62be690c-78e8-40f9-a4dd-8c1928fc8acf
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acids
IUPAC Name 4-methylbenzoic acid
SMILES (Canonical) CC1=CC=C(C=C1)C(=O)O
SMILES (Isomeric) CC1=CC=C(C=C1)C(=O)O
InChI InChI=1S/C8H8O2/c1-6-2-4-7(5-3-6)8(9)10/h2-5H,1H3,(H,9,10)
InChI Key LPNBBFKOUUSUDB-UHFFFAOYSA-N
Popularity 796 references in papers

Physical and Chemical Properties

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Molecular Formula C8H8O2
Molecular Weight 136.15 g/mol
Exact Mass 136.052429494 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.69
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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P-TOLUIC ACID
99-94-5
4-Toluic acid
p-Methylbenzoic acid
Benzoic acid, 4-methyl-
Crithminic acid
p-Toluylic acid
p-Carboxytoluene
para-Toluic acid
4-Methyl-Benzoic 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-Methylbenzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.9478 94.78%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Mitochondria 0.6943 69.43%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9686 96.86%
OATP1B3 inhibitior + 0.9704 97.04%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9252 92.52%
P-glycoprotein inhibitior - 0.9797 97.97%
P-glycoprotein substrate - 0.9940 99.40%
CYP3A4 substrate - 0.8390 83.90%
CYP2C9 substrate + 0.5512 55.12%
CYP2D6 substrate - 0.9035 90.35%
CYP3A4 inhibition - 0.9775 97.75%
CYP2C9 inhibition - 0.9780 97.80%
CYP2C19 inhibition - 0.9918 99.18%
CYP2D6 inhibition - 0.9674 96.74%
CYP1A2 inhibition - 0.8782 87.82%
CYP2C8 inhibition - 0.9375 93.75%
CYP inhibitory promiscuity - 0.9875 98.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5279 52.79%
Carcinogenicity (trinary) Non-required 0.7505 75.05%
Eye corrosion + 0.9272 92.72%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.9732 97.32%
Skin corrosion + 0.9671 96.71%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9260 92.60%
Micronuclear - 0.8141 81.41%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation + 0.5381 53.81%
Respiratory toxicity - 0.9000 90.00%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.6591 65.91%
Acute Oral Toxicity (c) III 0.6756 67.56%
Estrogen receptor binding - 0.8988 89.88%
Androgen receptor binding - 0.8743 87.43%
Thyroid receptor binding - 0.8823 88.23%
Glucocorticoid receptor binding - 0.9234 92.34%
Aromatase binding - 0.8744 87.44%
PPAR gamma - 0.8664 86.64%
Honey bee toxicity - 0.9952 99.52%
Biodegradation + 0.9250 92.50%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity + 0.8205 82.05%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL3577 P00352 Aldehyde dehydrogenase 1A1 25118.9 nM
Potency
via CMAUP
CHEMBL1293232 Q16637 Survival motor neuron protein 100 nM
100 nM
Potency
Potency
via CMAUP
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL1293294 P51151 Ras-related protein Rab-9A 96.56% 87.67%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 94.65% 81.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.14% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.92% 86.33%

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.
Aloe africana
Aloe ferox
Aloe spicata
Aloe vera
Artemisia afra
Crataegus pinnatifida

Cross-Links

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PubChem 7470
NPASS NPC253423
ChEMBL CHEMBL21708
LOTUS LTS0189538
wikiData Q1607905