2,3,4-Trimethylbenzoic acid

Details

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Internal ID c0b4949a-d847-4a55-a75e-2421339dafd1
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acids
IUPAC Name 2,3,4-trimethylbenzoic acid
SMILES (Canonical) CC1=C(C(=C(C=C1)C(=O)O)C)C
SMILES (Isomeric) CC1=C(C(=C(C=C1)C(=O)O)C)C
InChI InChI=1S/C10H12O2/c1-6-4-5-9(10(11)12)8(3)7(6)2/h4-5H,1-3H3,(H,11,12)
InChI Key HDIJZFORGDBEKL-UHFFFAOYSA-N
Popularity 31 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12O2
Molecular Weight 164.20 g/mol
Exact Mass 164.083729621 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.31
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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1076-47-7
2,3,4-TRIMETHYLBENZOICACID
Benzoic acid, 2,3,4-trimethyl-
trimethylbenzoic acid
SCHEMBL242262
2,3,4-Trimethyl-benzoic acid
DTXSID80148111
MFCD20638198
AKOS022636802
AS-47036
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,3,4-Trimethylbenzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9956 99.56%
Caco-2 + 0.9115 91.15%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.8389 83.89%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9727 97.27%
OATP1B3 inhibitior + 0.9625 96.25%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9233 92.33%
P-glycoprotein inhibitior - 0.9686 96.86%
P-glycoprotein substrate - 0.9823 98.23%
CYP3A4 substrate - 0.8281 82.81%
CYP2C9 substrate - 0.6120 61.20%
CYP2D6 substrate - 0.9199 91.99%
CYP3A4 inhibition - 0.9646 96.46%
CYP2C9 inhibition - 0.9640 96.40%
CYP2C19 inhibition - 0.9871 98.71%
CYP2D6 inhibition - 0.9484 94.84%
CYP1A2 inhibition - 0.8584 85.84%
CYP2C8 inhibition - 0.9381 93.81%
CYP inhibitory promiscuity - 0.9528 95.28%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5034 50.34%
Carcinogenicity (trinary) Non-required 0.7565 75.65%
Eye corrosion + 0.6470 64.70%
Eye irritation + 0.9803 98.03%
Skin irritation + 0.9002 90.02%
Skin corrosion - 0.6266 62.66%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8040 80.40%
Micronuclear - 0.8267 82.67%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation + 0.6480 64.80%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity + 0.5947 59.47%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.5586 55.86%
Acute Oral Toxicity (c) III 0.6833 68.33%
Estrogen receptor binding - 0.8497 84.97%
Androgen receptor binding - 0.7783 77.83%
Thyroid receptor binding - 0.8295 82.95%
Glucocorticoid receptor binding - 0.8879 88.79%
Aromatase binding - 0.8781 87.81%
PPAR gamma - 0.8843 88.43%
Honey bee toxicity - 0.9928 99.28%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.9000 90.00%
Fish aquatic toxicity + 0.9454 94.54%

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
CHEMBL1293277 O15118 Niemann-Pick C1 protein 92.33% 81.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.30% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.29% 98.95%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 88.54% 87.67%
CHEMBL5847 P52895 Aldo-keto reductase family 1 member C2 84.26% 92.50%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.21% 93.00%

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.
Molopospermum peloponnesiacum

Cross-Links

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PubChem 14103
LOTUS LTS0195190
wikiData Q83013563