2,3,6-Trimethylbenzoic acid

Details

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Internal ID b9e97301-364e-44e7-ac2b-cdd7faa74379
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acids
IUPAC Name 2,3,6-trimethylbenzoic acid
SMILES (Canonical) CC1=C(C(=C(C=C1)C)C(=O)O)C
SMILES (Isomeric) CC1=C(C(=C(C=C1)C)C(=O)O)C
InChI InChI=1S/C10H12O2/c1-6-4-5-7(2)9(8(6)3)10(11)12/h4-5H,1-3H3,(H,11,12)
InChI Key JRUKSSBDIZXQDX-UHFFFAOYSA-N
Popularity 4 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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2529-36-4
2535-06-0
Benzoic acid, 2,3,6-trimethyl-
2,3,6-Trimethyl-benzoic acid
SCHEMBL1257806
DTXSID60179928
JRUKSSBDIZXQDX-UHFFFAOYSA-N
2,3,6-TRIMETHYLBENZOICACID
CAA52936
AKOS022636810
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,3,6-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 + 0.9257 92.57%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.8389 83.89%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9670 96.70%
OATP1B3 inhibitior + 0.9625 96.25%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8560 85.60%
P-glycoprotein inhibitior - 0.9701 97.01%
P-glycoprotein substrate - 0.9833 98.33%
CYP3A4 substrate - 0.8005 80.05%
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 - 0.9500 95.00%
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 + 0.9667 96.67%
Skin irritation + 0.9002 90.02%
Skin corrosion - 0.6266 62.66%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7648 76.48%
Micronuclear - 0.8267 82.67%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation + 0.6480 64.80%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity + 0.5947 59.47%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.5129 51.29%
Acute Oral Toxicity (c) III 0.6833 68.33%
Estrogen receptor binding - 0.8326 83.26%
Androgen receptor binding - 0.7862 78.62%
Thyroid receptor binding - 0.7979 79.79%
Glucocorticoid receptor binding - 0.9248 92.48%
Aromatase binding - 0.8580 85.80%
PPAR gamma - 0.7185 71.85%
Honey bee toxicity - 0.9955 99.55%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.8000 80.00%
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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.86% 95.56%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.26% 93.56%
CHEMBL2581 P07339 Cathepsin D 84.93% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.92% 96.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 82.34% 81.11%
CHEMBL3401 O75469 Pregnane X receptor 80.39% 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.
Molopospermum peloponnesiacum

Cross-Links

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PubChem 17314
LOTUS LTS0236526
wikiData Q105337952