1,2,4-Trimethylbenzene

Details

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Internal ID da046b97-d7bd-4c80-851e-a3090051670e
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 1,2,4-trimethylbenzene
SMILES (Canonical) CC1=CC(=C(C=C1)C)C
SMILES (Isomeric) CC1=CC(=C(C=C1)C)C
InChI InChI=1S/C9H12/c1-7-4-5-8(2)9(3)6-7/h4-6H,1-3H3
InChI Key GWHJZXXIDMPWGX-UHFFFAOYSA-N
Popularity 1,543 references in papers

Physical and Chemical Properties

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Molecular Formula C9H12
Molecular Weight 120.19 g/mol
Exact Mass 120.093900383 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.61
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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Pseudocumene
95-63-6
Pseudocumol
Psi-cumene
as-Trimethylbenzene
1,3,4-Trimethylbenzene
Benzene, 1,2,4-trimethyl-
Uns-trimethylbenzene
1,2,5-Trimethylbenzene
Asymmetrical trimethylbenzene
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,2,4-Trimethylbenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9944 99.44%
Caco-2 + 0.9134 91.34%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.8857 88.57%
Subcellular localzation Mitochondria 0.5629 56.29%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9744 97.44%
OATP1B3 inhibitior + 0.9633 96.33%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8673 86.73%
P-glycoprotein inhibitior - 0.9825 98.25%
P-glycoprotein substrate - 0.9777 97.77%
CYP3A4 substrate - 0.8067 80.67%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7340 73.40%
CYP3A4 inhibition - 0.9374 93.74%
CYP2C9 inhibition - 0.9261 92.61%
CYP2C19 inhibition - 0.8939 89.39%
CYP2D6 inhibition - 0.9356 93.56%
CYP1A2 inhibition - 0.6775 67.75%
CYP2C8 inhibition - 0.9538 95.38%
CYP inhibitory promiscuity - 0.6329 63.29%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5300 53.00%
Carcinogenicity (trinary) Warning 0.5220 52.20%
Eye corrosion + 0.9721 97.21%
Eye irritation + 0.9943 99.43%
Skin irritation + 0.9313 93.13%
Skin corrosion - 0.9713 97.13%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6610 66.10%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation + 0.9512 95.12%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity - 0.5536 55.36%
Acute Oral Toxicity (c) III 0.6305 63.05%
Estrogen receptor binding - 0.9178 91.78%
Androgen receptor binding - 0.8476 84.76%
Thyroid receptor binding - 0.8242 82.42%
Glucocorticoid receptor binding - 0.8722 87.22%
Aromatase binding - 0.7918 79.18%
PPAR gamma - 0.9115 91.15%
Honey bee toxicity - 0.9833 98.33%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.8500 85.00%
Fish aquatic toxicity + 0.9604 96.04%

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
CHEMBL2039 P27338 Monoamine oxidase B 88.16% 92.51%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.65% 95.56%
CHEMBL1913 P09619 Platelet-derived growth factor receptor beta 87.44% 95.70%
CHEMBL2581 P07339 Cathepsin D 86.46% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 85.31% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.86% 93.65%
CHEMBL4581 P52732 Kinesin-like protein 1 83.66% 93.18%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 83.30% 90.93%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.87% 96.00%

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.
Artemisia argyi
Artemisia montana
Artemisia princeps
Seriphidium herba-alba

Cross-Links

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PubChem 7247
NPASS NPC6107
LOTUS LTS0168666
wikiData Q376994