4-Ethyltoluene

Details

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Internal ID 095b6d42-bf67-4393-83d8-bdb4e9797336
Taxonomy Benzenoids > Benzene and substituted derivatives > Toluenes
IUPAC Name 1-ethyl-4-methylbenzene
SMILES (Canonical) CCC1=CC=C(C=C1)C
SMILES (Isomeric) CCC1=CC=C(C=C1)C
InChI InChI=1S/C9H12/c1-3-9-6-4-8(2)5-7-9/h4-7H,3H2,1-2H3
InChI Key JRLPEMVDPFPYPJ-UHFFFAOYSA-N
Popularity 379 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 3.60
Atomic LogP (AlogP) 2.56
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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1-Ethyl-4-methylbenzene
622-96-8
P-ETHYLTOLUENE
Benzene, 1-ethyl-4-methyl-
Toluene, p-ethyl-
4-Methylethylbenzene
p-Ethylmethylbenzene
p-Methylethylbenzene
1-Methyl-4-ethylbenzene
1-Ethyl-4-methyl-benzene
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-Ethyltoluene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9951 99.51%
Caco-2 + 0.9826 98.26%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.9000 90.00%
Subcellular localzation Lysosomes 0.5263 52.63%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9517 95.17%
OATP1B3 inhibitior + 0.9563 95.63%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8262 82.62%
P-glycoprotein inhibitior - 0.9856 98.56%
P-glycoprotein substrate - 0.9756 97.56%
CYP3A4 substrate - 0.7883 78.83%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3634 36.34%
CYP3A4 inhibition - 0.9417 94.17%
CYP2C9 inhibition - 0.8933 89.33%
CYP2C19 inhibition - 0.8870 88.70%
CYP2D6 inhibition - 0.9068 90.68%
CYP1A2 inhibition - 0.6414 64.14%
CYP2C8 inhibition - 0.9367 93.67%
CYP inhibitory promiscuity - 0.6442 64.42%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5981 59.81%
Carcinogenicity (trinary) Warning 0.5215 52.15%
Eye corrosion + 0.9901 99.01%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.8986 89.86%
Skin corrosion - 0.9568 95.68%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6098 60.98%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7574 75.74%
skin sensitisation + 0.9827 98.27%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.7287 72.87%
Acute Oral Toxicity (c) III 0.8477 84.77%
Estrogen receptor binding - 0.9333 93.33%
Androgen receptor binding - 0.7889 78.89%
Thyroid receptor binding - 0.8802 88.02%
Glucocorticoid receptor binding - 0.8992 89.92%
Aromatase binding - 0.7694 76.94%
PPAR gamma - 0.9172 91.72%
Honey bee toxicity - 0.9513 95.13%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.8300 83.00%
Fish aquatic toxicity + 0.9187 91.87%

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
CHEMBL2581 P07339 Cathepsin D 93.48% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.03% 96.09%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.26% 93.65%
CHEMBL221 P23219 Cyclooxygenase-1 84.17% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 83.76% 94.73%
CHEMBL3769292 Q9H773 dCTP pyrophosphatase 1 83.32% 94.40%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.37% 90.24%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.08% 95.56%

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.
Chaenomeles sinensis
Crocus sativus
Gossypium hirsutum
Humulus lupulus
Sophora flavescens

Cross-Links

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PubChem 12160
NPASS NPC248705
LOTUS LTS0062409
wikiData Q24300547