1,2-Dimethyl-4-ethylbenzene

Details

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Internal ID 7edd3642-0fc2-4a3c-a2ad-00bc332e7a29
Taxonomy Benzenoids > Benzene and substituted derivatives > Xylenes > o-Xylenes
IUPAC Name 4-ethyl-1,2-dimethylbenzene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14/c1-4-10-6-5-8(2)9(3)7-10/h5-7H,4H2,1-3H3
InChI Key SBUYFICWQNHBCM-UHFFFAOYSA-N
Popularity 61 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14
Molecular Weight 134.22 g/mol
Exact Mass 134.109550447 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.87
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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4-Ethyl-o-xylene
1,2-Dimethyl-4-ethylbenzene
1-ethyl-3,4-dimethylbenzene
S21X4T3N1G
EINECS 213-293-7
NSC 74183
NSC-74183
UNII-S21X4T3N1G
1,2-Dimethyl-4-ethyl benzene
DTXSID6061317
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-Dimethyl-4-ethylbenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 + 0.9467 94.67%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Mitochondria 0.5129 51.29%
OATP2B1 inhibitior - 0.8686 86.86%
OATP1B1 inhibitior + 0.9598 95.98%
OATP1B3 inhibitior + 0.9444 94.44%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8366 83.66%
P-glycoprotein inhibitior - 0.9842 98.42%
P-glycoprotein substrate - 0.9263 92.63%
CYP3A4 substrate - 0.7634 76.34%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3634 36.34%
CYP3A4 inhibition - 0.9582 95.82%
CYP2C9 inhibition - 0.8779 87.79%
CYP2C19 inhibition - 0.8327 83.27%
CYP2D6 inhibition - 0.9105 91.05%
CYP1A2 inhibition - 0.6228 62.28%
CYP2C8 inhibition - 0.8209 82.09%
CYP inhibitory promiscuity + 0.5915 59.15%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5500 55.00%
Carcinogenicity (trinary) Warning 0.4835 48.35%
Eye corrosion + 0.8861 88.61%
Eye irritation + 0.9905 99.05%
Skin irritation + 0.8336 83.36%
Skin corrosion - 0.9610 96.10%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5421 54.21%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation + 0.9634 96.34%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.8625 86.25%
Acute Oral Toxicity (c) III 0.8381 83.81%
Estrogen receptor binding - 0.9397 93.97%
Androgen receptor binding - 0.7318 73.18%
Thyroid receptor binding - 0.8691 86.91%
Glucocorticoid receptor binding - 0.8712 87.12%
Aromatase binding - 0.7512 75.12%
PPAR gamma - 0.9214 92.14%
Honey bee toxicity - 0.9553 95.53%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.9746 97.46%

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 94.42% 98.95%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 88.85% 93.65%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 87.14% 90.75%
CHEMBL3401 O75469 Pregnane X receptor 85.81% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.22% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.23% 86.33%
CHEMBL3492 P49721 Proteasome Macropain subunit 80.73% 90.24%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.47% 96.00%
CHEMBL2073 P07947 Tyrosine-protein kinase YES 80.40% 83.14%

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
Cinnamomum aromaticum
Cornus officinalis
Foeniculum vulgare

Cross-Links

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PubChem 13629
NPASS NPC231559