1-Ethyl-3,5-dimethylbenzene

Details

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Internal ID 88572c2c-3d24-478a-8e43-37aa65ba6f69
Taxonomy Benzenoids > Benzene and substituted derivatives > Xylenes > m-Xylenes
IUPAC Name 1-ethyl-3,5-dimethylbenzene
SMILES (Canonical) CCC1=CC(=CC(=C1)C)C
SMILES (Isomeric) CCC1=CC(=CC(=C1)C)C
InChI InChI=1S/C10H14/c1-4-10-6-8(2)5-9(3)7-10/h5-7H,4H2,1-3H3
InChI Key LMAUULKNZLEMGN-UHFFFAOYSA-N
Popularity 36 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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5-Ethyl-m-xylene
934-74-7
1,3-DIMETHYL-5-ETHYLBENZENE
m-Xylene, 5-ethyl-
Benzene, 1-ethyl-3,5-dimethyl-
5-ethyl-1,3-dimethylbenzene
WQH822L3HK
EINECS 213-290-0
NSC 74185
NSC-74185
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-Ethyl-3,5-dimethylbenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9949 99.49%
Caco-2 + 0.9323 93.23%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Lysosomes 0.5998 59.98%
OATP2B1 inhibitior - 0.8660 86.60%
OATP1B1 inhibitior + 0.9248 92.48%
OATP1B3 inhibitior + 0.9419 94.19%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8005 80.05%
P-glycoprotein inhibitior - 0.9829 98.29%
P-glycoprotein substrate - 0.9782 97.82%
CYP3A4 substrate - 0.7792 77.92%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3634 36.34%
CYP3A4 inhibition - 0.9438 94.38%
CYP2C9 inhibition - 0.9053 90.53%
CYP2C19 inhibition - 0.9269 92.69%
CYP2D6 inhibition - 0.9136 91.36%
CYP1A2 inhibition - 0.6965 69.65%
CYP2C8 inhibition - 0.9457 94.57%
CYP inhibitory promiscuity - 0.5750 57.50%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5981 59.81%
Carcinogenicity (trinary) Warning 0.5351 53.51%
Eye corrosion + 0.9582 95.82%
Eye irritation + 0.9855 98.55%
Skin irritation + 0.8612 86.12%
Skin corrosion - 0.9332 93.32%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5888 58.88%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation + 0.9659 96.59%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.7663 76.63%
Acute Oral Toxicity (c) III 0.8896 88.96%
Estrogen receptor binding - 0.9634 96.34%
Androgen receptor binding - 0.6951 69.51%
Thyroid receptor binding - 0.8592 85.92%
Glucocorticoid receptor binding - 0.8822 88.22%
Aromatase binding - 0.8735 87.35%
PPAR gamma - 0.9062 90.62%
Honey bee toxicity - 0.9515 95.15%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9322 93.22%

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 91.54% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.06% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 86.95% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.46% 86.33%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.25% 93.65%

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
Atractylodes lancea
Atractylodes macrocephala

Cross-Links

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PubChem 13627
NPASS NPC33407