1-Ethyl-2,3-dimethylbenzene

Details

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Internal ID a97000db-9014-4fac-84fe-0ddd7fd77ce4
Taxonomy Benzenoids > Benzene and substituted derivatives > Xylenes > o-Xylenes
IUPAC Name 1-ethyl-2,3-dimethylbenzene
SMILES (Canonical) CCC1=CC=CC(=C1C)C
SMILES (Isomeric) CCC1=CC=CC(=C1C)C
InChI InChI=1S/C10H14/c1-4-10-7-5-6-8(2)9(10)3/h5-7H,4H2,1-3H3
InChI Key QUBBAXISAHIDNM-UHFFFAOYSA-N
Popularity 81 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 3.90
Atomic LogP (AlogP) 2.87
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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3-Ethyl-o-xylene
933-98-2
1,2-DIMETHYL-3-ETHYLBENZENE
Ethylxylene
Benzene, 1-ethyl-2,3-dimethyl-
o-Xylene, 3-ethyl-
Benzene, ethyldimethyl-
Ethyldimethylbenzene
29224-55-3
3-Ethyl-1,2-dimethylbenzene
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-2,3-dimethylbenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 + 0.9524 95.24%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Lysosomes 0.4964 49.64%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9651 96.51%
OATP1B3 inhibitior + 0.9404 94.04%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8559 85.59%
P-glycoprotein inhibitior - 0.9901 99.01%
P-glycoprotein substrate - 0.9454 94.54%
CYP3A4 substrate - 0.7437 74.37%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3634 36.34%
CYP3A4 inhibition - 0.9605 96.05%
CYP2C9 inhibition - 0.8918 89.18%
CYP2C19 inhibition - 0.8432 84.32%
CYP2D6 inhibition - 0.8983 89.83%
CYP1A2 inhibition - 0.6353 63.53%
CYP2C8 inhibition - 0.9272 92.72%
CYP inhibitory promiscuity + 0.5125 51.25%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5300 53.00%
Carcinogenicity (trinary) Non-required 0.4490 44.90%
Eye corrosion + 0.8122 81.22%
Eye irritation + 0.9614 96.14%
Skin irritation + 0.8580 85.80%
Skin corrosion - 0.9293 92.93%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6380 63.80%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation + 0.9564 95.64%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.7556 75.56%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.4865 48.65%
Acute Oral Toxicity (c) III 0.7661 76.61%
Estrogen receptor binding - 0.9497 94.97%
Androgen receptor binding - 0.7833 78.33%
Thyroid receptor binding - 0.8740 87.40%
Glucocorticoid receptor binding - 0.8918 89.18%
Aromatase binding - 0.8783 87.83%
PPAR gamma - 0.9165 91.65%
Honey bee toxicity - 0.9832 98.32%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9884 98.84%

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 93.49% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 91.39% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.99% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.39% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.49% 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
Hansenia forbesii
Hansenia weberbaueriana

Cross-Links

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PubChem 13621
NPASS NPC4178