3-Ethyltoluene

Details

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Internal ID 05213aec-165e-4e02-8aab-3cbc68254a23
Taxonomy Benzenoids > Benzene and substituted derivatives > Toluenes
IUPAC Name 1-ethyl-3-methylbenzene
SMILES (Canonical) CCC1=CC=CC(=C1)C
SMILES (Isomeric) CCC1=CC=CC(=C1)C
InChI InChI=1S/C9H12/c1-3-9-6-4-5-8(2)7-9/h4-7H,3H2,1-2H3
InChI Key ZLCSFXXPPANWQY-UHFFFAOYSA-N
Popularity 311 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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620-14-4
1-Ethyl-3-methylbenzene
M-ETHYLTOLUENE
1-Methyl-3-ethylbenzene
Benzene, 1-ethyl-3-methyl-
m-Ethylmethylbenzene
m-Methylethylbenzene
Toluene, m-ethyl-
3-Methylethylbenzene
NSC 74176
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Ethyltoluene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.9464 94.64%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8857 88.57%
Subcellular localzation Lysosomes 0.6065 60.65%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9520 95.20%
OATP1B3 inhibitior + 0.9429 94.29%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8310 83.10%
P-glycoprotein inhibitior - 0.9913 99.13%
P-glycoprotein substrate - 0.9395 93.95%
CYP3A4 substrate - 0.7313 73.13%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3634 36.34%
CYP3A4 inhibition - 0.9599 95.99%
CYP2C9 inhibition - 0.8985 89.85%
CYP2C19 inhibition - 0.9045 90.45%
CYP2D6 inhibition - 0.9139 91.39%
CYP1A2 inhibition - 0.6620 66.20%
CYP2C8 inhibition - 0.8303 83.03%
CYP inhibitory promiscuity - 0.6270 62.70%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6181 61.81%
Carcinogenicity (trinary) Warning 0.4911 49.11%
Eye corrosion + 0.9804 98.04%
Eye irritation + 0.9912 99.12%
Skin irritation + 0.8699 86.99%
Skin corrosion - 0.9575 95.75%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6143 61.43%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation + 0.9801 98.01%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.8386 83.86%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity - 0.7632 76.32%
Acute Oral Toxicity (c) III 0.8815 88.15%
Estrogen receptor binding - 0.9677 96.77%
Androgen receptor binding - 0.8333 83.33%
Thyroid receptor binding - 0.9055 90.55%
Glucocorticoid receptor binding - 0.8999 89.99%
Aromatase binding - 0.9031 90.31%
PPAR gamma - 0.9119 91.19%
Honey bee toxicity - 0.9749 97.49%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9311 93.11%

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 96.64% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 91.97% 94.73%
CHEMBL221 P23219 Cyclooxygenase-1 88.98% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.74% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.15% 96.09%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 85.90% 96.42%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.69% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.12% 95.56%
CHEMBL240 Q12809 HERG 84.01% 89.76%
CHEMBL1907 P15144 Aminopeptidase N 81.20% 93.31%

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.
Acorus calamus var. angustatus
Acorus gramineus
Artemisia argyi
Artemisia montana
Artemisia princeps
Chaenomeles sinensis
Gossypium hirsutum

Cross-Links

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PubChem 12100
NPASS NPC150196
LOTUS LTS0183186
wikiData Q27105073