Ethyl isobutyrate

Details

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Internal ID 7a4b8b12-7411-4440-be21-d70b8b1d80a9
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Carboxylic acid esters
IUPAC Name ethyl 2-methylpropanoate
SMILES (Canonical) CCOC(=O)C(C)C
SMILES (Isomeric) CCOC(=O)C(C)C
InChI InChI=1S/C6H12O2/c1-4-8-6(7)5(2)3/h5H,4H2,1-3H3
InChI Key WDAXFOBOLVPGLV-UHFFFAOYSA-N
Popularity 367 references in papers

Physical and Chemical Properties

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Molecular Formula C6H12O2
Molecular Weight 116.16 g/mol
Exact Mass 116.083729621 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.21
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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97-62-1
Ethyl 2-methylpropanoate
Isobutyric acid ethyl ester
Ethylisobutyrate
Ethyl isobutanoate
Propanoic acid, 2-methyl-, ethyl ester
Ethyl 2,2-dimethylacetate
Isobutyric acid, ethyl ester
Ethyl 2-methylpropionate
FEMA No. 2428
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Ethyl isobutyrate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9965 99.65%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7044 70.44%
OATP2B1 inhibitior - 0.8560 85.60%
OATP1B1 inhibitior + 0.9608 96.08%
OATP1B3 inhibitior + 0.9471 94.71%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9119 91.19%
P-glycoprotein inhibitior - 0.9849 98.49%
P-glycoprotein substrate - 0.9959 99.59%
CYP3A4 substrate - 0.7187 71.87%
CYP2C9 substrate - 0.6168 61.68%
CYP2D6 substrate - 0.8859 88.59%
CYP3A4 inhibition - 0.9811 98.11%
CYP2C9 inhibition - 0.9346 93.46%
CYP2C19 inhibition - 0.9620 96.20%
CYP2D6 inhibition - 0.9568 95.68%
CYP1A2 inhibition - 0.8084 80.84%
CYP2C8 inhibition - 0.9944 99.44%
CYP inhibitory promiscuity - 0.8390 83.90%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5874 58.74%
Carcinogenicity (trinary) Non-required 0.5158 51.58%
Eye corrosion + 0.9856 98.56%
Eye irritation + 0.9941 99.41%
Skin irritation + 0.7226 72.26%
Skin corrosion - 0.9295 92.95%
Ames mutagenesis - 0.9600 96.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7480 74.80%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6384 63.84%
skin sensitisation + 0.5838 58.38%
Respiratory toxicity - 0.9778 97.78%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.6195 61.95%
Acute Oral Toxicity (c) III 0.5012 50.12%
Estrogen receptor binding - 0.9154 91.54%
Androgen receptor binding - 0.8458 84.58%
Thyroid receptor binding - 0.9290 92.90%
Glucocorticoid receptor binding - 0.9240 92.40%
Aromatase binding - 0.7809 78.09%
PPAR gamma - 0.9337 93.37%
Honey bee toxicity - 0.9300 93.00%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.8255 82.55%
Fish aquatic toxicity + 0.7069 70.69%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.82% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.23% 96.95%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 86.21% 96.47%
CHEMBL2581 P07339 Cathepsin D 85.67% 98.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.06% 97.21%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.21% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 81.11% 94.73%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 81.02% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.70% 99.17%

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.
Heracleum dissectum
Hippophae rhamnoides
Humulus lupulus
Vaccinium angustifolium
Vitis vinifera

Cross-Links

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PubChem 7342
NPASS NPC233567
LOTUS LTS0162364
wikiData Q27159510