Ethyl butyrate

Details

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Internal ID 9238bd39-f024-4ef0-80fc-80cffc8bec4b
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name ethyl butanoate
SMILES (Canonical) CCCC(=O)OCC
SMILES (Isomeric) CCCC(=O)OCC
InChI InChI=1S/C6H12O2/c1-3-5-6(7)8-4-2/h3-5H2,1-2H3
InChI Key OBNCKNCVKJNDBV-UHFFFAOYSA-N
Popularity 1,748 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 1.30
Atomic LogP (AlogP) 1.35
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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Ethyl butanoate
105-54-4
Butyric acid ethyl ester
Ethyl n-butyrate
Butanoic acid, ethyl ester
Ethyl n-butanoate
Butyric ester
Butyric ether
Butanoic acid ethyl ester
Butyric acid, ethyl ester
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 butyrate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 + 0.9047 90.47%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.6108 61.08%
OATP2B1 inhibitior - 0.8331 83.31%
OATP1B1 inhibitior + 0.9418 94.18%
OATP1B3 inhibitior + 0.9297 92.97%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9354 93.54%
P-glycoprotein inhibitior - 0.9898 98.98%
P-glycoprotein substrate - 0.9907 99.07%
CYP3A4 substrate - 0.6539 65.39%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8679 86.79%
CYP3A4 inhibition - 0.9575 95.75%
CYP2C9 inhibition - 0.9280 92.80%
CYP2C19 inhibition - 0.9471 94.71%
CYP2D6 inhibition - 0.9209 92.09%
CYP1A2 inhibition - 0.5758 57.58%
CYP2C8 inhibition - 0.9699 96.99%
CYP inhibitory promiscuity - 0.8239 82.39%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.5696 56.96%
Eye corrosion + 0.9854 98.54%
Eye irritation + 0.9949 99.49%
Skin irritation - 0.7341 73.41%
Skin corrosion - 0.9960 99.60%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7504 75.04%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5767 57.67%
skin sensitisation + 0.7236 72.36%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.4916 49.16%
Acute Oral Toxicity (c) IV 0.4884 48.84%
Estrogen receptor binding - 0.9539 95.39%
Androgen receptor binding - 0.9746 97.46%
Thyroid receptor binding - 0.9240 92.40%
Glucocorticoid receptor binding - 0.9410 94.10%
Aromatase binding - 0.9050 90.50%
PPAR gamma - 0.9303 93.03%
Honey bee toxicity - 0.9491 94.91%
Biodegradation + 0.9500 95.00%
Crustacea aquatic toxicity + 0.5145 51.45%
Fish aquatic toxicity + 0.8890 88.90%

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 91.79% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.49% 99.17%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.66% 97.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.47% 96.95%
CHEMBL230 P35354 Cyclooxygenase-2 82.81% 89.63%
CHEMBL221 P23219 Cyclooxygenase-1 81.48% 90.17%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.69% 94.33%

Cross-Links

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PubChem 7762
NPASS NPC143211
LOTUS LTS0106732
wikiData Q412270