Methyl butyrate

Details

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Internal ID d8dbd9eb-ac2d-4248-a8ca-2e9af22603ef
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters > Fatty acid methyl esters
IUPAC Name methyl butanoate
SMILES (Canonical) CCCC(=O)OC
SMILES (Isomeric) CCCC(=O)OC
InChI InChI=1S/C5H10O2/c1-3-4-5(6)7-2/h3-4H2,1-2H3
InChI Key UUIQMZJEGPQKFD-UHFFFAOYSA-N
Popularity 1,251 references in papers

Physical and Chemical Properties

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Molecular Formula C5H10O2
Molecular Weight 102.13 g/mol
Exact Mass 102.068079557 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 1.30
Atomic LogP (AlogP) 0.96
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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Methyl butanoate
623-42-7
Butanoic acid, methyl ester
METHYL N-BUTYRATE
Butyric acid, methyl ester
Methyl n-butanoate
Methyl-n-butyrate
Butyric acid methyl ester
n-Butyric acid methyl ester
FEMA No. 2693
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Methyl butyrate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.7931 79.31%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.5086 50.86%
OATP2B1 inhibitior - 0.8564 85.64%
OATP1B1 inhibitior + 0.9402 94.02%
OATP1B3 inhibitior + 0.9138 91.38%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9346 93.46%
P-glycoprotein inhibitior - 0.9889 98.89%
P-glycoprotein substrate - 0.9538 95.38%
CYP3A4 substrate - 0.7162 71.62%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8679 86.79%
CYP3A4 inhibition - 0.9871 98.71%
CYP2C9 inhibition - 0.9495 94.95%
CYP2C19 inhibition - 0.9467 94.67%
CYP2D6 inhibition - 0.9557 95.57%
CYP1A2 inhibition - 0.6332 63.32%
CYP2C8 inhibition - 0.9741 97.41%
CYP inhibitory promiscuity - 0.9327 93.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.6880 68.80%
Eye corrosion + 0.9829 98.29%
Eye irritation + 0.9947 99.47%
Skin irritation + 0.7678 76.78%
Skin corrosion - 0.8730 87.30%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7573 75.73%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6319 63.19%
skin sensitisation + 0.6781 67.81%
Respiratory toxicity - 0.9778 97.78%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.5193 51.93%
Acute Oral Toxicity (c) III 0.8509 85.09%
Estrogen receptor binding - 0.9675 96.75%
Androgen receptor binding - 0.9472 94.72%
Thyroid receptor binding - 0.9267 92.67%
Glucocorticoid receptor binding - 0.9385 93.85%
Aromatase binding - 0.9256 92.56%
PPAR gamma - 0.9162 91.62%
Honey bee toxicity - 0.9627 96.27%
Biodegradation + 0.9000 90.00%
Crustacea aquatic toxicity - 0.5532 55.32%
Fish aquatic toxicity - 0.4199 41.99%

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 94.31% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.31% 99.17%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 85.96% 94.33%
CHEMBL221 P23219 Cyclooxygenase-1 83.58% 90.17%
CHEMBL2581 P07339 Cathepsin D 82.91% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.44% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.38% 96.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.20% 85.14%
CHEMBL4040 P28482 MAP kinase ERK2 80.18% 83.82%

Plants that contains it

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Cross-Links

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PubChem 12180
NPASS NPC28246
LOTUS LTS0013195
wikiData Q420701