Butyl propionate

Details

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Internal ID 4c6ecff9-0746-404e-851c-05c1a28f4f9e
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Carboxylic acid esters
IUPAC Name butyl propanoate
SMILES (Canonical) CCCCOC(=O)CC
SMILES (Isomeric) CCCCOC(=O)CC
InChI InChI=1S/C7H14O2/c1-3-5-6-9-7(8)4-2/h3-6H2,1-2H3
InChI Key BTMVHUNTONAYDX-UHFFFAOYSA-N
Popularity 215 references in papers

Physical and Chemical Properties

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Molecular Formula C7H14O2
Molecular Weight 130.18 g/mol
Exact Mass 130.099379685 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.74
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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590-01-2
Butyl propanoate
N-BUTYL PROPIONATE
Propanoic acid, butyl ester
Propionic Acid Butyl Ester
Butyl propionate (natural)
n-Butyl n-propionate
n-butylpropionate
UNII-2NXC4AK99E
EINECS 209-669-5
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Butyl propionate

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 + 0.9462 94.62%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.6090 60.90%
OATP2B1 inhibitior - 0.8416 84.16%
OATP1B1 inhibitior + 0.9361 93.61%
OATP1B3 inhibitior + 0.9171 91.71%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8889 88.89%
P-glycoprotein inhibitior - 0.9870 98.70%
P-glycoprotein substrate - 0.9624 96.24%
CYP3A4 substrate - 0.5917 59.17%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8679 86.79%
CYP3A4 inhibition - 0.9513 95.13%
CYP2C9 inhibition - 0.9277 92.77%
CYP2C19 inhibition - 0.9391 93.91%
CYP2D6 inhibition - 0.9225 92.25%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.8730 87.30%
CYP inhibitory promiscuity - 0.8517 85.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6400 64.00%
Carcinogenicity (trinary) Non-required 0.6625 66.25%
Eye corrosion + 0.9870 98.70%
Eye irritation + 0.9828 98.28%
Skin irritation - 0.6447 64.47%
Skin corrosion - 0.9941 99.41%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6719 67.19%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation + 0.7184 71.84%
Respiratory toxicity - 0.9000 90.00%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.6240 62.40%
Acute Oral Toxicity (c) III 0.8356 83.56%
Estrogen receptor binding - 0.9567 95.67%
Androgen receptor binding - 0.8679 86.79%
Thyroid receptor binding - 0.9112 91.12%
Glucocorticoid receptor binding - 0.9404 94.04%
Aromatase binding - 0.9286 92.86%
PPAR gamma - 0.8954 89.54%
Honey bee toxicity - 0.9914 99.14%
Biodegradation + 0.9750 97.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9484 94.84%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.96% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.77% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.99% 96.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.80% 97.25%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 85.70% 97.29%
CHEMBL2581 P07339 Cathepsin D 85.56% 98.95%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 84.57% 80.78%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.76% 97.21%
CHEMBL221 P23219 Cyclooxygenase-1 80.36% 90.17%

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.
Elsholtzia ciliata
Mosla chinensis
Prunus armeniaca

Cross-Links

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PubChem 11529
NPASS NPC166804
LOTUS LTS0210550
wikiData Q2726127