Isobutyl propionate

Details

Top
Internal ID 6c647d2a-4332-4d7d-84fe-5cd73ba5d144
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Carboxylic acid esters
IUPAC Name 2-methylpropyl propanoate
SMILES (Canonical) CCC(=O)OCC(C)C
SMILES (Isomeric) CCC(=O)OCC(C)C
InChI InChI=1S/C7H14O2/c1-4-7(8)9-5-6(2)3/h6H,4-5H2,1-3H3
InChI Key FZXRXKLUIMKDEL-UHFFFAOYSA-N
Popularity 56 references in papers

Physical and Chemical Properties

Top
Molecular Formula C7H14O2
Molecular Weight 130.18 g/mol
Exact Mass 130.099379685 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.20
Atomic LogP (AlogP) 1.60
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

Top
540-42-1
Isobutyl propanoate
2-METHYLPROPYL PROPANOATE
Propanoic acid, 2-methylpropyl ester
Propionic Acid Isobutyl Ester
2-Methylpropyl propionate
Propionic acid, isobutyl ester
Methyl isobutyl acetate
2-Methyl-1-propyl propanoate
FEMA No. 2212
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Isobutyl propionate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.7787 77.87%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7148 71.48%
OATP2B1 inhibitior - 0.8379 83.79%
OATP1B1 inhibitior + 0.9498 94.98%
OATP1B3 inhibitior + 0.9413 94.13%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8570 85.70%
P-glycoprotein inhibitior - 0.9734 97.34%
P-glycoprotein substrate - 0.9667 96.67%
CYP3A4 substrate - 0.6723 67.23%
CYP2C9 substrate + 0.5942 59.42%
CYP2D6 substrate - 0.8718 87.18%
CYP3A4 inhibition - 0.9569 95.69%
CYP2C9 inhibition - 0.9157 91.57%
CYP2C19 inhibition - 0.9333 93.33%
CYP2D6 inhibition - 0.9388 93.88%
CYP1A2 inhibition - 0.7339 73.39%
CYP2C8 inhibition - 0.9880 98.80%
CYP inhibitory promiscuity - 0.8492 84.92%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5600 56.00%
Carcinogenicity (trinary) Warning 0.5386 53.86%
Eye corrosion + 0.9748 97.48%
Eye irritation + 0.9864 98.64%
Skin irritation - 0.6793 67.93%
Skin corrosion - 0.9856 98.56%
Ames mutagenesis - 0.9600 96.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7062 70.62%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation + 0.7223 72.23%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity - 0.6981 69.81%
Acute Oral Toxicity (c) III 0.8141 81.41%
Estrogen receptor binding - 0.9682 96.82%
Androgen receptor binding - 0.9223 92.23%
Thyroid receptor binding - 0.9255 92.55%
Glucocorticoid receptor binding - 0.9331 93.31%
Aromatase binding - 0.8907 89.07%
PPAR gamma - 0.9237 92.37%
Honey bee toxicity - 0.9530 95.30%
Biodegradation + 0.8750 87.50%
Crustacea aquatic toxicity - 0.7255 72.55%
Fish aquatic toxicity + 0.8741 87.41%

Targets

Top

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 95.14% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.84% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.77% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.13% 99.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.54% 97.25%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.90% 100.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.75% 96.47%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.44% 97.21%

Plants that contains it

Top
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.
Humulus lupulus

Cross-Links

Top
PubChem 10895
NPASS NPC3560
LOTUS LTS0049923
wikiData Q27160785