Methyl propionate

Details

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Internal ID 17fa2125-36f4-4bd5-82bf-1059f1eabba0
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Carboxylic acid esters > Methyl esters
IUPAC Name methyl propanoate
SMILES (Canonical) CCC(=O)OC
SMILES (Isomeric) CCC(=O)OC
InChI InChI=1S/C4H8O2/c1-3-4(5)6-2/h3H2,1-2H3
InChI Key RJUFJBKOKNCXHH-UHFFFAOYSA-N
Popularity 740 references in papers

Physical and Chemical Properties

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Molecular Formula C4H8O2
Molecular Weight 88.11 g/mol
Exact Mass 88.052429494 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.57
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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Methyl propanoate
554-12-1
Propanoic acid, methyl ester
Methyl propylate
Methylpropionate
Propionic acid, methyl ester
Propionate de methyle
PROPIONIC ACID METHYL ESTER
FEMA No. 2742
FEMA Number 2742
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 propionate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9964 99.64%
Caco-2 + 0.6721 67.21%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.6809 68.09%
OATP2B1 inhibitior - 0.8694 86.94%
OATP1B1 inhibitior + 0.9633 96.33%
OATP1B3 inhibitior + 0.9455 94.55%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9225 92.25%
P-glycoprotein inhibitior - 0.9856 98.56%
P-glycoprotein substrate - 0.9687 96.87%
CYP3A4 substrate - 0.7078 70.78%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8679 86.79%
CYP3A4 inhibition - 0.9875 98.75%
CYP2C9 inhibition - 0.9503 95.03%
CYP2C19 inhibition - 0.9525 95.25%
CYP2D6 inhibition - 0.9579 95.79%
CYP1A2 inhibition - 0.7906 79.06%
CYP2C8 inhibition - 0.9758 97.58%
CYP inhibitory promiscuity - 0.9346 93.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5874 58.74%
Carcinogenicity (trinary) Non-required 0.7204 72.04%
Eye corrosion + 0.9892 98.92%
Eye irritation + 0.9924 99.24%
Skin irritation + 0.8622 86.22%
Skin corrosion - 0.9060 90.60%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7609 76.09%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.7017 70.17%
skin sensitisation + 0.5821 58.21%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.4731 47.31%
Acute Oral Toxicity (c) IV 0.6358 63.58%
Estrogen receptor binding - 0.9515 95.15%
Androgen receptor binding - 0.9295 92.95%
Thyroid receptor binding - 0.9150 91.50%
Glucocorticoid receptor binding - 0.9126 91.26%
Aromatase binding - 0.8882 88.82%
PPAR gamma - 0.9091 90.91%
Honey bee toxicity - 0.9524 95.24%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity - 0.5737 57.37%

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 94.72% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.57% 96.95%
CHEMBL4040 P28482 MAP kinase ERK2 88.90% 83.82%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 84.70% 94.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.15% 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.
Actinidia chinensis
Ananas comosus
Coffea arabica
Ligusticum striatum
Panax notoginseng
Sinomenium acutum

Cross-Links

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PubChem 11124
NPASS NPC8187
LOTUS LTS0069440
wikiData Q418391