2-Hydroxyethyl propionate

Details

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Internal ID ce421f54-9d0b-43c4-8ae6-2fecae2c2ace
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Carboxylic acid esters
IUPAC Name 2-hydroxyethyl propanoate
SMILES (Canonical) CCC(=O)OCCO
SMILES (Isomeric) CCC(=O)OCCO
InChI InChI=1S/C5H10O3/c1-2-5(7)8-4-3-6/h6H,2-4H2,1H3
InChI Key SFAMKDPMPDEXGH-UHFFFAOYSA-N
Popularity 24 references in papers

Physical and Chemical Properties

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Molecular Formula C5H10O3
Molecular Weight 118.13 g/mol
Exact Mass 118.062994177 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 0.20
Atomic LogP (AlogP) -0.07
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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24567-27-9
2-hydroxyethyl propanoate
2-Hydroxyethyl propanaoate
1,2-Ethanediol, 1-propanoate
Propanoic acid, 2-hydroxyethyl ester
MFCD25961488
hydroxyethylpropionate
2-hydroxyethylpropionate
ethylene glycol monopropionate
SCHEMBL213301
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Hydroxyethyl propionate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9769 97.69%
Caco-2 + 0.8154 81.54%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.7296 72.96%
OATP2B1 inhibitior - 0.8480 84.80%
OATP1B1 inhibitior + 0.9338 93.38%
OATP1B3 inhibitior + 0.9301 93.01%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9178 91.78%
P-glycoprotein inhibitior - 0.9881 98.81%
P-glycoprotein substrate - 0.9717 97.17%
CYP3A4 substrate - 0.6467 64.67%
CYP2C9 substrate - 0.8120 81.20%
CYP2D6 substrate - 0.8669 86.69%
CYP3A4 inhibition - 0.9449 94.49%
CYP2C9 inhibition - 0.9232 92.32%
CYP2C19 inhibition - 0.9379 93.79%
CYP2D6 inhibition - 0.9506 95.06%
CYP1A2 inhibition - 0.8484 84.84%
CYP2C8 inhibition - 0.9332 93.32%
CYP inhibitory promiscuity - 0.9501 95.01%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.6839 68.39%
Eye corrosion + 0.9256 92.56%
Eye irritation + 0.9873 98.73%
Skin irritation - 0.5842 58.42%
Skin corrosion - 0.9374 93.74%
Ames mutagenesis - 0.8854 88.54%
Human Ether-a-go-go-Related Gene inhibition - 0.7479 74.79%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5834 58.34%
skin sensitisation - 0.8257 82.57%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.7016 70.16%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.5344 53.44%
Acute Oral Toxicity (c) III 0.5607 56.07%
Estrogen receptor binding - 0.9550 95.50%
Androgen receptor binding - 0.9101 91.01%
Thyroid receptor binding - 0.9268 92.68%
Glucocorticoid receptor binding - 0.8866 88.66%
Aromatase binding - 0.8823 88.23%
PPAR gamma - 0.8557 85.57%
Honey bee toxicity - 0.9664 96.64%
Biodegradation + 0.9500 95.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity - 0.6626 66.26%

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 95.48% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.43% 99.17%
CHEMBL4040 P28482 MAP kinase ERK2 83.87% 83.82%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.46% 96.95%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.31% 86.92%
CHEMBL2885 P07451 Carbonic anhydrase III 80.84% 87.45%

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.
Atractylodes lancea
Atractylodes macrocephala

Cross-Links

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PubChem 545098
NPASS NPC270266