2-Hydroxyethyl acrylate

Details

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Internal ID f94154d3-5e88-49f6-a32a-8fa3ecdf7035
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Acrylic acids and derivatives > Acrylic acid esters
IUPAC Name 2-hydroxyethyl prop-2-enoate
SMILES (Canonical) C=CC(=O)OCCO
SMILES (Isomeric) C=CC(=O)OCCO
InChI InChI=1S/C5H8O3/c1-2-5(7)8-4-3-6/h2,6H,1,3-4H2
InChI Key OMIGHNLMNHATMP-UHFFFAOYSA-N
Popularity 669 references in papers

Physical and Chemical Properties

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Molecular Formula C5H8O3
Molecular Weight 116.11 g/mol
Exact Mass 116.047344113 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP -0.20
Atomic LogP (AlogP) -0.29
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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818-61-1
Hydroxyethyl acrylate
2-Propenoic acid, 2-hydroxyethyl ester
Ethylene glycol monoacrylate
Bisomer 2HEA
2-(Acryloyloxy)ethanol
Ethylene glycol, acrylate
Acrylic acid, 2-hydroxyethyl ester
Ethylene glycol, monoacrylate
DTXSID2022123
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 acrylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9489 94.89%
Caco-2 + 0.9009 90.09%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.6998 69.98%
OATP2B1 inhibitior - 0.8562 85.62%
OATP1B1 inhibitior + 0.9427 94.27%
OATP1B3 inhibitior + 0.9492 94.92%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9411 94.11%
P-glycoprotein inhibitior - 0.9880 98.80%
P-glycoprotein substrate - 0.9902 99.02%
CYP3A4 substrate - 0.6612 66.12%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8769 87.69%
CYP3A4 inhibition - 0.8983 89.83%
CYP2C9 inhibition - 0.9405 94.05%
CYP2C19 inhibition - 0.9168 91.68%
CYP2D6 inhibition - 0.9601 96.01%
CYP1A2 inhibition - 0.8671 86.71%
CYP2C8 inhibition - 0.9538 95.38%
CYP inhibitory promiscuity - 0.9593 95.93%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Non-required 0.7103 71.03%
Eye corrosion + 0.9875 98.75%
Eye irritation + 0.9831 98.31%
Skin irritation + 0.7315 73.15%
Skin corrosion + 0.7832 78.32%
Ames mutagenesis - 0.9554 95.54%
Human Ether-a-go-go-Related Gene inhibition - 0.7936 79.36%
Micronuclear - 0.9768 97.68%
Hepatotoxicity + 0.5053 50.53%
skin sensitisation + 0.9334 93.34%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.6529 65.29%
Acute Oral Toxicity (c) III 0.8038 80.38%
Estrogen receptor binding - 0.8719 87.19%
Androgen receptor binding - 0.5391 53.91%
Thyroid receptor binding - 0.8908 89.08%
Glucocorticoid receptor binding - 0.6677 66.77%
Aromatase binding - 0.8260 82.60%
PPAR gamma - 0.7183 71.83%
Honey bee toxicity - 0.8084 80.84%
Biodegradation + 0.9500 95.00%
Crustacea aquatic toxicity - 0.9100 91.00%
Fish aquatic toxicity - 0.7721 77.21%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL1963 P16473 Thyroid stimulating hormone receptor 7943.3 nM
7943.3 nM
Potency
Potency
via CMAUP
via CMAUP

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4040 P28482 MAP kinase ERK2 88.32% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.41% 96.09%
CHEMBL3587 Q02750 Dual specificity mitogen-activated protein kinase kinase 1 86.08% 97.93%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.75% 99.17%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 83.76% 82.05%
CHEMBL2885 P07451 Carbonic anhydrase III 82.14% 87.45%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.03% 86.92%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.26% 96.95%

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.
Angelica dahurica

Cross-Links

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PubChem 13165
NPASS NPC203382
ChEMBL CHEMBL1330518