Acrylic acid

Details

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Internal ID dd832c2f-7f1e-4ab1-aadb-cce3d6451acb
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Acrylic acids and derivatives > Acrylic acids
IUPAC Name prop-2-enoic acid
SMILES (Canonical) C=CC(=O)O
SMILES (Isomeric) C=CC(=O)O
InChI InChI=1S/C3H4O2/c1-2-3(4)5/h2H,1H2,(H,4,5)
InChI Key NIXOWILDQLNWCW-UHFFFAOYSA-N
Popularity 13,574 references in papers

Physical and Chemical Properties

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Molecular Formula C3H4O2
Molecular Weight 72.06 g/mol
Exact Mass 72.021129366 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 0.30
Atomic LogP (AlogP) 0.26
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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2-Propenoic acid
79-10-7
prop-2-enoic acid
Vinylformic acid
Propenoic acid
Acroleic acid
Ethylenecarboxylic acid
Propene acid
ACRYLATE
Propenoate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Acrylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9913 99.13%
Caco-2 + 0.8494 84.94%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Plasma membrane 0.4376 43.76%
OATP2B1 inhibitior - 0.8678 86.78%
OATP1B1 inhibitior + 0.9664 96.64%
OATP1B3 inhibitior + 0.9516 95.16%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9617 96.17%
P-glycoprotein inhibitior - 0.9886 98.86%
P-glycoprotein substrate - 0.9985 99.85%
CYP3A4 substrate - 0.8188 81.88%
CYP2C9 substrate - 0.6031 60.31%
CYP2D6 substrate - 0.8917 89.17%
CYP3A4 inhibition - 0.9391 93.91%
CYP2C9 inhibition - 0.9576 95.76%
CYP2C19 inhibition - 0.9637 96.37%
CYP2D6 inhibition - 0.9634 96.34%
CYP1A2 inhibition - 0.9195 91.95%
CYP2C8 inhibition - 0.9914 99.14%
CYP inhibitory promiscuity - 0.9849 98.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.7322 73.22%
Carcinogenicity (trinary) Non-required 0.7289 72.89%
Eye corrosion + 1.0000 100.00%
Eye irritation + 0.9756 97.56%
Skin irritation + 0.9538 95.38%
Skin corrosion + 0.9679 96.79%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8535 85.35%
Micronuclear - 0.6900 69.00%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation + 0.8602 86.02%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.6490 64.90%
Acute Oral Toxicity (c) I 0.7161 71.61%
Estrogen receptor binding - 0.8860 88.60%
Androgen receptor binding - 0.8951 89.51%
Thyroid receptor binding - 0.8737 87.37%
Glucocorticoid receptor binding - 0.8743 87.43%
Aromatase binding - 0.9128 91.28%
PPAR gamma - 0.7925 79.25%
Honey bee toxicity - 0.8126 81.26%
Biodegradation + 0.9000 90.00%
Crustacea aquatic toxicity - 0.9400 94.00%
Fish aquatic toxicity + 0.7734 77.34%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL1293235 P02545 Prelamin-A/C 35481.3 nM
Potency
via CMAUP

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 92.11% 82.05%
CHEMBL4040 P28482 MAP kinase ERK2 85.45% 83.82%
CHEMBL5251 Q06187 Tyrosine-protein kinase BTK 83.34% 98.51%
CHEMBL340 P08684 Cytochrome P450 3A4 81.68% 91.19%

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.
Eschweilera coriacea
Eucalyptus cladocalyx
Peltodon longipes
Salvadora persica
Vitis vinifera

Cross-Links

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PubChem 6581
NPASS NPC20903
ChEMBL CHEMBL1213529