2-Butenoic acid, ethyl ester

Details

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Internal ID bd3a7606-1dc5-41ff-a278-62eed06cdb22
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name ethyl but-2-enoate
SMILES (Canonical) CCOC(=O)C=CC
SMILES (Isomeric) CCOC(=O)C=CC
InChI InChI=1S/C6H10O2/c1-3-5-6(7)8-4-2/h3,5H,4H2,1-2H3
InChI Key ZFDIRQKJPRINOQ-UHFFFAOYSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C6H10O2
Molecular Weight 114.14 g/mol
Exact Mass 114.068079557 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.13
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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2-Butenoic acid, ethyl ester
but-2-enoic acid ethyl ester
ethyl butenoate
Ethyl-2-Crotonate
DTXSID8065119
AKOS025243553
FT-0625771
FT-0626173
FT-0642600
FT-0686368

2D Structure

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2D Structure of 2-Butenoic acid, ethyl ester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8690 86.90%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6570 65.70%
OATP2B1 inhibitior - 0.8654 86.54%
OATP1B1 inhibitior + 0.9416 94.16%
OATP1B3 inhibitior + 0.9571 95.71%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8834 88.34%
P-glycoprotein inhibitior - 0.9914 99.14%
P-glycoprotein substrate - 0.9941 99.41%
CYP3A4 substrate - 0.6396 63.96%
CYP2C9 substrate + 0.5936 59.36%
CYP2D6 substrate - 0.9103 91.03%
CYP3A4 inhibition - 0.9716 97.16%
CYP2C9 inhibition - 0.9342 93.42%
CYP2C19 inhibition - 0.9406 94.06%
CYP2D6 inhibition - 0.9547 95.47%
CYP1A2 inhibition - 0.6777 67.77%
CYP2C8 inhibition - 0.9471 94.71%
CYP inhibitory promiscuity - 0.7520 75.20%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5874 58.74%
Carcinogenicity (trinary) Non-required 0.5961 59.61%
Eye corrosion + 0.9743 97.43%
Eye irritation + 0.9946 99.46%
Skin irritation + 0.9358 93.58%
Skin corrosion - 0.6906 69.06%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7806 78.06%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5774 57.74%
skin sensitisation + 0.8587 85.87%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.8111 81.11%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.6069 60.69%
Acute Oral Toxicity (c) III 0.8792 87.92%
Estrogen receptor binding - 0.9406 94.06%
Androgen receptor binding - 0.9020 90.20%
Thyroid receptor binding - 0.8785 87.85%
Glucocorticoid receptor binding - 0.8596 85.96%
Aromatase binding - 0.8726 87.26%
PPAR gamma - 0.9383 93.83%
Honey bee toxicity - 0.9266 92.66%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.7955 79.55%
Fish aquatic toxicity + 0.7920 79.20%

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 91.18% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.86% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 86.86% 97.21%
CHEMBL4040 P28482 MAP kinase ERK2 86.46% 83.82%
CHEMBL3401 O75469 Pregnane X receptor 86.10% 94.73%
CHEMBL2664 P23526 Adenosylhomocysteinase 84.08% 86.67%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.57% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.02% 86.33%

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.
Dactylanthus taylorii
Mangifera indica

Cross-Links

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PubChem 12191
LOTUS LTS0246059
wikiData Q81991999