Ethyl sorbate

Details

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Internal ID 37550489-a86e-43c4-8267-d50192116db9
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name ethyl (2E,4E)-hexa-2,4-dienoate
SMILES (Canonical) CCOC(=O)C=CC=CC
SMILES (Isomeric) CCOC(=O)/C=C/C=C/C
InChI InChI=1S/C8H12O2/c1-3-5-6-7-8(9)10-4-2/h3,5-7H,4H2,1-2H3/b5-3+,7-6+
InChI Key OZZYKXXGCOLLLO-TWTPFVCWSA-N
Popularity 68 references in papers

Physical and Chemical Properties

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Molecular Formula C8H12O2
Molecular Weight 140.18 g/mol
Exact Mass 140.083729621 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.68
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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2396-84-1
Ethyl hexa-2,4-dienoate
Ethyl 2,4-hexadienoate
Sorbic acid, ethyl ester
2,4-Hexadienoic acid, ethyl ester
ethyl (2E,4E)-hexa-2,4-dienoate
2,4-Hexadienoic acid, ethyl ester, (2E,4E)-
FEMA No. 2459
Sorbic Acid Ethyl Ester
Ethyl (E,E)-2,4-hexadienoate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Ethyl sorbate

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 + 0.8894 88.94%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.6570 65.70%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9293 92.93%
OATP1B3 inhibitior + 0.9571 95.71%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8428 84.28%
P-glycoprotein inhibitior - 0.9930 99.30%
P-glycoprotein substrate - 0.9893 98.93%
CYP3A4 substrate - 0.6003 60.03%
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 - 0.9208 92.08%
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 + 0.9938 99.38%
Skin irritation + 0.9358 93.58%
Skin corrosion - 0.6906 69.06%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6907 69.07%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5149 51.49%
skin sensitisation + 0.8587 85.87%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.8111 81.11%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.5458 54.58%
Acute Oral Toxicity (c) III 0.8792 87.92%
Estrogen receptor binding - 0.9123 91.23%
Androgen receptor binding - 0.8537 85.37%
Thyroid receptor binding - 0.8984 89.84%
Glucocorticoid receptor binding - 0.8716 87.16%
Aromatase binding - 0.9055 90.55%
PPAR gamma - 0.9049 90.49%
Honey bee toxicity - 0.9393 93.93%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.7455 74.55%
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
CHEMBL4040 P28482 MAP kinase ERK2 98.39% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.27% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.27% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 85.61% 94.73%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.03% 97.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.57% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 81.36% 90.17%

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.
Averrhoa carambola

Cross-Links

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PubChem 1550470
LOTUS LTS0045485
wikiData Q63398535