Ethyl 2-heptenoate

Details

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Internal ID d7c20cd6-c8b1-4f75-bb75-32991d149d88
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name ethyl (E)-hept-2-enoate
SMILES (Canonical) CCCCC=CC(=O)OCC
SMILES (Isomeric) CCCC/C=C/C(=O)OCC
InChI InChI=1S/C9H16O2/c1-3-5-6-7-8-9(10)11-4-2/h7-8H,3-6H2,1-2H3/b8-7+
InChI Key CYLQPOIZDBIXFP-BQYQJAHWSA-N
Popularity 14 references in papers

Physical and Chemical Properties

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Molecular Formula C9H16O2
Molecular Weight 156.22 g/mol
Exact Mass 156.115029749 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.30
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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ethyl hept-2-enoate
54340-72-6
Ethyl 2-heptenoate
XYH9LG7DSY
Ethyl (E)-2-heptenoate
UNII-XYH9LG7DSY
ethyl trans-2-heptenoate
(E)-2-Ethyl heptenoate
2-Heptenoic acid, ethyl ester, (E)-
NSC 244958
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 2-heptenoate

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 + 0.9569 95.69%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.4854 48.54%
OATP2B1 inhibitior - 0.8568 85.68%
OATP1B1 inhibitior + 0.8880 88.80%
OATP1B3 inhibitior + 0.9245 92.45%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7992 79.92%
P-glycoprotein inhibitior - 0.9852 98.52%
P-glycoprotein substrate - 0.9810 98.10%
CYP3A4 substrate - 0.5567 55.67%
CYP2C9 substrate + 0.6104 61.04%
CYP2D6 substrate - 0.9019 90.19%
CYP3A4 inhibition - 0.9692 96.92%
CYP2C9 inhibition - 0.9225 92.25%
CYP2C19 inhibition - 0.8783 87.83%
CYP2D6 inhibition - 0.9374 93.74%
CYP1A2 inhibition + 0.5261 52.61%
CYP2C8 inhibition - 0.8987 89.87%
CYP inhibitory promiscuity - 0.7753 77.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5400 54.00%
Carcinogenicity (trinary) Non-required 0.5937 59.37%
Eye corrosion + 0.9724 97.24%
Eye irritation + 0.9807 98.07%
Skin irritation + 0.9245 92.45%
Skin corrosion - 0.7863 78.63%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7688 76.88%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5199 51.99%
skin sensitisation + 0.9350 93.50%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.6754 67.54%
Acute Oral Toxicity (c) III 0.8023 80.23%
Estrogen receptor binding - 0.8705 87.05%
Androgen receptor binding - 0.8120 81.20%
Thyroid receptor binding - 0.8371 83.71%
Glucocorticoid receptor binding - 0.7251 72.51%
Aromatase binding - 0.8588 85.88%
PPAR gamma - 0.7682 76.82%
Honey bee toxicity - 0.9820 98.20%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9234 92.34%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 93.60% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 91.53% 96.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.48% 96.09%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 86.50% 97.21%
CHEMBL2581 P07339 Cathepsin D 84.20% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 83.86% 94.73%
CHEMBL2664 P23526 Adenosylhomocysteinase 82.73% 86.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.54% 86.33%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.89% 93.56%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.29% 94.33%

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.
Scorzonera laciniata

Cross-Links

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PubChem 5358363
LOTUS LTS0225721
wikiData Q76305037