Methyl 4-heptenoate

Details

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Internal ID e2a86476-b479-4329-b7c3-c3f4f1ae7c72
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters > Fatty acid methyl esters
IUPAC Name methyl hept-4-enoate
SMILES (Canonical) CCC=CCCC(=O)OC
SMILES (Isomeric) CCC=CCCC(=O)OC
InChI InChI=1S/C8H14O2/c1-3-4-5-6-7-8(9)10-2/h4-5H,3,6-7H2,1-2H3
InChI Key CVDVXDORDMZHRW-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C8H14O2
Molecular Weight 142.20 g/mol
Exact Mass 142.099379685 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.91
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 4-heptenoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9962 99.62%
Caco-2 + 0.7576 75.76%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Plasma membrane 0.5877 58.77%
OATP2B1 inhibitior - 0.8538 85.38%
OATP1B1 inhibitior + 0.8683 86.83%
OATP1B3 inhibitior + 0.8879 88.79%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8558 85.58%
P-glycoprotein inhibitior - 0.9882 98.82%
P-glycoprotein substrate - 0.9619 96.19%
CYP3A4 substrate - 0.6504 65.04%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8696 86.96%
CYP3A4 inhibition - 0.9738 97.38%
CYP2C9 inhibition - 0.9432 94.32%
CYP2C19 inhibition - 0.9521 95.21%
CYP2D6 inhibition - 0.9519 95.19%
CYP1A2 inhibition - 0.5574 55.74%
CYP2C8 inhibition - 0.9585 95.85%
CYP inhibitory promiscuity - 0.8346 83.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.7586 75.86%
Eye corrosion + 0.9418 94.18%
Eye irritation + 0.9688 96.88%
Skin irritation + 0.5097 50.97%
Skin corrosion - 0.9951 99.51%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6910 69.10%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.7940 79.40%
skin sensitisation + 0.8003 80.03%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity - 0.6023 60.23%
Acute Oral Toxicity (c) III 0.7281 72.81%
Estrogen receptor binding - 0.9713 97.13%
Androgen receptor binding - 0.9262 92.62%
Thyroid receptor binding - 0.8882 88.82%
Glucocorticoid receptor binding - 0.8232 82.32%
Aromatase binding - 0.9219 92.19%
PPAR gamma - 0.7927 79.27%
Honey bee toxicity - 0.9445 94.45%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9123 91.23%

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 93.72% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.12% 96.09%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 86.06% 94.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.13% 96.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.75% 89.34%

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.
Nicotiana tabacum

Cross-Links

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PubChem 535039
LOTUS LTS0009023
wikiData Q104970684