Hex-1-en-1-yl pentanoate

Details

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Internal ID a56d2b14-05a2-4e27-b86b-cb39458032be
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name hex-1-enyl pentanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H20O2/c1-3-5-7-8-10-13-11(12)9-6-4-2/h8,10H,3-7,9H2,1-2H3
InChI Key QVSWHXAMEIASBU-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C11H20O2
Molecular Weight 184.27 g/mol
Exact Mass 184.146329876 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.42
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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HEX-1-EN-1-YL PENTANOATE
84818-96-2
DTXSID00827370

2D Structure

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2D Structure of Hex-1-en-1-yl pentanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 + 0.9348 93.48%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Plasma membrane 0.6046 60.46%
OATP2B1 inhibitior - 0.8482 84.82%
OATP1B1 inhibitior + 0.7429 74.29%
OATP1B3 inhibitior + 0.9059 90.59%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7305 73.05%
P-glycoprotein inhibitior - 0.9763 97.63%
P-glycoprotein substrate - 0.9382 93.82%
CYP3A4 substrate - 0.6241 62.41%
CYP2C9 substrate - 0.7980 79.80%
CYP2D6 substrate - 0.8654 86.54%
CYP3A4 inhibition - 0.9576 95.76%
CYP2C9 inhibition - 0.9329 93.29%
CYP2C19 inhibition - 0.8926 89.26%
CYP2D6 inhibition - 0.9487 94.87%
CYP1A2 inhibition + 0.5599 55.99%
CYP2C8 inhibition - 0.8498 84.98%
CYP inhibitory promiscuity - 0.8284 82.84%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5200 52.00%
Carcinogenicity (trinary) Non-required 0.6304 63.04%
Eye corrosion + 0.9850 98.50%
Eye irritation + 0.9350 93.50%
Skin irritation + 0.8296 82.96%
Skin corrosion - 0.6055 60.55%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6262 62.62%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5649 56.49%
skin sensitisation + 0.9248 92.48%
Respiratory toxicity - 0.9222 92.22%
Reproductive toxicity - 0.8889 88.89%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity - 0.5657 56.57%
Acute Oral Toxicity (c) III 0.7045 70.45%
Estrogen receptor binding - 0.7416 74.16%
Androgen receptor binding - 0.8577 85.77%
Thyroid receptor binding - 0.8122 81.22%
Glucocorticoid receptor binding - 0.7732 77.32%
Aromatase binding - 0.8175 81.75%
PPAR gamma - 0.6803 68.03%
Honey bee toxicity - 0.9842 98.42%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.8712 87.12%

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 95.47% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.94% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.21% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 90.72% 96.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.11% 86.33%
CHEMBL1974 P36888 Tyrosine-protein kinase receptor FLT3 81.92% 91.83%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.78% 94.33%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.29% 92.08%

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.
Nepeta nepetella

Cross-Links

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PubChem 71406771
LOTUS LTS0125066
wikiData Q82811753