Ethyl 3-acetoxyhexanoate

Details

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Internal ID d2e02d1e-9c36-4884-a4fd-ae5c00ba4bfb
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name ethyl 3-acetyloxyhexanoate
SMILES (Canonical) CCCC(CC(=O)OCC)OC(=O)C
SMILES (Isomeric) CCCC(CC(=O)OCC)OC(=O)C
InChI InChI=1S/C10H18O4/c1-4-6-9(14-8(3)11)7-10(12)13-5-2/h9H,4-7H2,1-3H3
InChI Key UYBMIHNGXIOMAW-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O4
Molecular Weight 202.25 g/mol
Exact Mass 202.12050905 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.67
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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21188-61-4
ethyl 3-acetyloxyhexanoate
Hexanoic acid, 3-(acetyloxy)-, ethyl ester
Ethyl 3 Acetoxy Hexanoate
Ethyl 3-acetoxy hexanoate
3-Acetoxyhexanoic Acid Ethyl Ester
SCHEMBL8862332
DTXSID30275860
DTXSID40864981
UYBMIHNGXIOMAW-UHFFFAOYSA-N
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 3-acetoxyhexanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9686 96.86%
Caco-2 + 0.8415 84.15%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8503 85.03%
OATP2B1 inhibitior - 0.8425 84.25%
OATP1B1 inhibitior + 0.9501 95.01%
OATP1B3 inhibitior + 0.9611 96.11%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9314 93.14%
P-glycoprotein inhibitior - 0.9611 96.11%
P-glycoprotein substrate - 0.9516 95.16%
CYP3A4 substrate - 0.5362 53.62%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8679 86.79%
CYP3A4 inhibition - 0.8348 83.48%
CYP2C9 inhibition - 0.8511 85.11%
CYP2C19 inhibition - 0.8511 85.11%
CYP2D6 inhibition - 0.9213 92.13%
CYP1A2 inhibition - 0.8341 83.41%
CYP2C8 inhibition - 0.9549 95.49%
CYP inhibitory promiscuity - 0.7731 77.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5966 59.66%
Carcinogenicity (trinary) Non-required 0.5306 53.06%
Eye corrosion + 0.6448 64.48%
Eye irritation + 0.9513 95.13%
Skin irritation - 0.8271 82.71%
Skin corrosion - 0.9720 97.20%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6569 65.69%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5032 50.32%
skin sensitisation - 0.9040 90.40%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.7898 78.98%
Acute Oral Toxicity (c) III 0.6810 68.10%
Estrogen receptor binding - 0.7117 71.17%
Androgen receptor binding - 0.9093 90.93%
Thyroid receptor binding - 0.8387 83.87%
Glucocorticoid receptor binding - 0.8210 82.10%
Aromatase binding - 0.8120 81.20%
PPAR gamma - 0.8943 89.43%
Honey bee toxicity - 0.8915 89.15%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.5155 51.55%
Fish aquatic toxicity + 0.8440 84.40%

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
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 95.76% 97.21%
CHEMBL4040 P28482 MAP kinase ERK2 94.99% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.76% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.63% 96.95%
CHEMBL2581 P07339 Cathepsin D 88.08% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.84% 99.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.01% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 81.65% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.26% 94.45%

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.
Ananas comosus

Cross-Links

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PubChem 89464
LOTUS LTS0016571
wikiData Q72472167