Hexan-3-yl acetate

Details

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Internal ID 7c158c6d-df25-4b04-8f43-0096facb282e
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Carboxylic acid esters
IUPAC Name hexan-3-yl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H16O2/c1-4-6-8(5-2)10-7(3)9/h8H,4-6H2,1-3H3
InChI Key RTIAQOLKVLAEAU-UHFFFAOYSA-N
Popularity 17 references in papers

Physical and Chemical Properties

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Molecular Formula C8H16O2
Molecular Weight 144.21 g/mol
Exact Mass 144.115029749 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.13
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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3-HEXYL ACETATE
40780-64-1
3-Hexanol, 3-acetate
Ethylbutylacetat
Hex-3-yl ethanoate
1-Ethylbutyl acetate
SCHEMBL282321
DTXSID70502041
Ethanol, 1,2-diethyl-, acetate
RTIAQOLKVLAEAU-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 Hexan-3-yl acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9951 99.51%
Caco-2 + 0.8981 89.81%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.4918 49.18%
OATP2B1 inhibitior - 0.8271 82.71%
OATP1B1 inhibitior + 0.9428 94.28%
OATP1B3 inhibitior + 0.9305 93.05%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9411 94.11%
P-glycoprotein inhibitior - 0.9745 97.45%
P-glycoprotein substrate - 0.9403 94.03%
CYP3A4 substrate - 0.6423 64.23%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8679 86.79%
CYP3A4 inhibition - 0.9540 95.40%
CYP2C9 inhibition - 0.9035 90.35%
CYP2C19 inhibition - 0.8984 89.84%
CYP2D6 inhibition - 0.9309 93.09%
CYP1A2 inhibition - 0.5078 50.78%
CYP2C8 inhibition - 0.9859 98.59%
CYP inhibitory promiscuity - 0.8235 82.35%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.6089 60.89%
Eye corrosion + 0.9639 96.39%
Eye irritation + 0.9151 91.51%
Skin irritation - 0.5352 53.52%
Skin corrosion - 0.9799 97.99%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6144 61.44%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5430 54.30%
skin sensitisation + 0.7850 78.50%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.6410 64.10%
Acute Oral Toxicity (c) III 0.9331 93.31%
Estrogen receptor binding - 0.9272 92.72%
Androgen receptor binding - 0.9167 91.67%
Thyroid receptor binding - 0.8798 87.98%
Glucocorticoid receptor binding - 0.9391 93.91%
Aromatase binding - 0.9130 91.30%
PPAR gamma - 0.9092 90.92%
Honey bee toxicity - 0.9393 93.93%
Biodegradation + 0.9000 90.00%
Crustacea aquatic toxicity - 0.7255 72.55%
Fish aquatic toxicity + 0.8049 80.49%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.48% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.85% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.93% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.76% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.99% 97.21%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.08% 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.
Elsholtzia fruticosa

Cross-Links

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PubChem 12545759
LOTUS LTS0191479
wikiData Q82354805