Hex-3-enyl acetate

Details

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Internal ID 909520b4-56c2-4d50-b7bc-92c9261d7b80
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Carboxylic acid esters
IUPAC Name hex-3-enyl acetate
SMILES (Canonical) CCC=CCCOC(=O)C
SMILES (Isomeric) CCC=CCCOC(=O)C
InChI InChI=1S/C8H14O2/c1-3-4-5-6-7-10-8(2)9/h4-5H,3,6-7H2,1-2H3
InChI Key NPFVOOAXDOBMCE-UHFFFAOYSA-N
Popularity 134 references 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 1.90
Atomic LogP (AlogP) 1.91
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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3-Hexen-1-ol, acetate
1708-82-3
hex - 3 - enyl acetate
3-Hexen-1-ol, acetate, (3Z)-
3-hexen-1-ol acetate
DTXSID6047234
AKOS025243684
FT-0623908
FT-0623911
D88345

2D Structure

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2D Structure of Hex-3-enyl acetate

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 + 0.8105 81.05%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.4663 46.63%
OATP2B1 inhibitior - 0.8495 84.95%
OATP1B1 inhibitior + 0.8949 89.49%
OATP1B3 inhibitior + 0.9152 91.52%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8397 83.97%
P-glycoprotein inhibitior - 0.9903 99.03%
P-glycoprotein substrate - 0.9804 98.04%
CYP3A4 substrate - 0.6391 63.91%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8696 86.96%
CYP3A4 inhibition - 0.9462 94.62%
CYP2C9 inhibition - 0.9397 93.97%
CYP2C19 inhibition - 0.9493 94.93%
CYP2D6 inhibition - 0.9247 92.47%
CYP1A2 inhibition + 0.5293 52.93%
CYP2C8 inhibition - 0.9610 96.10%
CYP inhibitory promiscuity - 0.7344 73.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6400 64.00%
Carcinogenicity (trinary) Non-required 0.7106 71.06%
Eye corrosion + 0.9586 95.86%
Eye irritation + 0.9798 97.98%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9963 99.63%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5787 57.87%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation + 0.7904 79.04%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.5557 55.57%
Acute Oral Toxicity (c) III 0.8757 87.57%
Estrogen receptor binding - 0.9255 92.55%
Androgen receptor binding - 0.8110 81.10%
Thyroid receptor binding - 0.9203 92.03%
Glucocorticoid receptor binding - 0.8184 81.84%
Aromatase binding - 0.8953 89.53%
PPAR gamma - 0.7167 71.67%
Honey bee toxicity - 0.9399 93.99%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.9505 95.05%

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 93.27% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.44% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.36% 96.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.82% 97.25%
CHEMBL2581 P07339 Cathepsin D 81.56% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.00% 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.
Daucus carota
Fragaria × ananassa
Malus sylvestris
Medicago sativa
Micromeria sinaica
Quercus agrifolia
Rhanterium epapposum

Cross-Links

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PubChem 15574
NPASS NPC155009
LOTUS LTS0086272
wikiData Q81984400