cis-3-Hexenyl acetate

Details

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Internal ID 3078c6f3-9b6f-43b2-a2ff-039e21f6e9c8
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Carboxylic acid esters
IUPAC Name [(Z)-hex-3-enyl] acetate
SMILES (Canonical) CCC=CCCOC(=O)C
SMILES (Isomeric) CC/C=C\CCOC(=O)C
InChI InChI=1S/C8H14O2/c1-3-4-5-6-7-10-8(2)9/h4-5H,3,6-7H2,1-2H3/b5-4-
InChI Key NPFVOOAXDOBMCE-PLNGDYQASA-N
Popularity 693 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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3681-71-8
(Z)-3-HEXENYL ACETATE
[(Z)-hex-3-enyl] acetate
Leaf acetate
(Z)-Hex-3-enyl acetate
3-Hexenylacetate
cis-3-Hexen-1-yl acetate
3-Hexen-1-ol, acetate, (Z)-
cis-3-Hexenyl ethanoate
(3Z)-3-Hexenyl acetate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of cis-3-Hexenyl 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.
Artemisia argyi
Artemisia montana
Artemisia princeps
Artemisia scoparia
Crataegus pinnatifida
Daucus carota
Lonicera japonica
Medicago sativa
Olea europaea
Persicaria bistorta
Pterocarpus indicus
Quercus agrifolia

Cross-Links

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PubChem 5363388
NPASS NPC226511
LOTUS LTS0167261
wikiData Q1368869