cis-3-Hexenyl phenylacetate

Details

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Internal ID 57845d9d-838c-448c-a598-623bb9c2f535
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name [(Z)-hex-3-enyl] 2-phenylacetate
SMILES (Canonical) CCC=CCCOC(=O)CC1=CC=CC=C1
SMILES (Isomeric) CC/C=C\CCOC(=O)CC1=CC=CC=C1
InChI InChI=1S/C14H18O2/c1-2-3-4-8-11-16-14(15)12-13-9-6-5-7-10-13/h3-7,9-10H,2,8,11-12H2,1H3/b4-3-
InChI Key FJKFIIYSBXHBCT-ARJAWSKDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H18O2
Molecular Weight 218.29 g/mol
Exact Mass 218.130679813 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.13
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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42436-07-7
Z-3-Hexenyl phenylacetate
3-Hexenyl phenylacetate, cis-
FEMA No. 3633
3-Hexenyl phenylacetate
3-Hexenyl alpha-toluate
Benzeneacetic acid, (3Z)-3-hexenyl ester
Benzeneacetic acid, 3-hexenyl ester, (Z)-
(3Z)-3-Hexenyl phenylacetate
(Z)-Hex-3-enyl phenylacetate
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 phenylacetate

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 + 0.8437 84.37%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Plasma membrane 0.6423 64.23%
OATP2B1 inhibitior - 0.8636 86.36%
OATP1B1 inhibitior + 0.8463 84.63%
OATP1B3 inhibitior + 0.9394 93.94%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.6301 63.01%
P-glycoprotein inhibitior - 0.9721 97.21%
P-glycoprotein substrate - 0.9617 96.17%
CYP3A4 substrate - 0.6025 60.25%
CYP2C9 substrate - 0.6063 60.63%
CYP2D6 substrate - 0.8427 84.27%
CYP3A4 inhibition - 0.9372 93.72%
CYP2C9 inhibition - 0.8750 87.50%
CYP2C19 inhibition - 0.8059 80.59%
CYP2D6 inhibition - 0.8910 89.10%
CYP1A2 inhibition + 0.6202 62.02%
CYP2C8 inhibition - 0.6126 61.26%
CYP inhibitory promiscuity + 0.5320 53.20%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.5923 59.23%
Eye corrosion + 0.5768 57.68%
Eye irritation + 0.9623 96.23%
Skin irritation - 0.6643 66.43%
Skin corrosion - 0.9979 99.79%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3820 38.20%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation + 0.7692 76.92%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.8585 85.85%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity - 0.7877 78.77%
Acute Oral Toxicity (c) III 0.9144 91.44%
Estrogen receptor binding - 0.7443 74.43%
Androgen receptor binding - 0.8020 80.20%
Thyroid receptor binding - 0.8171 81.71%
Glucocorticoid receptor binding - 0.7966 79.66%
Aromatase binding - 0.6916 69.16%
PPAR gamma - 0.5465 54.65%
Honey bee toxicity - 0.9778 97.78%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9824 98.24%

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
CHEMBL221 P23219 Cyclooxygenase-1 96.47% 90.17%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 95.61% 94.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.81% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.36% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.89% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.83% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.61% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.72% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 80.21% 94.73%

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.
Mentha arvensis
Mentha canadensis

Cross-Links

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PubChem 5367698
NPASS NPC241308