3-Phenylpropyl acetate

Details

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Internal ID 76000a05-0f37-4425-b48d-a50f1a6ae7c7
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 3-phenylpropyl acetate
SMILES (Canonical) CC(=O)OCCCC1=CC=CC=C1
SMILES (Isomeric) CC(=O)OCCCC1=CC=CC=C1
InChI InChI=1S/C11H14O2/c1-10(12)13-9-5-8-11-6-3-2-4-7-11/h2-4,6-7H,5,8-9H2,1H3
InChI Key JRJGKUTZNBZHNK-UHFFFAOYSA-N
Popularity 43 references in papers

Physical and Chemical Properties

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Molecular Formula C11H14O2
Molecular Weight 178.23 g/mol
Exact Mass 178.099379685 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.18
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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122-72-5
Hydrocinnamyl acetate
Benzenepropanol, 1-acetate
Benzenepropanol, acetate
3-Phenyl-1-propyl acetate
Phenylpropyl acetate
(3-Acetoxypropyl)benzene
3-Acetoxy-1-phenylpropane
3-Phenyl-1-propanol, acetate
1-Acetoxy-3-phenylpropane
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Phenylpropyl 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 + 0.9656 96.56%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7384 73.84%
OATP2B1 inhibitior - 0.8633 86.33%
OATP1B1 inhibitior + 0.9050 90.50%
OATP1B3 inhibitior + 0.9434 94.34%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6278 62.78%
P-glycoprotein inhibitior - 0.9822 98.22%
P-glycoprotein substrate - 0.9291 92.91%
CYP3A4 substrate - 0.5718 57.18%
CYP2C9 substrate - 0.6120 61.20%
CYP2D6 substrate - 0.8350 83.50%
CYP3A4 inhibition - 0.9641 96.41%
CYP2C9 inhibition - 0.9320 93.20%
CYP2C19 inhibition - 0.8349 83.49%
CYP2D6 inhibition - 0.9303 93.03%
CYP1A2 inhibition + 0.6451 64.51%
CYP2C8 inhibition - 0.7239 72.39%
CYP inhibitory promiscuity - 0.8098 80.98%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7300 73.00%
Carcinogenicity (trinary) Non-required 0.6391 63.91%
Eye corrosion + 0.7799 77.99%
Eye irritation + 0.9739 97.39%
Skin irritation + 0.8428 84.28%
Skin corrosion - 0.9636 96.36%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6093 60.93%
Micronuclear - 0.9915 99.15%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.5465 54.65%
Respiratory toxicity - 0.9778 97.78%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.5556 55.56%
Acute Oral Toxicity (c) III 0.8560 85.60%
Estrogen receptor binding - 0.7852 78.52%
Androgen receptor binding - 0.5975 59.75%
Thyroid receptor binding - 0.8027 80.27%
Glucocorticoid receptor binding - 0.8025 80.25%
Aromatase binding - 0.7463 74.63%
PPAR gamma - 0.8921 89.21%
Honey bee toxicity - 0.9688 96.88%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.8319 83.19%

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
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 98.00% 94.62%
CHEMBL2581 P07339 Cathepsin D 97.15% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.88% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.47% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.45% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 86.14% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.87% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.67% 91.11%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.18% 95.50%
CHEMBL5028 O14672 ADAM10 80.68% 97.50%

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.
Cucumis melo
Hansenia forbesii
Hansenia weberbaueriana

Cross-Links

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PubChem 31226
NPASS NPC100842
LOTUS LTS0001456
wikiData Q27155198