3-Phenyl-propanoic acid propyl ester

Details

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Internal ID 0f1c177e-28e5-4153-b552-aab6ce933385
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name propyl 3-phenylpropanoate
SMILES (Canonical) CCCOC(=O)CCC1=CC=CC=C1
SMILES (Isomeric) CCCOC(=O)CCC1=CC=CC=C1
InChI InChI=1S/C12H16O2/c1-2-10-14-12(13)9-8-11-6-4-3-5-7-11/h3-7H,2,8-10H2,1H3
InChI Key PKIACAVLEKTYRW-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O2
Molecular Weight 192.25 g/mol
Exact Mass 192.115029749 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.57
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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Propyl 3-phenyl propionate
13326-06-2
SCHEMBL3851800
DTXSID201030325
AKOS008947910

2D Structure

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2D Structure of 3-Phenyl-propanoic acid propyl ester

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 + 0.9601 96.01%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Plasma membrane 0.5069 50.69%
OATP2B1 inhibitior - 0.8572 85.72%
OATP1B1 inhibitior + 0.8700 87.00%
OATP1B3 inhibitior + 0.9472 94.72%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6232 62.32%
P-glycoprotein inhibitior - 0.9748 97.48%
P-glycoprotein substrate - 0.8857 88.57%
CYP3A4 substrate - 0.6050 60.50%
CYP2C9 substrate - 0.6120 61.20%
CYP2D6 substrate - 0.8350 83.50%
CYP3A4 inhibition - 0.9429 94.29%
CYP2C9 inhibition - 0.8108 81.08%
CYP2C19 inhibition - 0.6230 62.30%
CYP2D6 inhibition - 0.9017 90.17%
CYP1A2 inhibition + 0.6569 65.69%
CYP2C8 inhibition + 0.5632 56.32%
CYP inhibitory promiscuity - 0.6881 68.81%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.5075 50.75%
Eye corrosion + 0.7067 70.67%
Eye irritation + 0.9474 94.74%
Skin irritation - 0.6181 61.81%
Skin corrosion - 0.9936 99.36%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4359 43.59%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5054 50.54%
skin sensitisation + 0.4898 48.98%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.8121 81.21%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity - 0.6919 69.19%
Acute Oral Toxicity (c) III 0.8062 80.62%
Estrogen receptor binding - 0.8975 89.75%
Androgen receptor binding - 0.7869 78.69%
Thyroid receptor binding - 0.7697 76.97%
Glucocorticoid receptor binding - 0.7876 78.76%
Aromatase binding - 0.7880 78.80%
PPAR gamma - 0.7888 78.88%
Honey bee toxicity - 0.9715 97.15%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9784 97.84%

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 97.67% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.06% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 94.36% 90.17%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 94.16% 94.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.75% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.34% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 83.21% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.04% 95.50%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 81.56% 92.08%

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.
Baccharis dracunculifolia

Cross-Links

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PubChem 21572620
LOTUS LTS0218108
wikiData Q104667233