Isopropyl 3-phenylpropionate

Details

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Internal ID 42082596-9bcc-4dbb-b7d7-2f003d90a956
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name propan-2-yl 3-phenylpropanoate
SMILES (Canonical) CC(C)OC(=O)CCC1=CC=CC=C1
SMILES (Isomeric) CC(C)OC(=O)CCC1=CC=CC=C1
InChI InChI=1S/C12H16O2/c1-10(2)14-12(13)9-8-11-6-4-3-5-7-11/h3-7,10H,8-9H2,1-2H3
InChI Key YQPAOLMOGAHRLG-UHFFFAOYSA-N
Popularity 7 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 3.10
Atomic LogP (AlogP) 2.57
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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22767-95-9
3-phenyl-propanoic acid 1-methylethyl ester
NSC406208
Isopropyl 3-phenylpropanoate #
SCHEMBL3183513
DTXSID80324271
AKOS008947909
NSC-406208
3-Phenylpropionic acid, isopropyl ester
3-Phenyl-propionic acid, isopropyl ester
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isopropyl 3-phenylpropionate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9965 99.65%
Caco-2 + 0.9561 95.61%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7829 78.29%
OATP2B1 inhibitior - 0.8657 86.57%
OATP1B1 inhibitior + 0.9216 92.16%
OATP1B3 inhibitior + 0.9481 94.81%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8007 80.07%
P-glycoprotein inhibitior - 0.9757 97.57%
P-glycoprotein substrate - 0.8389 83.89%
CYP3A4 substrate - 0.6396 63.96%
CYP2C9 substrate - 0.6120 61.20%
CYP2D6 substrate - 0.8350 83.50%
CYP3A4 inhibition - 0.9629 96.29%
CYP2C9 inhibition - 0.8803 88.03%
CYP2C19 inhibition - 0.8732 87.32%
CYP2D6 inhibition - 0.9376 93.76%
CYP1A2 inhibition - 0.6419 64.19%
CYP2C8 inhibition - 0.8147 81.47%
CYP inhibitory promiscuity - 0.7282 72.82%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5311 53.11%
Carcinogenicity (trinary) Non-required 0.6028 60.28%
Eye corrosion + 0.7152 71.52%
Eye irritation + 0.9218 92.18%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9823 98.23%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5600 56.00%
Micronuclear - 0.9515 95.15%
Hepatotoxicity + 0.5587 55.87%
skin sensitisation + 0.6591 65.91%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity - 0.6566 65.66%
Acute Oral Toxicity (c) III 0.5452 54.52%
Estrogen receptor binding - 0.9051 90.51%
Androgen receptor binding - 0.7542 75.42%
Thyroid receptor binding - 0.7833 78.33%
Glucocorticoid receptor binding - 0.6582 65.82%
Aromatase binding - 0.7671 76.71%
PPAR gamma - 0.8387 83.87%
Honey bee toxicity - 0.8966 89.66%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5045 50.45%
Fish aquatic toxicity + 0.6871 68.71%

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
CHEMBL2581 P07339 Cathepsin D 96.37% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.92% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 87.88% 94.62%
CHEMBL3401 O75469 Pregnane X receptor 87.53% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.39% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 87.26% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.10% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.65% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.48% 99.17%

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 347496
LOTUS LTS0118785
wikiData Q82083809