2-Hydroxyethyl 3-phenylpropionate

Details

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Internal ID 900f5e2c-f976-4092-9c18-052c34a6150e
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name 2-hydroxyethyl 3-phenylpropanoate
SMILES (Canonical) C1=CC=C(C=C1)CCC(=O)OCCO
SMILES (Isomeric) C1=CC=C(C=C1)CCC(=O)OCCO
InChI InChI=1S/C11H14O3/c12-8-9-14-11(13)7-6-10-4-2-1-3-5-10/h1-5,12H,6-9H2
InChI Key YVNBSYGHQJLAIN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H14O3
Molecular Weight 194.23 g/mol
Exact Mass 194.094294304 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.15
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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72143-21-6
EINECS 276-381-4
2-hydroxyethyl 3-phenylpropanoate
SCHEMBL6425149
DTXSID70992867

2D Structure

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2D Structure of 2-Hydroxyethyl 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 + 0.9822 98.22%
Caco-2 + 0.8281 82.81%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.8079 80.79%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8873 88.73%
OATP1B3 inhibitior + 0.9416 94.16%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7493 74.93%
P-glycoprotein inhibitior - 0.9915 99.15%
P-glycoprotein substrate - 0.9365 93.65%
CYP3A4 substrate - 0.6145 61.45%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.8043 80.43%
CYP3A4 inhibition - 0.9454 94.54%
CYP2C9 inhibition - 0.8770 87.70%
CYP2C19 inhibition - 0.8375 83.75%
CYP2D6 inhibition - 0.9582 95.82%
CYP1A2 inhibition - 0.9050 90.50%
CYP2C8 inhibition + 0.4556 45.56%
CYP inhibitory promiscuity - 0.9359 93.59%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.6843 68.43%
Eye corrosion + 0.5257 52.57%
Eye irritation + 0.9668 96.68%
Skin irritation - 0.6277 62.77%
Skin corrosion - 0.9561 95.61%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6404 64.04%
Micronuclear - 0.9541 95.41%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.6078 60.78%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.7568 75.68%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity - 0.6897 68.97%
Acute Oral Toxicity (c) III 0.7045 70.45%
Estrogen receptor binding - 0.8706 87.06%
Androgen receptor binding - 0.7674 76.74%
Thyroid receptor binding - 0.8532 85.32%
Glucocorticoid receptor binding - 0.6569 65.69%
Aromatase binding - 0.6806 68.06%
PPAR gamma - 0.5693 56.93%
Honey bee toxicity - 0.9276 92.76%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.6592 65.92%

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 96.95% 94.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.80% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.71% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.10% 86.33%
CHEMBL2581 P07339 Cathepsin D 89.34% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.22% 91.11%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.44% 95.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.71% 95.56%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 80.33% 92.67%

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.
Oxalis pes-caprae

Cross-Links

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PubChem 3018319
LOTUS LTS0253355
wikiData Q82983332