Tyrosol propionate

Details

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Internal ID 439d2a3f-8a9b-45c6-ae03-46fafa8cce54
Taxonomy Benzenoids > Phenols > Tyrosols and derivatives
IUPAC Name 2-(4-hydroxyphenyl)ethyl propanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H14O3/c1-2-11(13)14-8-7-9-3-5-10(12)6-4-9/h3-6,12H,2,7-8H2,1H3
InChI Key PGQKVDCXCRDUMK-UHFFFAOYSA-N
Popularity 3 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 2.20
Atomic LogP (AlogP) 1.89
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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2-(4-hydroxyphenyl)ethyl propanoate
SCHEMBL8985470
CHEBI:211095

2D Structure

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2D Structure of Tyrosol propionate

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 + 0.9566 95.66%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.8923 89.23%
OATP2B1 inhibitior - 0.8575 85.75%
OATP1B1 inhibitior + 0.8787 87.87%
OATP1B3 inhibitior + 0.9441 94.41%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7942 79.42%
P-glycoprotein inhibitior - 0.9875 98.75%
P-glycoprotein substrate - 0.8564 85.64%
CYP3A4 substrate - 0.5552 55.52%
CYP2C9 substrate - 0.6092 60.92%
CYP2D6 substrate - 0.8168 81.68%
CYP3A4 inhibition - 0.8994 89.94%
CYP2C9 inhibition - 0.8637 86.37%
CYP2C19 inhibition - 0.6274 62.74%
CYP2D6 inhibition - 0.8962 89.62%
CYP1A2 inhibition - 0.5676 56.76%
CYP2C8 inhibition + 0.7795 77.95%
CYP inhibitory promiscuity - 0.8028 80.28%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8123 81.23%
Carcinogenicity (trinary) Non-required 0.6414 64.14%
Eye corrosion - 0.9284 92.84%
Eye irritation + 0.9762 97.62%
Skin irritation - 0.8917 89.17%
Skin corrosion - 0.9891 98.91%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6549 65.49%
Micronuclear - 0.9582 95.82%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation - 0.8042 80.42%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.8885 88.85%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity - 0.7813 78.13%
Acute Oral Toxicity (c) III 0.8148 81.48%
Estrogen receptor binding - 0.6495 64.95%
Androgen receptor binding + 0.5480 54.80%
Thyroid receptor binding - 0.7627 76.27%
Glucocorticoid receptor binding - 0.6983 69.83%
Aromatase binding - 0.6384 63.84%
PPAR gamma + 0.5747 57.47%
Honey bee toxicity - 0.9154 91.54%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.5850 58.50%
Fish aquatic toxicity + 0.9360 93.60%

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 97.12% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.22% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.57% 94.45%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 89.06% 94.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.79% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.94% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.30% 96.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.12% 91.11%
CHEMBL3437 Q16853 Amine oxidase, copper containing 82.43% 94.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.35% 97.25%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.18% 93.65%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 18987910
LOTUS LTS0224932
wikiData Q77492874