4-(4-Hydroxyphenethoxy)-4-oxobutanoic acid

Details

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Internal ID 22c6ad61-71af-4bc0-af41-1da22210ce2c
Taxonomy Benzenoids > Phenols > Tyrosols and derivatives
IUPAC Name 4-[2-(4-hydroxyphenyl)ethoxy]-4-oxobutanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H14O5/c13-10-3-1-9(2-4-10)7-8-17-12(16)6-5-11(14)15/h1-4,13H,5-8H2,(H,14,15)
InChI Key CVLYVXSOQKJPAE-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H14O5
Molecular Weight 238.24 g/mol
Exact Mass 238.08412354 g/mol
Topological Polar Surface Area (TPSA) 83.80 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.34
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(4-Hydroxyphenethoxy)-4-oxobutanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9801 98.01%
Caco-2 + 0.8191 81.91%
Blood Brain Barrier - 0.8500 85.00%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.9657 96.57%
OATP2B1 inhibitior - 0.8592 85.92%
OATP1B1 inhibitior + 0.8692 86.92%
OATP1B3 inhibitior + 0.9362 93.62%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8542 85.42%
BSEP inhibitior - 0.8540 85.40%
P-glycoprotein inhibitior - 0.9673 96.73%
P-glycoprotein substrate - 0.9137 91.37%
CYP3A4 substrate - 0.5877 58.77%
CYP2C9 substrate + 0.6241 62.41%
CYP2D6 substrate - 0.8308 83.08%
CYP3A4 inhibition - 0.9117 91.17%
CYP2C9 inhibition - 0.9252 92.52%
CYP2C19 inhibition - 0.8006 80.06%
CYP2D6 inhibition - 0.9475 94.75%
CYP1A2 inhibition - 0.9253 92.53%
CYP2C8 inhibition + 0.6757 67.57%
CYP inhibitory promiscuity - 0.9669 96.69%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.7314 73.14%
Eye corrosion - 0.9726 97.26%
Eye irritation + 0.9537 95.37%
Skin irritation - 0.8597 85.97%
Skin corrosion - 0.9864 98.64%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6512 65.12%
Micronuclear - 0.8741 87.41%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.9091 90.91%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.6164 61.64%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.8454 84.54%
Acute Oral Toxicity (c) III 0.6874 68.74%
Estrogen receptor binding + 0.6479 64.79%
Androgen receptor binding + 0.5277 52.77%
Thyroid receptor binding - 0.7520 75.20%
Glucocorticoid receptor binding - 0.4633 46.33%
Aromatase binding - 0.6431 64.31%
PPAR gamma + 0.7362 73.62%
Honey bee toxicity - 0.8746 87.46%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.9226 92.26%

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 97.00% 94.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.19% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.83% 99.17%
CHEMBL2581 P07339 Cathepsin D 90.20% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.97% 94.45%
CHEMBL4040 P28482 MAP kinase ERK2 89.87% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.96% 91.11%
CHEMBL3437 Q16853 Amine oxidase, copper containing 88.03% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.67% 86.33%

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 102531637
LOTUS LTS0108714
wikiData Q77495313