p-Coumaroyl glycolic acid

Details

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Internal ID b6a1ebcf-6793-4da7-8ce6-3931280a7b22
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives
IUPAC Name (E)-2-hydroxy-5-(4-hydroxyphenyl)-3-oxopent-4-enoic acid
SMILES (Canonical) C1=CC(=CC=C1C=CC(=O)C(C(=O)O)O)O
SMILES (Isomeric) C1=CC(=CC=C1/C=C/C(=O)C(C(=O)O)O)O
InChI InChI=1S/C11H10O5/c12-8-4-1-7(2-5-8)3-6-9(13)10(14)11(15)16/h1-6,10,12,14H,(H,15,16)/b6-3+
InChI Key ICGTVTIBYULVLN-ZZXKWVIFSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C11H10O5
Molecular Weight 222.19 g/mol
Exact Mass 222.05282342 g/mol
Topological Polar Surface Area (TPSA) 94.80 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.42
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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DTXSID801341831

2D Structure

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2D Structure of p-Coumaroyl glycolic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9465 94.65%
Caco-2 - 0.6558 65.58%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.7913 79.13%
OATP2B1 inhibitior - 0.8601 86.01%
OATP1B1 inhibitior + 0.9221 92.21%
OATP1B3 inhibitior + 0.9732 97.32%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8762 87.62%
P-glycoprotein inhibitior - 0.9788 97.88%
P-glycoprotein substrate - 0.9739 97.39%
CYP3A4 substrate - 0.7077 70.77%
CYP2C9 substrate - 0.5998 59.98%
CYP2D6 substrate - 0.8560 85.60%
CYP3A4 inhibition - 0.7956 79.56%
CYP2C9 inhibition - 0.8997 89.97%
CYP2C19 inhibition - 0.9677 96.77%
CYP2D6 inhibition - 0.9598 95.98%
CYP1A2 inhibition - 0.9392 93.92%
CYP2C8 inhibition - 0.6902 69.02%
CYP inhibitory promiscuity - 0.9757 97.57%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7036 70.36%
Carcinogenicity (trinary) Non-required 0.5835 58.35%
Eye corrosion - 0.9012 90.12%
Eye irritation + 0.9520 95.20%
Skin irritation + 0.7621 76.21%
Skin corrosion - 0.8012 80.12%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9195 91.95%
Micronuclear + 0.7900 79.00%
Hepatotoxicity - 0.6661 66.61%
skin sensitisation + 0.5964 59.64%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity - 0.7038 70.38%
Acute Oral Toxicity (c) III 0.4873 48.73%
Estrogen receptor binding - 0.5781 57.81%
Androgen receptor binding + 0.6119 61.19%
Thyroid receptor binding - 0.7495 74.95%
Glucocorticoid receptor binding + 0.5644 56.44%
Aromatase binding + 0.6679 66.79%
PPAR gamma + 0.5492 54.92%
Honey bee toxicity - 0.9217 92.17%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity + 0.9624 96.24%

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
CHEMBL4040 P28482 MAP kinase ERK2 93.34% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.92% 91.11%
CHEMBL3194 P02766 Transthyretin 89.83% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.67% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.55% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.07% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.41% 86.33%
CHEMBL2581 P07339 Cathepsin D 85.19% 98.95%
CHEMBL242 Q92731 Estrogen receptor beta 84.45% 98.35%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.70% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.52% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.11% 93.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.06% 89.00%

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 129720117
LOTUS LTS0174718
wikiData Q105110975