p-Hydroxycoumaric acid

Details

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Internal ID e1074328-1f12-49c0-9750-138ec0fc0073
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acids
IUPAC Name (E)-3-(4,4-dihydroxycyclohexa-1,5-dien-1-yl)prop-2-enoic acid
SMILES (Canonical) C1C=C(C=CC1(O)O)C=CC(=O)O
SMILES (Isomeric) C1C=C(C=CC1(O)O)/C=C/C(=O)O
InChI InChI=1S/C9H10O4/c10-8(11)2-1-7-3-5-9(12,13)6-4-7/h1-5,12-13H,6H2,(H,10,11)/b2-1+
InChI Key KHQDAOSIOHTJCX-OWOJBTEDSA-N
Popularity 25 references in papers

Physical and Chemical Properties

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Molecular Formula C9H10O4
Molecular Weight 182.17 g/mol
Exact Mass 182.05790880 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP -0.20
Atomic LogP (AlogP) 0.19
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of p-Hydroxycoumaric acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9621 96.21%
Caco-2 + 0.7576 75.76%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8183 81.83%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9503 95.03%
OATP1B3 inhibitior + 0.9405 94.05%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8721 87.21%
P-glycoprotein inhibitior - 0.9856 98.56%
P-glycoprotein substrate - 0.9475 94.75%
CYP3A4 substrate - 0.6122 61.22%
CYP2C9 substrate - 0.5979 59.79%
CYP2D6 substrate - 0.8759 87.59%
CYP3A4 inhibition - 0.9366 93.66%
CYP2C9 inhibition - 0.9485 94.85%
CYP2C19 inhibition - 0.9125 91.25%
CYP2D6 inhibition - 0.9467 94.67%
CYP1A2 inhibition - 0.9560 95.60%
CYP2C8 inhibition - 0.9222 92.22%
CYP inhibitory promiscuity - 0.9684 96.84%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7437 74.37%
Carcinogenicity (trinary) Non-required 0.6534 65.34%
Eye corrosion - 0.8691 86.91%
Eye irritation + 0.9794 97.94%
Skin irritation + 0.6216 62.16%
Skin corrosion - 0.8717 87.17%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8925 89.25%
Micronuclear + 0.5359 53.59%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation + 0.6836 68.36%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.5857 58.57%
Acute Oral Toxicity (c) III 0.6296 62.96%
Estrogen receptor binding - 0.7649 76.49%
Androgen receptor binding - 0.7168 71.68%
Thyroid receptor binding - 0.7269 72.69%
Glucocorticoid receptor binding - 0.6155 61.55%
Aromatase binding - 0.7980 79.80%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.9301 93.01%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.8000 80.00%
Fish aquatic toxicity + 0.6679 66.79%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.56% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 87.29% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.08% 96.09%
CHEMBL4208 P20618 Proteasome component C5 82.91% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.43% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.49% 89.00%

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.
Chromolaena odorata
Phebalium clavatum

Cross-Links

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PubChem 129671844
LOTUS LTS0014687
wikiData Q105141284