2-Propenoic acid, 3-(2,5-dihydroxyphenyl)-

Details

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Internal ID a1127034-0808-4bd3-935b-82ebaa78cd62
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives > Hydroxycinnamic acids
IUPAC Name 3-(2,5-dihydroxyphenyl)prop-2-enoic acid
SMILES (Canonical) C1=CC(=C(C=C1O)C=CC(=O)O)O
SMILES (Isomeric) C1=CC(=C(C=C1O)C=CC(=O)O)O
InChI InChI=1S/C9H8O4/c10-7-2-3-8(11)6(5-7)1-4-9(12)13/h1-5,10-11H,(H,12,13)
InChI Key JXIPYOZBOMUUCA-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C9H8O4
Molecular Weight 180.16 g/mol
Exact Mass 180.04225873 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.20
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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AKOS028111155
FT-0610383
Q4596785

2D Structure

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2D Structure of 2-Propenoic acid, 3-(2,5-dihydroxyphenyl)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9899 98.99%
Caco-2 + 0.6542 65.42%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8843 88.43%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9057 90.57%
OATP1B3 inhibitior + 0.9696 96.96%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9172 91.72%
P-glycoprotein inhibitior - 0.9901 99.01%
P-glycoprotein substrate - 0.9701 97.01%
CYP3A4 substrate - 0.7088 70.88%
CYP2C9 substrate - 0.6124 61.24%
CYP2D6 substrate - 0.8682 86.82%
CYP3A4 inhibition - 0.8478 84.78%
CYP2C9 inhibition - 0.7138 71.38%
CYP2C19 inhibition - 0.6625 66.25%
CYP2D6 inhibition - 0.9528 95.28%
CYP1A2 inhibition - 0.8776 87.76%
CYP2C8 inhibition - 0.6581 65.81%
CYP inhibitory promiscuity - 0.8138 81.38%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7027 70.27%
Carcinogenicity (trinary) Non-required 0.6768 67.68%
Eye corrosion - 0.5776 57.76%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.8932 89.32%
Skin corrosion - 0.9382 93.82%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8951 89.51%
Micronuclear + 0.7900 79.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation + 0.8667 86.67%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity - 0.6217 62.17%
Acute Oral Toxicity (c) III 0.5745 57.45%
Estrogen receptor binding - 0.6900 69.00%
Androgen receptor binding + 0.5634 56.34%
Thyroid receptor binding - 0.6594 65.94%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding - 0.6666 66.66%
PPAR gamma - 0.5143 51.43%
Honey bee toxicity - 0.9547 95.47%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.8000 80.00%
Fish aquatic toxicity + 0.9834 98.34%

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 96.94% 91.11%
CHEMBL3194 P02766 Transthyretin 95.06% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.58% 95.56%
CHEMBL242 Q92731 Estrogen receptor beta 89.69% 98.35%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.05% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.19% 86.33%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 85.25% 91.71%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 84.19% 98.11%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 83.70% 94.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.78% 99.17%
CHEMBL4208 P20618 Proteasome component C5 80.89% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.32% 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.
Grevillea robusta
Tussilago farfara

Cross-Links

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PubChem 181581
NPASS NPC7901
LOTUS LTS0091994
wikiData Q4596785