3-((e)-2-Carboxyethenyl)-5-(4-hydroxyphenyl)-4-pyrone-2-carboxylic acid

Details

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Internal ID f1936f7d-b08e-4ceb-8d42-75fd1f20f91b
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 3-[(E)-2-carboxyethenyl]-5-(4-hydroxyphenyl)-4-oxopyran-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H10O7/c16-9-3-1-8(2-4-9)11-7-22-14(15(20)21)10(13(11)19)5-6-12(17)18/h1-7,16H,(H,17,18)(H,20,21)/b6-5+
InChI Key IMBFSFAPSYRTQN-AATRIKPKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H10O7
Molecular Weight 302.23 g/mol
Exact Mass 302.04265265 g/mol
Topological Polar Surface Area (TPSA) 121.00 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.81
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-((e)-2-Carboxyethenyl)-5-(4-hydroxyphenyl)-4-pyrone-2-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9274 92.74%
Caco-2 - 0.6107 61.07%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7817 78.17%
OATP2B1 inhibitior - 0.5652 56.52%
OATP1B1 inhibitior + 0.9136 91.36%
OATP1B3 inhibitior + 0.9151 91.51%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7897 78.97%
P-glycoprotein inhibitior - 0.9452 94.52%
P-glycoprotein substrate - 0.9262 92.62%
CYP3A4 substrate - 0.5596 55.96%
CYP2C9 substrate - 0.8024 80.24%
CYP2D6 substrate - 0.8936 89.36%
CYP3A4 inhibition - 0.8810 88.10%
CYP2C9 inhibition + 0.8232 82.32%
CYP2C19 inhibition - 0.7159 71.59%
CYP2D6 inhibition - 0.9589 95.89%
CYP1A2 inhibition - 0.9572 95.72%
CYP2C8 inhibition + 0.5786 57.86%
CYP inhibitory promiscuity - 0.6088 60.88%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9128 91.28%
Carcinogenicity (trinary) Non-required 0.6366 63.66%
Eye corrosion - 0.9890 98.90%
Eye irritation + 0.8059 80.59%
Skin irritation - 0.5385 53.85%
Skin corrosion - 0.9399 93.99%
Ames mutagenesis - 0.6723 67.23%
Human Ether-a-go-go-Related Gene inhibition - 0.9344 93.44%
Micronuclear + 0.9000 90.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.7879 78.79%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.7309 73.09%
Acute Oral Toxicity (c) II 0.4745 47.45%
Estrogen receptor binding + 0.6622 66.22%
Androgen receptor binding + 0.8100 81.00%
Thyroid receptor binding - 0.5147 51.47%
Glucocorticoid receptor binding + 0.7494 74.94%
Aromatase binding + 0.7459 74.59%
PPAR gamma + 0.7795 77.95%
Honey bee toxicity - 0.8927 89.27%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9852 98.52%

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
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 93.52% 91.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.52% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.15% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.50% 91.11%
CHEMBL242 Q92731 Estrogen receptor beta 89.32% 98.35%
CHEMBL3194 P02766 Transthyretin 89.32% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.06% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.72% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.47% 99.23%

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 102417063
LOTUS LTS0075913
wikiData Q105115581