Albidopyrone

Details

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Internal ID 22c5eb80-da93-4a78-a070-e292d79b94bf
Taxonomy Benzenoids > Benzene and substituted derivatives > Anilides > Acetanilides
IUPAC Name N-[4-(4-hydroxy-5-methyl-6-oxopyran-2-yl)phenyl]acetamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H13NO4/c1-8-12(17)7-13(19-14(8)18)10-3-5-11(6-4-10)15-9(2)16/h3-7,17H,1-2H3,(H,15,16)
InChI Key OJLVTODNXKOZMV-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H13NO4
Molecular Weight 259.26 g/mol
Exact Mass 259.08445790 g/mol
Topological Polar Surface Area (TPSA) 75.60 Ų
XlogP 1.30
Atomic LogP (AlogP) 2.28
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Albidopyrone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8220 82.20%
Caco-2 + 0.7073 70.73%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7805 78.05%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9522 95.22%
OATP1B3 inhibitior + 0.9342 93.42%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.4771 47.71%
P-glycoprotein inhibitior - 0.9403 94.03%
P-glycoprotein substrate - 0.9149 91.49%
CYP3A4 substrate + 0.5090 50.90%
CYP2C9 substrate + 0.6202 62.02%
CYP2D6 substrate - 0.8909 89.09%
CYP3A4 inhibition - 0.9333 93.33%
CYP2C9 inhibition - 0.8286 82.86%
CYP2C19 inhibition - 0.7917 79.17%
CYP2D6 inhibition - 0.9460 94.60%
CYP1A2 inhibition - 0.9840 98.40%
CYP2C8 inhibition - 0.7807 78.07%
CYP inhibitory promiscuity - 0.8153 81.53%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8011 80.11%
Carcinogenicity (trinary) Non-required 0.6060 60.60%
Eye corrosion - 0.9956 99.56%
Eye irritation - 0.7522 75.22%
Skin irritation - 0.8399 83.99%
Skin corrosion - 0.9702 97.02%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5775 57.75%
Micronuclear + 0.9100 91.00%
Hepatotoxicity + 0.6950 69.50%
skin sensitisation - 0.9377 93.77%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.6153 61.53%
Acute Oral Toxicity (c) III 0.6874 68.74%
Estrogen receptor binding + 0.9104 91.04%
Androgen receptor binding + 0.8249 82.49%
Thyroid receptor binding + 0.5531 55.31%
Glucocorticoid receptor binding + 0.8561 85.61%
Aromatase binding + 0.8333 83.33%
PPAR gamma + 0.7046 70.46%
Honey bee toxicity - 0.9537 95.37%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9484 94.84%

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
CHEMBL1293277 O15118 Niemann-Pick C1 protein 97.16% 81.11%
CHEMBL3401 O75469 Pregnane X receptor 95.51% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.48% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.45% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.26% 94.00%
CHEMBL1913 P09619 Platelet-derived growth factor receptor beta 91.98% 95.70%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 89.69% 97.21%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 89.43% 87.67%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.95% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.09% 99.23%
CHEMBL4530 P00488 Coagulation factor XIII 87.78% 96.00%
CHEMBL1951 P21397 Monoamine oxidase A 87.65% 91.49%
CHEMBL3085 P43003 Excitatory amino acid transporter 1 86.81% 94.67%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.73% 90.71%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.75% 99.15%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.98% 94.45%
CHEMBL3038469 P24941 CDK2/Cyclin A 84.02% 91.38%
CHEMBL340 P08684 Cytochrome P450 3A4 83.87% 91.19%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.20% 94.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.39% 85.14%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.38% 95.50%
CHEMBL2581 P07339 Cathepsin D 81.07% 98.95%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.94% 94.42%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.60% 86.33%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 80.50% 92.29%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.35% 97.28%

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 54740233
LOTUS LTS0010895
wikiData Q77571343