Madisone

Details

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Internal ID 4491e2b4-3e40-4e90-959a-2b647bc84753
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 1-[2,4-dihydroxy-3-(2-hydroxyethyl)-6-methoxyphenyl]ethanone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H14O5/c1-6(13)10-9(16-2)5-8(14)7(3-4-12)11(10)15/h5,12,14-15H,3-4H2,1-2H3
InChI Key ANCNXFYJWODNDX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H14O5
Molecular Weight 226.23 g/mol
Exact Mass 226.08412354 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 1.00
Atomic LogP (AlogP) 0.84
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 Madisone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9497 94.97%
Caco-2 + 0.5883 58.83%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8792 87.92%
OATP2B1 inhibitior - 0.8512 85.12%
OATP1B1 inhibitior + 0.8214 82.14%
OATP1B3 inhibitior + 0.9600 96.00%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8905 89.05%
P-glycoprotein inhibitior - 0.9060 90.60%
P-glycoprotein substrate - 0.8050 80.50%
CYP3A4 substrate - 0.5533 55.33%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7961 79.61%
CYP3A4 inhibition - 0.7075 70.75%
CYP2C9 inhibition - 0.7668 76.68%
CYP2C19 inhibition - 0.6932 69.32%
CYP2D6 inhibition - 0.8894 88.94%
CYP1A2 inhibition + 0.6804 68.04%
CYP2C8 inhibition - 0.6136 61.36%
CYP inhibitory promiscuity - 0.7897 78.97%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.7967 79.67%
Eye corrosion - 0.9720 97.20%
Eye irritation + 0.6977 69.77%
Skin irritation - 0.7019 70.19%
Skin corrosion - 0.9414 94.14%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5694 56.94%
Micronuclear - 0.8323 83.23%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.6999 69.99%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.6060 60.60%
Acute Oral Toxicity (c) III 0.7910 79.10%
Estrogen receptor binding + 0.5771 57.71%
Androgen receptor binding - 0.7161 71.61%
Thyroid receptor binding - 0.7026 70.26%
Glucocorticoid receptor binding - 0.5435 54.35%
Aromatase binding - 0.7346 73.46%
PPAR gamma - 0.6156 61.56%
Honey bee toxicity - 0.9330 93.30%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.9004 90.04%
Fish aquatic toxicity - 0.6251 62.51%

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 96.27% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.60% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.18% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.34% 99.17%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 88.29% 86.92%
CHEMBL2581 P07339 Cathepsin D 87.74% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.44% 94.00%
CHEMBL1255126 O15151 Protein Mdm4 83.75% 90.20%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.57% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.09% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.90% 85.14%

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 132529229
LOTUS LTS0090558
wikiData Q103816256