2-hydroxy-6-methylpyran-4-one

Details

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Internal ID f2f91a0b-e9d0-4804-ba3a-dc20303c1ea2
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 2-hydroxy-6-methylpyran-4-one
SMILES (Canonical) CC1=CC(=O)C=C(O1)O
SMILES (Isomeric) CC1=CC(=O)C=C(O1)O
InChI InChI=1S/C6H6O3/c1-4-2-5(7)3-6(8)9-4/h2-3,8H,1H3
InChI Key OOKCZXGEYPSNIM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C6H6O3
Molecular Weight 126.11 g/mol
Exact Mass 126.031694049 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP -0.40
Atomic LogP (AlogP) 0.65
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-hydroxy-6-methylpyran-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9879 98.79%
Caco-2 + 0.9230 92.30%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.8328 83.28%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9048 90.48%
OATP1B3 inhibitior + 0.9896 98.96%
MATE1 inhibitior - 0.6600 66.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9373 93.73%
P-glycoprotein inhibitior - 0.9773 97.73%
P-glycoprotein substrate - 0.9901 99.01%
CYP3A4 substrate - 0.6822 68.22%
CYP2C9 substrate - 0.6117 61.17%
CYP2D6 substrate - 0.8645 86.45%
CYP3A4 inhibition - 0.8931 89.31%
CYP2C9 inhibition - 0.9695 96.95%
CYP2C19 inhibition - 0.9279 92.79%
CYP2D6 inhibition - 0.9814 98.14%
CYP1A2 inhibition - 0.7682 76.82%
CYP2C8 inhibition - 0.9763 97.63%
CYP inhibitory promiscuity - 0.9533 95.33%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7958 79.58%
Carcinogenicity (trinary) Non-required 0.6143 61.43%
Eye corrosion + 0.7320 73.20%
Eye irritation + 0.9855 98.55%
Skin irritation + 0.9197 91.97%
Skin corrosion - 0.7250 72.50%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7362 73.62%
Micronuclear + 0.6881 68.81%
Hepatotoxicity + 0.6033 60.33%
skin sensitisation - 0.8514 85.14%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.5943 59.43%
Acute Oral Toxicity (c) III 0.7964 79.64%
Estrogen receptor binding - 0.9061 90.61%
Androgen receptor binding - 0.6958 69.58%
Thyroid receptor binding - 0.8223 82.23%
Glucocorticoid receptor binding - 0.7807 78.07%
Aromatase binding - 0.8544 85.44%
PPAR gamma - 0.7481 74.81%
Honey bee toxicity - 0.9778 97.78%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity - 0.5000 50.00%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.51% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.42% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 91.00% 94.73%
CHEMBL2581 P07339 Cathepsin D 88.68% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.95% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.62% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.30% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.47% 89.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.60% 93.65%

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 12663
LOTUS LTS0007091
wikiData Q105195418