6-butan-2-yl-3-ethyl-2-hydroxypyran-4-one

Details

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Internal ID 26e6c7d4-4908-4b7a-ab73-70c1994d5a7e
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 6-butan-2-yl-3-ethyl-2-hydroxypyran-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H16O3/c1-4-7(3)10-6-9(12)8(5-2)11(13)14-10/h6-7,13H,4-5H2,1-3H3
InChI Key ALTAYLSYXPFNDL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H16O3
Molecular Weight 196.24 g/mol
Exact Mass 196.109944368 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.42
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-butan-2-yl-3-ethyl-2-hydroxypyran-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 + 0.9874 98.74%
Caco-2 + 0.9125 91.25%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.8287 82.87%
OATP2B1 inhibitior - 0.8541 85.41%
OATP1B1 inhibitior + 0.7975 79.75%
OATP1B3 inhibitior + 0.9641 96.41%
MATE1 inhibitior - 0.6800 68.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7390 73.90%
P-glycoprotein inhibitior - 0.9276 92.76%
P-glycoprotein substrate - 0.9605 96.05%
CYP3A4 substrate - 0.7082 70.82%
CYP2C9 substrate + 0.6262 62.62%
CYP2D6 substrate - 0.8343 83.43%
CYP3A4 inhibition - 0.9482 94.82%
CYP2C9 inhibition - 0.8168 81.68%
CYP2C19 inhibition - 0.7894 78.94%
CYP2D6 inhibition - 0.9590 95.90%
CYP1A2 inhibition - 0.7190 71.90%
CYP2C8 inhibition - 0.9773 97.73%
CYP inhibitory promiscuity - 0.8802 88.02%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8228 82.28%
Carcinogenicity (trinary) Non-required 0.6715 67.15%
Eye corrosion - 0.8775 87.75%
Eye irritation - 0.6324 63.24%
Skin irritation - 0.5566 55.66%
Skin corrosion - 0.8676 86.76%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5475 54.75%
Micronuclear - 0.5441 54.41%
Hepatotoxicity + 0.5783 57.83%
skin sensitisation - 0.5590 55.90%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.5510 55.10%
Acute Oral Toxicity (c) III 0.6478 64.78%
Estrogen receptor binding - 0.6661 66.61%
Androgen receptor binding - 0.5164 51.64%
Thyroid receptor binding - 0.5718 57.18%
Glucocorticoid receptor binding - 0.8173 81.73%
Aromatase binding - 0.7745 77.45%
PPAR gamma - 0.6107 61.07%
Honey bee toxicity - 0.9754 97.54%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9309 93.09%

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
CHEMBL2581 P07339 Cathepsin D 96.46% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.70% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.21% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 91.01% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.42% 95.56%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 86.81% 89.34%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.58% 90.71%
CHEMBL1937 Q92769 Histone deacetylase 2 83.61% 94.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.30% 89.00%

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 192528
LOTUS LTS0131825
wikiData Q82910071