5-(1-Hydroxy-2-oxobutyl)-4-methoxy-6-methylpyran-2-one

Details

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Internal ID cc0f71b2-83f9-4b00-bab5-d0973d9f1a35
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 5-(1-hydroxy-2-oxobutyl)-4-methoxy-6-methylpyran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H14O5/c1-4-7(12)11(14)10-6(2)16-9(13)5-8(10)15-3/h5,11,14H,4H2,1-3H3
InChI Key XFUASGOQVURFSC-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) 72.80 Ų
XlogP -0.10
Atomic LogP (AlogP) 0.97
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-(1-Hydroxy-2-oxobutyl)-4-methoxy-6-methylpyran-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9155 91.55%
Caco-2 + 0.6440 64.40%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8031 80.31%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior + 0.8860 88.60%
OATP1B3 inhibitior + 0.9191 91.91%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7644 76.44%
P-glycoprotein inhibitior - 0.9101 91.01%
P-glycoprotein substrate - 0.8830 88.30%
CYP3A4 substrate - 0.5768 57.68%
CYP2C9 substrate - 0.5775 57.75%
CYP2D6 substrate - 0.8413 84.13%
CYP3A4 inhibition - 0.9643 96.43%
CYP2C9 inhibition - 0.9368 93.68%
CYP2C19 inhibition - 0.8154 81.54%
CYP2D6 inhibition - 0.9415 94.15%
CYP1A2 inhibition - 0.8632 86.32%
CYP2C8 inhibition - 0.7612 76.12%
CYP inhibitory promiscuity - 0.9279 92.79%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8915 89.15%
Carcinogenicity (trinary) Non-required 0.6949 69.49%
Eye corrosion - 0.9405 94.05%
Eye irritation + 0.6979 69.79%
Skin irritation - 0.7958 79.58%
Skin corrosion - 0.9520 95.20%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4323 43.23%
Micronuclear + 0.5577 55.77%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.8790 87.90%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity - 0.8548 85.48%
Acute Oral Toxicity (c) III 0.5854 58.54%
Estrogen receptor binding - 0.5322 53.22%
Androgen receptor binding - 0.5546 55.46%
Thyroid receptor binding - 0.7221 72.21%
Glucocorticoid receptor binding - 0.7221 72.21%
Aromatase binding - 0.7636 76.36%
PPAR gamma - 0.7893 78.93%
Honey bee toxicity - 0.9461 94.61%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.7028 70.28%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.52% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.17% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 91.99% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 91.29% 97.21%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.92% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.86% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.58% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.23% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.81% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.76% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.71% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.79% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.26% 89.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.13% 90.71%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.49% 86.92%
CHEMBL3401 O75469 Pregnane X receptor 83.21% 94.73%
CHEMBL4208 P20618 Proteasome component C5 82.91% 90.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.25% 95.50%
CHEMBL2535 P11166 Glucose transporter 81.39% 98.75%

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 163066312
LOTUS LTS0028157
wikiData Q104200946