6-(6-Hydroxy-3-methyl-4-oxohexan-3-yl)-2,3-dimethylpyran-4-one

Details

Top
Internal ID 269fe8a6-8863-4921-a69d-200cbeaf2f54
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 6-(6-hydroxy-3-methyl-4-oxohexan-3-yl)-2,3-dimethylpyran-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H20O4/c1-5-14(4,12(17)6-7-15)13-8-11(16)9(2)10(3)18-13/h8,15H,5-7H2,1-4H3
InChI Key MBIIMOIHBGURSP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C14H20O4
Molecular Weight 252.31 g/mol
Exact Mass 252.13615911 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.88
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 6-(6-Hydroxy-3-methyl-4-oxohexan-3-yl)-2,3-dimethylpyran-4-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9863 98.63%
Caco-2 + 0.9511 95.11%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.8364 83.64%
OATP2B1 inhibitior - 0.8517 85.17%
OATP1B1 inhibitior + 0.8821 88.21%
OATP1B3 inhibitior + 0.9229 92.29%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.6440 64.40%
P-glycoprotein inhibitior - 0.9336 93.36%
P-glycoprotein substrate - 0.8324 83.24%
CYP3A4 substrate - 0.5781 57.81%
CYP2C9 substrate - 0.5979 59.79%
CYP2D6 substrate - 0.8462 84.62%
CYP3A4 inhibition + 0.7387 73.87%
CYP2C9 inhibition - 0.8561 85.61%
CYP2C19 inhibition - 0.8141 81.41%
CYP2D6 inhibition - 0.9328 93.28%
CYP1A2 inhibition - 0.6671 66.71%
CYP2C8 inhibition - 0.8640 86.40%
CYP inhibitory promiscuity - 0.9553 95.53%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.7236 72.36%
Eye corrosion - 0.9856 98.56%
Eye irritation - 0.5483 54.83%
Skin irritation - 0.7475 74.75%
Skin corrosion - 0.9683 96.83%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6449 64.49%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.5033 50.33%
skin sensitisation - 0.8259 82.59%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.7026 70.26%
Acute Oral Toxicity (c) III 0.6500 65.00%
Estrogen receptor binding - 0.6967 69.67%
Androgen receptor binding + 0.5355 53.55%
Thyroid receptor binding - 0.6800 68.00%
Glucocorticoid receptor binding - 0.5767 57.67%
Aromatase binding - 0.5743 57.43%
PPAR gamma + 0.5231 52.31%
Honey bee toxicity - 0.9576 95.76%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity + 0.9259 92.59%

Targets

Top

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 94.68% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.62% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.59% 97.25%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.47% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 88.99% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.33% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.17% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.60% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.62% 96.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.33% 94.00%

Plants that contains it

Top
Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

Top
PubChem 23250366
LOTUS LTS0243175
wikiData Q105160771