4-Hydroxy-3-(16-methylheptadecyl)-2H-pyran-2-one

Details

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Internal ID 13133b2b-6158-4a3d-be6e-5a39085bbced
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 4-hydroxy-3-(16-methylheptadecyl)pyran-2-one
SMILES (Canonical) CC(C)CCCCCCCCCCCCCCCC1=C(C=COC1=O)O
SMILES (Isomeric) CC(C)CCCCCCCCCCCCCCCC1=C(C=COC1=O)O
InChI InChI=1S/C23H40O3/c1-20(2)16-14-12-10-8-6-4-3-5-7-9-11-13-15-17-21-22(24)18-19-26-23(21)25/h18-20,24H,3-17H2,1-2H3
InChI Key XEKYYIHOWASTHE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H40O3
Molecular Weight 364.60 g/mol
Exact Mass 364.29774513 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 9.30
Atomic LogP (AlogP) 7.01
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 16

Synonyms

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DTXSID201236890
3-(16-Methylheptadecyl)-4-hydroxy-2-pyrone
203300-23-6

2D Structure

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2D Structure of 4-Hydroxy-3-(16-methylheptadecyl)-2H-pyran-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 + 0.9810 98.10%
Caco-2 + 0.5263 52.63%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8846 88.46%
OATP2B1 inhibitior - 0.8518 85.18%
OATP1B1 inhibitior + 0.9264 92.64%
OATP1B3 inhibitior + 0.9444 94.44%
MATE1 inhibitior - 0.6800 68.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.5965 59.65%
P-glycoprotein inhibitior - 0.5871 58.71%
P-glycoprotein substrate - 0.8489 84.89%
CYP3A4 substrate - 0.5332 53.32%
CYP2C9 substrate + 0.7396 73.96%
CYP2D6 substrate - 0.8707 87.07%
CYP3A4 inhibition - 0.6806 68.06%
CYP2C9 inhibition - 0.5788 57.88%
CYP2C19 inhibition - 0.5685 56.85%
CYP2D6 inhibition - 0.8822 88.22%
CYP1A2 inhibition - 0.6136 61.36%
CYP2C8 inhibition - 0.9206 92.06%
CYP inhibitory promiscuity - 0.8811 88.11%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8615 86.15%
Carcinogenicity (trinary) Non-required 0.7318 73.18%
Eye corrosion - 0.9434 94.34%
Eye irritation + 0.6932 69.32%
Skin irritation - 0.6614 66.14%
Skin corrosion - 0.8405 84.05%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5715 57.15%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.5618 56.18%
skin sensitisation - 0.6464 64.64%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.5497 54.97%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.7458 74.58%
Acute Oral Toxicity (c) III 0.5991 59.91%
Estrogen receptor binding - 0.5804 58.04%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding + 0.5529 55.29%
Glucocorticoid receptor binding - 0.5736 57.36%
Aromatase binding - 0.7667 76.67%
PPAR gamma + 0.7984 79.84%
Honey bee toxicity - 0.9696 96.96%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.5238 52.38%
Fish aquatic toxicity + 0.9916 99.16%

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 97.42% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.62% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 93.42% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 93.08% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.34% 95.56%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.55% 93.56%
CHEMBL1937 Q92769 Histone deacetylase 2 84.85% 94.75%
CHEMBL1907 P15144 Aminopeptidase N 84.14% 93.31%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.94% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.93% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.94% 86.33%
CHEMBL2996 Q05655 Protein kinase C delta 80.67% 97.79%

Cross-Links

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PubChem 86187765
NPASS NPC227806