5-Pentyl-2H-pyran-2-one

Details

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Internal ID 912c7324-fb99-4d4e-bf65-5243a200dd0b
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 5-pentylpyran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14O2/c1-2-3-4-5-9-6-7-10(11)12-8-9/h6-8H,2-5H2,1H3
InChI Key YSGNURNGKGAYOX-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O2
Molecular Weight 166.22 g/mol
Exact Mass 166.099379685 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.37
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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23079-71-2
DTXSID90780940

2D Structure

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2D Structure of 5-Pentyl-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 + 0.9955 99.55%
Caco-2 + 0.9605 96.05%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.4746 47.46%
OATP2B1 inhibitior - 0.8598 85.98%
OATP1B1 inhibitior + 0.8654 86.54%
OATP1B3 inhibitior + 0.9460 94.60%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9269 92.69%
P-glycoprotein inhibitior - 0.9837 98.37%
P-glycoprotein substrate - 0.8935 89.35%
CYP3A4 substrate - 0.6404 64.04%
CYP2C9 substrate - 0.6330 63.30%
CYP2D6 substrate - 0.8437 84.37%
CYP3A4 inhibition - 0.8943 89.43%
CYP2C9 inhibition - 0.7298 72.98%
CYP2C19 inhibition - 0.5906 59.06%
CYP2D6 inhibition - 0.8925 89.25%
CYP1A2 inhibition + 0.6567 65.67%
CYP2C8 inhibition - 0.8295 82.95%
CYP inhibitory promiscuity - 0.8453 84.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.5594 55.94%
Eye corrosion + 0.5663 56.63%
Eye irritation + 0.9033 90.33%
Skin irritation + 0.7491 74.91%
Skin corrosion - 0.7295 72.95%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5224 52.24%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation + 0.5091 50.91%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.6304 63.04%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.5581 55.81%
Acute Oral Toxicity (c) III 0.9031 90.31%
Estrogen receptor binding - 0.7666 76.66%
Androgen receptor binding - 0.6164 61.64%
Thyroid receptor binding - 0.7923 79.23%
Glucocorticoid receptor binding - 0.5602 56.02%
Aromatase binding - 0.5437 54.37%
PPAR gamma - 0.6357 63.57%
Honey bee toxicity - 0.9709 97.09%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6450 64.50%
Fish aquatic toxicity + 0.9596 95.96%

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 98.20% 98.95%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 91.96% 85.94%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.58% 92.08%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.86% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 88.88% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.05% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.34% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.04% 94.45%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 84.03% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.78% 99.17%
CHEMBL5805 Q9NR97 Toll-like receptor 8 82.70% 96.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.94% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 80.22% 93.31%

Plants that contains it

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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.
Glycyrrhiza glabra

Cross-Links

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PubChem 71356827
LOTUS LTS0251866
wikiData Q82744459