1-Piperidin-2-ylpentan-2-one

Details

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Internal ID b8d0e844-3d9d-4b0e-b983-869782e4105c
Taxonomy Organoheterocyclic compounds > Piperidines
IUPAC Name 1-piperidin-2-ylpentan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H19NO/c1-2-5-10(12)8-9-6-3-4-7-11-9/h9,11H,2-8H2,1H3
InChI Key RKAFWGMBQWSOAC-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C10H19NO
Molecular Weight 169.26 g/mol
Exact Mass 169.146664230 g/mol
Topological Polar Surface Area (TPSA) 29.10 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.89
H-Bond Acceptor 2
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 1-Piperidin-2-ylpentan-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 + 0.9949 99.49%
Caco-2 + 0.8500 85.00%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.5292 52.92%
OATP2B1 inhibitior - 0.8448 84.48%
OATP1B1 inhibitior + 0.9358 93.58%
OATP1B3 inhibitior + 0.9438 94.38%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior - 0.8953 89.53%
P-glycoprotein inhibitior - 0.9700 97.00%
P-glycoprotein substrate - 0.8033 80.33%
CYP3A4 substrate - 0.6116 61.16%
CYP2C9 substrate - 0.8108 81.08%
CYP2D6 substrate + 0.4237 42.37%
CYP3A4 inhibition - 0.9624 96.24%
CYP2C9 inhibition - 0.8887 88.87%
CYP2C19 inhibition - 0.9330 93.30%
CYP2D6 inhibition - 0.7044 70.44%
CYP1A2 inhibition - 0.5284 52.84%
CYP2C8 inhibition - 0.8945 89.45%
CYP inhibitory promiscuity - 0.9292 92.92%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.7255 72.55%
Eye corrosion - 0.6042 60.42%
Eye irritation + 0.9317 93.17%
Skin irritation - 0.5583 55.83%
Skin corrosion - 0.5392 53.92%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6673 66.73%
Micronuclear - 0.8300 83.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.8190 81.90%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.6326 63.26%
Acute Oral Toxicity (c) III 0.8225 82.25%
Estrogen receptor binding - 0.9279 92.79%
Androgen receptor binding - 0.8237 82.37%
Thyroid receptor binding - 0.8351 83.51%
Glucocorticoid receptor binding - 0.8822 88.22%
Aromatase binding - 0.8624 86.24%
PPAR gamma - 0.8575 85.75%
Honey bee toxicity - 0.9883 98.83%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.6632 66.32%
Fish aquatic toxicity - 0.9191 91.91%

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 93.74% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.32% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.24% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.22% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.88% 94.45%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 86.22% 93.03%
CHEMBL5255 O00206 Toll-like receptor 4 85.44% 92.50%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.50% 95.50%
CHEMBL218 P21554 Cannabinoid CB1 receptor 82.47% 96.61%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.40% 92.62%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 82.00% 97.50%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.56% 94.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.04% 99.23%

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.
Sedum lancerottense

Cross-Links

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PubChem 73083019
LOTUS LTS0098274
wikiData Q105238265