1-(1-Methyl-2-piperidyl)-2-butanone

Details

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Internal ID 79449349-7361-4aae-b2a6-d38fc414b0b1
Taxonomy Organoheterocyclic compounds > Piperidines
IUPAC Name 1-(1-methylpiperidin-2-yl)butan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H19NO/c1-3-10(12)8-9-6-4-5-7-11(9)2/h9H,3-8H2,1-2H3
InChI Key CKXIKZSNXVVTDZ-UHFFFAOYSA-N
Popularity 0 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) 20.30 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.84
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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1-(1-Methyl-2-piperidyl)-2-butanone
2-Butanone, 1-(1-methyl-2-piperidyl)-
EL92020000

2D Structure

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2D Structure of 1-(1-Methyl-2-piperidyl)-2-butanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9652 96.52%
Caco-2 + 0.9450 94.50%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5778 57.78%
OATP2B1 inhibitior - 0.8455 84.55%
OATP1B1 inhibitior + 0.9529 95.29%
OATP1B3 inhibitior + 0.9462 94.62%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior + 0.5750 57.50%
BSEP inhibitior - 0.8909 89.09%
P-glycoprotein inhibitior - 0.9709 97.09%
P-glycoprotein substrate - 0.7527 75.27%
CYP3A4 substrate - 0.5838 58.38%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.5193 51.93%
CYP3A4 inhibition - 0.9841 98.41%
CYP2C9 inhibition - 0.9119 91.19%
CYP2C19 inhibition - 0.8358 83.58%
CYP2D6 inhibition - 0.8926 89.26%
CYP1A2 inhibition - 0.5544 55.44%
CYP2C8 inhibition - 0.9837 98.37%
CYP inhibitory promiscuity - 0.9720 97.20%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.7128 71.28%
Eye corrosion - 0.8907 89.07%
Eye irritation + 0.8594 85.94%
Skin irritation + 0.5090 50.90%
Skin corrosion + 0.6025 60.25%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5908 59.08%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.5028 50.28%
skin sensitisation - 0.8392 83.92%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity - 0.6071 60.71%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.8566 85.66%
Acute Oral Toxicity (c) III 0.7272 72.72%
Estrogen receptor binding - 0.9201 92.01%
Androgen receptor binding - 0.8627 86.27%
Thyroid receptor binding - 0.8264 82.64%
Glucocorticoid receptor binding - 0.9030 90.30%
Aromatase binding - 0.8207 82.07%
PPAR gamma - 0.8946 89.46%
Honey bee toxicity - 0.9807 98.07%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity - 0.7937 79.37%

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 98.37% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.64% 97.25%
CHEMBL4072 P07858 Cathepsin B 95.22% 93.67%
CHEMBL2581 P07339 Cathepsin D 92.31% 98.95%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.34% 93.04%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.68% 95.50%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 83.40% 95.17%
CHEMBL5203 P33316 dUTP pyrophosphatase 82.71% 99.18%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.23% 95.56%
CHEMBL5255 O00206 Toll-like receptor 4 81.30% 92.50%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 81.20% 97.50%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 81.15% 98.33%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.68% 93.00%

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.
Lobelia nummularia

Cross-Links

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PubChem 3027754
LOTUS LTS0004580
wikiData Q104963002