1-Piperidin-1-yloctadecane-1,12-dione

Details

Top
Internal ID bd7f7f6c-48cc-43bc-8763-fccedad6c2c8
Taxonomy Organoheterocyclic compounds > Piperidines > N-acylpiperidines
IUPAC Name 1-piperidin-1-yloctadecane-1,12-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H43NO2/c1-2-3-4-12-17-22(25)18-13-9-7-5-6-8-10-14-19-23(26)24-20-15-11-16-21-24/h2-21H2,1H3
InChI Key YTGCTUPAVSDGRB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C23H43NO2
Molecular Weight 365.60 g/mol
Exact Mass 365.329379614 g/mol
Topological Polar Surface Area (TPSA) 37.40 Ų
XlogP 6.60
Atomic LogP (AlogP) 6.44
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 16

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 1-Piperidin-1-yloctadecane-1,12-dione

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9783 97.83%
Caco-2 + 0.5065 50.65%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.4690 46.90%
OATP2B1 inhibitior - 0.8532 85.32%
OATP1B1 inhibitior + 0.9469 94.69%
OATP1B3 inhibitior + 0.9460 94.60%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.7263 72.63%
P-glycoprotein inhibitior - 0.7172 71.72%
P-glycoprotein substrate - 0.7577 75.77%
CYP3A4 substrate - 0.6065 60.65%
CYP2C9 substrate - 0.8197 81.97%
CYP2D6 substrate - 0.8415 84.15%
CYP3A4 inhibition - 0.9666 96.66%
CYP2C9 inhibition - 0.7653 76.53%
CYP2C19 inhibition + 0.5417 54.17%
CYP2D6 inhibition - 0.9483 94.83%
CYP1A2 inhibition - 0.6206 62.06%
CYP2C8 inhibition - 0.9477 94.77%
CYP inhibitory promiscuity - 0.8714 87.14%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5999 59.99%
Eye corrosion - 0.9490 94.90%
Eye irritation + 0.8405 84.05%
Skin irritation - 0.6038 60.38%
Skin corrosion - 0.6799 67.99%
Ames mutagenesis - 0.9600 96.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6074 60.74%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.7148 71.48%
skin sensitisation - 0.9039 90.39%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6368 63.68%
Acute Oral Toxicity (c) III 0.7369 73.69%
Estrogen receptor binding - 0.6604 66.04%
Androgen receptor binding - 0.5894 58.94%
Thyroid receptor binding - 0.6064 60.64%
Glucocorticoid receptor binding - 0.7381 73.81%
Aromatase binding - 0.7271 72.71%
PPAR gamma - 0.6371 63.71%
Honey bee toxicity - 0.9929 99.29%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity + 0.7823 78.23%
Fish aquatic toxicity - 0.8342 83.42%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.61% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.39% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 96.53% 89.63%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 95.20% 91.81%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 92.14% 92.86%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 88.29% 95.17%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 88.21% 100.00%
CHEMBL3105 P09874 Poly [ADP-ribose] polymerase-1 87.77% 93.90%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.67% 99.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.22% 97.25%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.84% 92.08%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 85.40% 90.24%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 85.35% 95.50%
CHEMBL1744525 P43490 Nicotinamide phosphoribosyltransferase 85.08% 96.25%
CHEMBL4040 P28482 MAP kinase ERK2 83.96% 83.82%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.57% 90.71%
CHEMBL5255 O00206 Toll-like receptor 4 82.03% 92.50%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.83% 93.56%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.89% 94.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.45% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.29% 86.33%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 80.23% 97.50%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.01% 96.61%

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.
Achillea lycaonica

Cross-Links

Top
PubChem 86021954
LOTUS LTS0017134
wikiData Q105361390