1-Piperidin-1-yloctadec-2-ene-1,12-dione

Details

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Internal ID 1a415c22-9e85-45ce-8586-10197cbea3d9
Taxonomy Organoheterocyclic compounds > Piperidines > N-acylpiperidines
IUPAC Name 1-piperidin-1-yloctadec-2-ene-1,12-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H41NO2/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/h14,19H,2-13,15-18,20-21H2,1H3
InChI Key GRKRIZFIWHHTAJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H41NO2
Molecular Weight 363.60 g/mol
Exact Mass 363.313729551 g/mol
Topological Polar Surface Area (TPSA) 37.40 Ų
XlogP 6.50
Atomic LogP (AlogP) 6.22
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 15

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Piperidin-1-yloctadec-2-ene-1,12-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9831 98.31%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Plasma membrane 0.5655 56.55%
OATP2B1 inhibitior - 0.8558 85.58%
OATP1B1 inhibitior + 0.8872 88.72%
OATP1B3 inhibitior + 0.9433 94.33%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.7674 76.74%
P-glycoprotein inhibitior - 0.5772 57.72%
P-glycoprotein substrate - 0.7541 75.41%
CYP3A4 substrate - 0.5363 53.63%
CYP2C9 substrate - 0.8052 80.52%
CYP2D6 substrate - 0.8860 88.60%
CYP3A4 inhibition - 0.9504 95.04%
CYP2C9 inhibition - 0.7547 75.47%
CYP2C19 inhibition + 0.5625 56.25%
CYP2D6 inhibition - 0.9528 95.28%
CYP1A2 inhibition - 0.5849 58.49%
CYP2C8 inhibition - 0.8625 86.25%
CYP inhibitory promiscuity - 0.8215 82.15%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.5746 57.46%
Eye corrosion - 0.9550 95.50%
Eye irritation + 0.6187 61.87%
Skin irritation - 0.5667 56.67%
Skin corrosion - 0.6850 68.50%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4188 41.88%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.5908 59.08%
skin sensitisation - 0.8815 88.15%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.8011 80.11%
Acute Oral Toxicity (c) III 0.7095 70.95%
Estrogen receptor binding + 0.5733 57.33%
Androgen receptor binding - 0.5931 59.31%
Thyroid receptor binding + 0.5248 52.48%
Glucocorticoid receptor binding - 0.5738 57.38%
Aromatase binding - 0.7515 75.15%
PPAR gamma + 0.6851 68.51%
Honey bee toxicity - 0.9834 98.34%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity + 0.8578 85.78%
Fish aquatic toxicity - 0.6640 66.40%

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
CHEMBL230 P35354 Cyclooxygenase-2 98.70% 89.63%
CHEMBL2581 P07339 Cathepsin D 97.21% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.18% 96.09%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 94.78% 91.81%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.22% 99.17%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 90.62% 92.86%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 90.41% 92.08%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 89.18% 100.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 86.68% 95.50%
CHEMBL1781 P11387 DNA topoisomerase I 86.31% 97.00%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 84.07% 95.17%
CHEMBL3105 P09874 Poly [ADP-ribose] polymerase-1 83.79% 93.90%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.77% 94.33%
CHEMBL1744525 P43490 Nicotinamide phosphoribosyltransferase 83.68% 96.25%
CHEMBL4588 P22894 Matrix metalloproteinase 8 83.25% 94.66%
CHEMBL5255 O00206 Toll-like receptor 4 83.15% 92.50%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 82.47% 90.24%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 81.39% 97.50%

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.
Achillea lycaonica

Cross-Links

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PubChem 163000737
LOTUS LTS0104238
wikiData Q105016139