1-Piperidin-1-ylicosa-2,4,14-trien-1-one

Details

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Internal ID c7de589d-064c-47cd-a9aa-ff5a639ae06c
Taxonomy Organoheterocyclic compounds > Piperidines > N-acylpiperidines
IUPAC Name 1-piperidin-1-ylicosa-2,4,14-trien-1-one
SMILES (Canonical) CCCCCC=CCCCCCCCCC=CC=CC(=O)N1CCCCC1
SMILES (Isomeric) CCCCCC=CCCCCCCCCC=CC=CC(=O)N1CCCCC1
InChI InChI=1S/C25H43NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-19-22-25(27)26-23-20-18-21-24-26/h6-7,16-17,19,22H,2-5,8-15,18,20-21,23-24H2,1H3
InChI Key XZJZLXUTPLOJRS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H43NO
Molecular Weight 373.60 g/mol
Exact Mass 373.334464995 g/mol
Topological Polar Surface Area (TPSA) 20.30 Ų
XlogP 8.60
Atomic LogP (AlogP) 7.37
H-Bond Acceptor 1
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-ylicosa-2,4,14-trien-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9840 98.40%
Caco-2 - 0.6547 65.47%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Plasma membrane 0.5341 53.41%
OATP2B1 inhibitior - 0.8574 85.74%
OATP1B1 inhibitior + 0.8958 89.58%
OATP1B3 inhibitior + 0.9452 94.52%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior + 0.7752 77.52%
P-glycoprotein inhibitior - 0.6060 60.60%
P-glycoprotein substrate - 0.7798 77.98%
CYP3A4 substrate - 0.5374 53.74%
CYP2C9 substrate + 0.5844 58.44%
CYP2D6 substrate - 0.8890 88.90%
CYP3A4 inhibition - 0.9826 98.26%
CYP2C9 inhibition - 0.8229 82.29%
CYP2C19 inhibition - 0.5270 52.70%
CYP2D6 inhibition - 0.9250 92.50%
CYP1A2 inhibition - 0.5259 52.59%
CYP2C8 inhibition - 0.8864 88.64%
CYP inhibitory promiscuity - 0.8560 85.60%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5866 58.66%
Eye corrosion - 0.8390 83.90%
Eye irritation - 0.5000 50.00%
Skin irritation + 0.6115 61.15%
Skin corrosion - 0.5115 51.15%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7148 71.48%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.5460 54.60%
skin sensitisation - 0.8514 85.14%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.7146 71.46%
Acute Oral Toxicity (c) III 0.7267 72.67%
Estrogen receptor binding + 0.6447 64.47%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding + 0.5498 54.98%
Glucocorticoid receptor binding - 0.4691 46.91%
Aromatase binding - 0.6439 64.39%
PPAR gamma + 0.5982 59.82%
Honey bee toxicity - 0.9897 98.97%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.8340 83.40%
Fish aquatic toxicity - 0.4121 41.21%

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 98.56% 89.63%
CHEMBL2581 P07339 Cathepsin D 96.26% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.23% 96.09%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 94.81% 91.81%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 93.69% 92.86%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.49% 99.17%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 89.66% 100.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.04% 92.08%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 85.21% 95.50%
CHEMBL1781 P11387 DNA topoisomerase I 84.95% 97.00%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 83.57% 95.27%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.70% 94.33%
CHEMBL3105 P09874 Poly [ADP-ribose] polymerase-1 81.83% 93.90%
CHEMBL1744525 P43490 Nicotinamide phosphoribosyltransferase 81.81% 96.25%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 81.15% 83.57%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 81.01% 90.24%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.26% 93.56%

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.
Piper retrofractum

Cross-Links

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PubChem 75184729
LOTUS LTS0200698
wikiData Q105344987