(2E,9E)-1-piperidin-1-ylpentadeca-2,9-dien-12,14-diyn-1-one

Details

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Internal ID 77a3c44f-8f86-441a-bae6-6bfc07c15cdd
Taxonomy Organoheterocyclic compounds > Piperidines > N-acylpiperidines
IUPAC Name (2E,9E)-1-piperidin-1-ylpentadeca-2,9-dien-12,14-diyn-1-one
SMILES (Canonical) C#CC#CCC=CCCCCCC=CC(=O)N1CCCCC1
SMILES (Isomeric) C#CC#CC/C=C/CCCCC/C=C/C(=O)N1CCCCC1
InChI InChI=1S/C20H27NO/c1-2-3-4-5-6-7-8-9-10-11-12-14-17-20(22)21-18-15-13-16-19-21/h1,6-7,14,17H,5,8-13,15-16,18-19H2/b7-6+,17-14+
InChI Key TVXTTXCVKUFWRM-PDCGFXJVSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H27NO
Molecular Weight 297.40 g/mol
Exact Mass 297.209264485 g/mol
Topological Polar Surface Area (TPSA) 20.30 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.09
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2E,9E)-1-piperidin-1-ylpentadeca-2,9-dien-12,14-diyn-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 + 0.9643 96.43%
Caco-2 + 0.6221 62.21%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.5234 52.34%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.9140 91.40%
OATP1B3 inhibitior + 0.9498 94.98%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior + 0.6500 65.00%
BSEP inhibitior - 0.4600 46.00%
P-glycoprotein inhibitior - 0.7636 76.36%
P-glycoprotein substrate - 0.8157 81.57%
CYP3A4 substrate + 0.5152 51.52%
CYP2C9 substrate - 0.6128 61.28%
CYP2D6 substrate - 0.8647 86.47%
CYP3A4 inhibition - 0.9356 93.56%
CYP2C9 inhibition - 0.7795 77.95%
CYP2C19 inhibition + 0.6071 60.71%
CYP2D6 inhibition - 0.9236 92.36%
CYP1A2 inhibition - 0.6260 62.60%
CYP2C8 inhibition - 0.7942 79.42%
CYP inhibitory promiscuity - 0.6690 66.90%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.5033 50.33%
Eye corrosion - 0.8547 85.47%
Eye irritation - 0.8166 81.66%
Skin irritation + 0.6693 66.93%
Skin corrosion - 0.6658 66.58%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7024 70.24%
Micronuclear - 0.7500 75.00%
Hepatotoxicity - 0.5592 55.92%
skin sensitisation - 0.8625 86.25%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.7599 75.99%
Acute Oral Toxicity (c) III 0.5824 58.24%
Estrogen receptor binding - 0.5119 51.19%
Androgen receptor binding - 0.6500 65.00%
Thyroid receptor binding - 0.5998 59.98%
Glucocorticoid receptor binding - 0.6306 63.06%
Aromatase binding - 0.5466 54.66%
PPAR gamma + 0.6921 69.21%
Honey bee toxicity - 0.9380 93.80%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.6924 69.24%
Fish aquatic toxicity - 0.8291 82.91%

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
CHEMBL230 P35354 Cyclooxygenase-2 96.73% 89.63%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.83% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.53% 98.95%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 89.84% 83.57%
CHEMBL3105 P09874 Poly [ADP-ribose] polymerase-1 88.58% 93.90%
CHEMBL1744525 P43490 Nicotinamide phosphoribosyltransferase 87.26% 96.25%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.88% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 83.21% 90.17%
CHEMBL1781 P11387 DNA topoisomerase I 81.52% 97.00%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 81.03% 97.34%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.74% 100.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.67% 95.50%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 80.42% 90.24%

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 13846797
LOTUS LTS0064605
wikiData Q105265616