1-Piperidin-1-yltetradeca-2,4,6,10-tetraen-8-yn-1-one

Details

Top
Internal ID 33707074-9f10-4be3-a070-75c8b44e5001
Taxonomy Organoheterocyclic compounds > Piperidines > N-acylpiperidines
IUPAC Name 1-piperidin-1-yltetradeca-2,4,6,10-tetraen-8-yn-1-one
SMILES (Canonical) CCCC=CC#CC=CC=CC=CC(=O)N1CCCCC1
SMILES (Isomeric) CCCC=CC#CC=CC=CC=CC(=O)N1CCCCC1
InChI InChI=1S/C19H25NO/c1-2-3-4-5-6-7-8-9-10-11-13-16-19(21)20-17-14-12-15-18-20/h4-5,8-11,13,16H,2-3,12,14-15,17-18H2,1H3
InChI Key FXMWOIBPXOJROS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C19H25NO
Molecular Weight 283.40 g/mol
Exact Mass 283.193614421 g/mol
Topological Polar Surface Area (TPSA) 20.30 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.03
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 1-Piperidin-1-yltetradeca-2,4,6,10-tetraen-8-yn-1-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9808 98.08%
Caco-2 + 0.8025 80.25%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Plasma membrane 0.5058 50.58%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9103 91.03%
OATP1B3 inhibitior + 0.9474 94.74%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior - 0.6018 60.18%
P-glycoprotein inhibitior - 0.7731 77.31%
P-glycoprotein substrate - 0.7928 79.28%
CYP3A4 substrate - 0.5165 51.65%
CYP2C9 substrate - 0.6083 60.83%
CYP2D6 substrate - 0.8821 88.21%
CYP3A4 inhibition - 0.9539 95.39%
CYP2C9 inhibition - 0.7639 76.39%
CYP2C19 inhibition - 0.5142 51.42%
CYP2D6 inhibition - 0.9329 93.29%
CYP1A2 inhibition - 0.6219 62.19%
CYP2C8 inhibition - 0.8933 89.33%
CYP inhibitory promiscuity - 0.7096 70.96%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.5563 55.63%
Eye corrosion - 0.9073 90.73%
Eye irritation - 0.6801 68.01%
Skin irritation + 0.5820 58.20%
Skin corrosion - 0.6721 67.21%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6478 64.78%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.6306 63.06%
skin sensitisation - 0.8429 84.29%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.5960 59.60%
Acute Oral Toxicity (c) III 0.5580 55.80%
Estrogen receptor binding - 0.5344 53.44%
Androgen receptor binding - 0.6419 64.19%
Thyroid receptor binding + 0.6331 63.31%
Glucocorticoid receptor binding - 0.5898 58.98%
Aromatase binding + 0.6722 67.22%
PPAR gamma - 0.6184 61.84%
Honey bee toxicity - 0.9440 94.40%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity - 0.5758 57.58%

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 95.44% 96.09%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 94.30% 83.57%
CHEMBL230 P35354 Cyclooxygenase-2 89.86% 89.63%
CHEMBL2581 P07339 Cathepsin D 89.69% 98.95%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 84.14% 96.38%
CHEMBL218 P21554 Cannabinoid CB1 receptor 82.96% 96.61%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.66% 94.33%
CHEMBL221 P23219 Cyclooxygenase-1 81.10% 90.17%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.82% 95.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.47% 86.33%

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 ligustica

Cross-Links

Top
PubChem 162891167
LOTUS LTS0137612
wikiData Q105004074