1-(Piperidin-1-yl)undeca-2,4-diene-8,10-diyn-1-one

Details

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Internal ID 74f8efd6-2c56-441a-af7a-38605c69e1c8
Taxonomy Organoheterocyclic compounds > Piperidines > N-acylpiperidines
IUPAC Name 1-piperidin-1-ylundeca-2,4-dien-8,10-diyn-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H19NO/c1-2-3-4-5-6-7-8-10-13-16(18)17-14-11-9-12-15-17/h1,7-8,10,13H,5-6,9,11-12,14-15H2
InChI Key JGKXLHHRMGZICC-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H19NO
Molecular Weight 241.33 g/mol
Exact Mass 241.146664230 g/mol
Topological Polar Surface Area (TPSA) 20.30 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.53
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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1-(Piperidin-1-yl)undeca-2,4-diene-8,10-diyn-1-one
DTXSID10761574

2D Structure

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2D Structure of 1-(Piperidin-1-yl)undeca-2,4-diene-8,10-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 + 0.9051 90.51%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.5234 52.34%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9370 93.70%
OATP1B3 inhibitior + 0.9498 94.98%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior + 0.6500 65.00%
BSEP inhibitior - 0.7709 77.09%
P-glycoprotein inhibitior - 0.9737 97.37%
P-glycoprotein substrate - 0.8882 88.82%
CYP3A4 substrate - 0.5315 53.15%
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 - 0.8822 88.22%
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 + 0.5278 52.78%
Skin irritation + 0.6693 66.93%
Skin corrosion - 0.6658 66.58%
Ames mutagenesis - 0.6878 68.78%
Human Ether-a-go-go-Related Gene inhibition - 0.5240 52.40%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.8625 86.25%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.5573 55.73%
Acute Oral Toxicity (c) III 0.5824 58.24%
Estrogen receptor binding - 0.6425 64.25%
Androgen receptor binding - 0.5943 59.43%
Thyroid receptor binding - 0.5593 55.93%
Glucocorticoid receptor binding - 0.5484 54.84%
Aromatase binding - 0.5906 59.06%
PPAR gamma + 0.5182 51.82%
Honey bee toxicity - 0.9309 93.09%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6000 60.00%
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 97.83% 89.63%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 93.18% 83.57%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.17% 96.09%
CHEMBL3105 P09874 Poly [ADP-ribose] polymerase-1 90.29% 93.90%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 88.25% 97.34%
CHEMBL221 P23219 Cyclooxygenase-1 84.75% 90.17%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 83.92% 98.75%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.72% 85.14%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 82.38% 97.47%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 81.10% 90.24%
CHEMBL1744525 P43490 Nicotinamide phosphoribosyltransferase 80.96% 96.25%
CHEMBL3650 P11362 Fibroblast growth factor receptor 1 80.03% 98.47%

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 falcata
Artemisia dracunculus

Cross-Links

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PubChem 71333288
LOTUS LTS0194552
wikiData Q82716474