Nom du produit:1-{[1-(3-ethylphenyl)-1H-1,2,3-triazol-4-yl]carbonyl}piperidin-4-amine

IUPAC Name:1-[1-(3-ethylphenyl)-1H-1,2,3-triazole-4-carbonyl]piperidin-4-amine

CAS:1351788-36-7
Formule moléculaire:C16H21N5O
Pureté:97%
Numéro de catalogue:CM495031
Poids moléculaire:299.38

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CM495031-1g 1-2 Weeks ƿǶǑ

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Détails du produit

N° CAS:1351788-36-7
Formule moléculaire:C16H21N5O
Point de fusion:-
Code SMILES:O=C(N1CCC(N)CC1)C2=CN(C3=CC=CC(CC)=C3)N=N2
Densité:
Numéro de catalogue:CM495031
Poids moléculaire:299.38
Point d'ébullition:
N° Mdl:
Stockage:

Category Infos

Piperidines
Piperidine is an azacycloalkane that is cyclohexane in which one of the carbons is replaced by a nitrogen. Although piperidine is a common organic compound, it is an immensely important class of compounds medicinally: the piperidine ring is the most common heterocyclic subunit among FDA approved drugs.
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Triazoles
Triazole refers to a heterocyclic compound with the molecular formula C2H3N3, which has a five-membered ring consisting of two carbon atoms and three nitrogen atoms. Neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease already affect many people around the world, and these numbers are increasing rapidly. Treatment for these disorders is often aimed at relieving symptoms and has no cure. Research on new molecules is underway, and heterocyclic compounds have important pharmacological implications. Triazoles and tetrazoles are emerging as new molecules in this field.

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Product Overview 1-{[1-(3-ethylphenyl)-1H-1,2,3-triazol-4-yl]carbonyl}piperidin-4-amine, also known as EPTP, is a chemical compound that has gained significant attention in the field of scientific research. This compound belongs to the class of piperidines and is a triazole-based inhibitor of the protein kinase B (PKB/Akt) signaling pathway.
Synthesis and Application The synthesis of 1-{[1-(3-ethylphenyl)-1H-1,2,3-triazol-4-yl]carbonyl}piperidin-4-amine involves the reaction of 4-aminopiperidine with 3-ethylphenylisocyanate and 1H-1,2,3-triazole-4-carboxylic acid in the presence of a coupling agent such as N,N'-diisopropylcarbodiimide (DIC) or N,N'-dicyclohexylcarbodiimide (DCC). The reaction is carried out in a suitable solvent such as dimethylformamide (DMF) or dimethyl sulfoxide (DMSO) at room temperature, and the product is obtained after purification by column chromatography. 1-{[1-(3-ethylphenyl)-1H-1,2,3-triazol-4-yl]carbonyl}piperidin-4-amine has been extensively studied for its potential therapeutic applications in various diseases, including cancer, diabetes, and neurodegenerative disorders. It has been found to inhibit the activity of PKB/Akt, a key signaling pathway that plays a critical role in cell survival, proliferation, and metabolism. Inhibition of this pathway has been shown to induce apoptosis (programmed cell death) and suppress tumor growth in various cancer cell lines. 1-{[1-(3-ethylphenyl)-1H-1,2,3-triazol-4-yl]carbonyl}piperidin-4-amine has also been found to improve glucose metabolism and insulin sensitivity in diabetic animal models. Furthermore, it has been shown to protect against neuronal damage and cognitive impairment in neurodegenerative disease models.
Future Directions Future directions for 1-{[1-(3-ethylphenyl)-1H-1,2,3-triazol-4-yl]carbonyl}piperidin-4-amine research include the development of more potent and selective analogs, optimization of its pharmacokinetic properties, and evaluation of its efficacy and safety in human clinical trials. Furthermore, the potential use of 1-{[1-(3-ethylphenyl)-1H-1,2,3-triazol-4-yl]carbonyl}piperidin-4-amine as a combination therapy with other anticancer agents or as a radiosensitizer in cancer treatment is an area of active investigation. Additionally, the role of 1-{[1-(3-ethylphenyl)-1H-1,2,3-triazol-4-yl]carbonyl}piperidin-4-amine in other diseases, such as cardiovascular and inflammatory disorders, warrants further investigation.