Category: 253177-03-6

A new application about tert-Butyl 3-(iodomethyl)piperidine-1-carboxylate

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Application of 253177-03-6, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.253177-03-6, Name is tert-Butyl 3-(iodomethyl)piperidine-1-carboxylate, molecular formula is C11H20INO2. In a Article，once mentioned of 253177-03-6

A class of (E) and Q-3-styrylpiperidine derivatives was prepared as racemates and evaluated for affinity at sigma binding sites labeled with [3H]-(±-SKF-10,047. Some of these compounds exhibited high affinity and selectivity for sigma verus D1 and D2 binding sites.

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Reference：
Piperidine – Wikipedia,
Piperidine | C5H23582N – PubChem

 

Extracurricular laboratory:new discovery of 253177-03-6

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Reference of 253177-03-6, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.253177-03-6, Name is tert-Butyl 3-(iodomethyl)piperidine-1-carboxylate, molecular formula is C11H20INO2. In a Patent，once mentioned of 253177-03-6

One aspect of the present invention relates to novel heterocyclic compounds. A second aspect of the present invention relates to the use of the novel heterocyclic compounds as ligands for various cellular receptors, including opiate receptors, other G-protein-coupled receptors, and ion channels. An additional aspect of the present invention relates to the use of the novel heterocyclic compounds as analgesics.

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Reference：
Piperidine – Wikipedia,
Piperidine | C5H23578N – PubChem

 

Extended knowledge of 253177-03-6

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 253177-03-6

Electric Literature of 253177-03-6, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.253177-03-6, Name is tert-Butyl 3-(iodomethyl)piperidine-1-carboxylate, molecular formula is C11H20INO2. In a Patent，once mentioned of 253177-03-6

One aspect of the present invention relates to novel heterocyclic compounds. A second aspect of the present invention relates to the use of the novel heterocyclic compounds as ligands for various cellular receptors, including opiate receptors, other G-protein-coupled receptors, and ion channels. An additional aspect of the present invention relates to the use of the novel heterocyclic compounds as analgesics.

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Reference：
Piperidine – Wikipedia,
Piperidine | C5H23577N – PubChem

 

Simple exploration of 253177-03-6

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.253177-03-6. In my other articles, you can also check out more blogs about 253177-03-6

Reference of 253177-03-6, In heterogeneous catalysis, the catalyst is in a different phase from the reactants. At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 253177-03-6, name is tert-Butyl 3-(iodomethyl)piperidine-1-carboxylate. In an article，Which mentioned a new discovery about 253177-03-6

The present invention relates to O-GlcNAc hydrolase (OGA) inhibitors. The invention is also directed to pharmaceutical compositions comprising such compounds, to processes for preparing such compounds and compositions, and to the use of such compounds and compositions for the prevention and treatment of disorders in which inhibition of OGA is beneficial, such as tauopathies, in particular Alzheimer’s disease or progressive supranuclear palsy; and neurodegenerative diseases accompanied by a tau pathology, in particular amyotrophic lateral sclerosis or frontotemporal lobe dementia caused by C9ORF72 mutations.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.253177-03-6. In my other articles, you can also check out more blogs about 253177-03-6

Reference：
Piperidine – Wikipedia,
Piperidine | C5H23572N – PubChem