1364677-88-2

Usage

Molecular Structure

2-(4-chlorophenyl)-3-(cyclopropylmethoxy)pyridine is a pyridine derivative with a 4-chlorophenyl group and a cyclopropylmethoxy group attached to the pyridine ring.

Usage

The compound can be used for research and development purposes, and has potential applications in the pharmaceutical industry for the development of new drugs, particularly in the field of neuroscience and central nervous system disorders.

Building Block

The compound may also be used as a building block in organic synthesis for the creation of other complex compounds.

Agrochemical Applications

2-(4-chlorophenyl)-3-(cyclopropylmethoxy)pyridine may have some potential in agrochemical applications, although further research would be necessary to fully understand its potential uses in this industry.

Upstream product

• 2516-33-8 Cyclopropylmethanol 
• 1233702-02-7 2-(4-chlorophenyl)-3-fluoropyridine 
• 17282-04-1 2-chloro-3-fluoropyridine 
• 1679-18-1 4-Chlorophenylboronic acid 

Relevant academic research and scientific papers

6-alkoxy-5-aryl-3-pyridinecarboxamides, a new series of bioavailable cannabinoid receptor type 1 (CB1) antagonists including peripherally selective compounds

We identified 6-alkoxy-5-aryl-3-pyridinecarboxamides as potent CB1 receptor antagonists with high selectivity over CB2 receptors. The series was optimized to reduce lipophilicity compared to rimonabant to achieve peripherally active molecules with minimal central effects. Several compounds that showed high plasma exposures in rats were evaluated in vivo to probe the contribution of central vs peripheral CB1 agonism to metabolic improvement. Both rimonabant and 14g, a potent brain penetrant CB1 receptor antagonist, significantly reduced the rate of body weight gain. However, 14h, a molecule with markedly reduced brain exposure, had no significant effect on body weight. PK studies confirmed similarly high exposure of both 14h and 14g in the periphery but 10-fold lower exposure in the brain for 14h. On the basis of these data, which are consistent with reported effects in tissue-specific CB1 receptor KO mice, we conclude that the metabolic benefits of CB1 receptor antagonists are primarily centrally mediated as originally believed.

HETEROARYLMETHYL AMIDES

The present invention relates to compounds of the formula wherein A1, A2, A3 and R1 to R8 are defined in the description, and to pharmaceutically acceptable salts thereof, their manufacture, pharmaceutical compositions containing them and their use as medicaments for the treatment and/or prophylaxis of diseases which can be treated with HDL-cholesterol raising agents, such as particularly dyslipidemia, atherosclerosis and cardiovascular diseases.

HETEROARYLMETHYL AMIDES

The present invention relates to compounds of the formula I wherein A1, A2, A3 and R1 to R8 are defined in the description, and to pharmaceutically acceptable salts thereof, their manufacture, pharmaceutical compositions containing them and their use as medicaments for the treatment and/or prophylaxis of diseases which can be treated with HDL-cholesterol raising agents, such as particularly dyslipidemia, atherosclerosis and cardiovascular diseases.