544710-36-3

Upstream product

• 303165-20-0 (+/-)-[3,4-bis(difluoromethoxy)phenyl]-(2-bromopyridin-5-yl)methanol 
• 624-28-2 2,5-dibromopyridine 

Downstream Products

• 1055709-47-1 3-{carbethoxy-2-[3,4-bis (difluoromethoxv)phenyl]-2-(2-bromo-5-pyridvl) ethyl} pyridine 
• 306760-68-9 4-{2-[3,4-Bis(difluoromethoxy)phenyl]-2-[6-(N-benzyl trifluoroacetamido)pyridin-3-yl]ethyl}pyridine 
• 306759-94-4 {5-[1-(3,4-Bis-difluoromethoxy-phenyl)-2-pyridin-4-yl-ethyl]-pyridin-2-yl}-((R)-1-phenyl-ethyl)-amine 
• 306759-92-2 4-{2-[3,4-Bis(difluoromethoxy)phenyl]-2-[6-(benzylamino)pyridin-3-yl]ethyl}pyridine 
• 303165-23-3 C₂₀H₁₅BrF₄N₂O₃ 
• 552287-62-4 (+/-)-4-{2-[3,4-bis(difluoromethoxy)phenyl]-2-[5-(2-carbomethoxy)pyridyl]ethyl}pyridine N-oxide 
• 552287-61-3 (+/-)-4-{2-[3,4-bis(difluoromethoxy)phenyl]-2-[5-(2-carbomethoxy)pyridyl]ethyl}pyridine 
• 544710-37-4 4-{1-Carbethoxy-2-[3,4-bis(difluoromethoxy)phenyl]-2-(6-bromo-pyridin-3-yl)ethyl}pyridine 

Relevant academic research and scientific papers

Substituted aminopyridines as potent and selective phosphodiesterase-4 inhibitors

The synthesis and the biological evaluation of new potent phosphodiesterase type 4 (PDE4) inhibitors are presented. This new series was elaborated by replacement of the metabolically resistant phenyl hexafluorocarbinol of L-791,943 (1) by a substituted aminopyridine residue. The structure-activity relationship of N-substitution on 3 led to the identification of (-)-3n which exhibited a good PDE4 inhibitor activity (HWB-TNFα=0.12 μM) and an improved pharmacokinetic profile over L-791,943 (rat t1/2=2 h). (-)-3n was well tolerated in ferret with an emetic threshold of 30 mg/kg (po) and was found to be active in the ovalbumin-induced bronchoconstriction model in guinea pig (54%, 0.1 mg/kg, ip) as well as the ascaris-induced bronchoconstriction model in sheep (64%/97%, early/late, 0.5 mg/kg, iv).

Optimization of a tertiary alcohol series of phosphodiesterase-4 (PDE4) inhibitors: Structure-activity relationship related to PDE4 inhibition and human ether-a-go-go related gene potassium channel binding affinity

A SAR study on the tertiary alcohol series of phosphodiesterase-4 (PDE4) inhibitors related to 1 is described. In addition to inhibitory potency against PDE4 and the lipopolysaccharide-induced production of TNFα in human whole blood, the binding affinity

HETEROSUBSTITUTED PYRIDINE DERIVATIVES AS PDE 4 INHIBITORS

The invention encompasses the novel compound of Formula I useful in the treatment of diseases, including asthma, by raising the level of cyclic adenosine-3',5'-monophosphate (cAMP) through the inhibition of phosphodiesterase IV (PDE 4)

Heterosubstituted pyridine derivatives as PDE4 inhibitors

The invention encompasses the novel compound of Formula I useful in the treatment of diseases, including asthma, by raising the level of cyclic adenosine-3′,5′-monophosphate (cAMP) through the inhibition of phosphodiesterase IV (PDE 4). or a pharmaceutically acceptable salt or hydrate thereof. The invention also encompasses pharmaceutical compositions and methods for treatment.