773013-64-2

Upstream product

• 10420-97-0 1-(4-methoxyphenyl)-2-(pyridin-2-yl)ethanone 

Downstream Products

• 881383-39-7 1-(4-methoxyphenyl)-2-(3-methoxyphenyl)amino-2-(pyridin-2-yl)ethanone 
• 881383-38-6 1-(4-methoxyphenyl)-2-phenylamino-2-(pyridin-2-yl)ethanone 
• 881383-42-2 1-(4-methoxyphenyl)-2-[N-(3-methoxyphenyl)-N-methylamino]-2-(pyridin-2-yl)ethanone 
• 881383-41-1 1-(4-methoxyphenyl)-2-(N-ethyl-N-phenylamino)-2-(pyridin-2-yl)ethanone 
• 881383-40-0 1-(4-methoxyphenyl)-2-(N-methyl-N-phenylamino)-2-(pyridin-2-yl)ethanone 
• 881383-48-8 1-ethyl-6-methoxy-3-(4-methoxyphenyl)-2-(pyridin-2-yl)-1H-indole 
• 881383-47-7 6-methoxy-3-(4-methoxyphenyl)-1-methyl-2-(pyridin-2-yl)-1H-indole 
• 881383-46-6 1-ethyl-3-(4-methoxyphenyl)-2-(pyridin-2-yl)-1H-indole 
• 881383-45-5 3-(4-methoxyphenyl)-1-methyl-2-(pyridin-2-yl)-1H-indole 
• 881383-44-4 3-(4-methoxyphenyl)-2-(pyridin-2-yl)-1H-indole 
• 881383-43-3 1-(4-methoxyphenyl)-2-[N-(3-methoxyphenyl)-N-ethylamino]-2-(pyridin-2-yl)ethanone 

Relevant academic research and scientific papers

2-Pyridin-2-yl-1H-indole derivatives: Synthesis, estrogen receptor binding affinity, and photophysical properties

A series of novel 2-pyridin-2-yl-1H-indole derivatives (4a-f) was prepared by intramolecular cyclodehydration of α-anilinyl (or 3-anisidyl)-2- pyridin-2-yl-ethanones (2a-f) and their optical spectroscopy and estrogen receptor (ER) binding properties were

5-pyridyl-1,3-thiazole derivatives

Novel compounds of the formula: STR1 wherein R1 stands for an optionally substituted alkyl group, alkenyl group, aryl group, aralkyl group, cycloalkyl group, heterocyclic group having carbon as the bonding hand or amino group, R2 stands for a pyridyl group which may be substituted with alkyl group, and R3 stands for an optionally substituted aryl group or salts thereof, have analgesic, anti-piretic, anti-inflammatory and anti-ulcer actions, and can be administered to mammals for the therapy of pain, inflammatory diseases, rheumatic chronic diseases.