128830-76-2

Upstream product

• 367-25-9 2,4-difluorophenylamine 
• 1027938-12-0 4-(2-Chloro-phenyl)-3-isocyanato-6,8-dimethyl-quinoline 
• 59025-55-7 2,4-diflurophenylisocyanate 
• 128831-37-8 3-amino-4-(2-chlorophenyl)-6,8-dimethylquinoline 
• 128832-36-0 methyl 4-(2-chlorophenyl)-6,8-dimethyl-3-quinolinecarboxylate 
• 128832-45-1 4-(2-chlorophenyl)-6,8-dimethyl-3-quinolinecarboxamide 
• 128831-34-5 4-(2-chlorophenyl)-6,8-dimethyl-3-quinolinecarboxylic acid 

Downstream Products

• 128831-36-7 4-(2-chlorophenyl)-3-[3-(2,4-difluorophenyl)ureido]-6,8-dimethylquinoline 1-oxide 

Relevant academic research and scientific papers

Novel Acyl-CoA:Cholesterol Acyltransferase Inhibitors. Synthesis and Biological Activity of 3-Quinolylurea Derivatives

A series of 3-quinolylurea derivatives (1) was synthesized and evaluated for acyl-CoA:cholesterol acyltransferase (ACAT) inhibitory activity.For in vitro studies, the most potent inhibitory activity was found in derivatives having substituents at the 6,7-

Quinoline derivatives, their production and use

Quinoline derivatives of the formula: STR1 , wherein R is hydrogen, alkyl or aralkyl; m and n are 0 or 1, and each of rings A, B and C can have substituents, which are useful as inhibitors for acyl-CoA:Cholesterolacyltransferase.