292859-75-7

Upstream product

• 120-57-0 piperonal 
• 292859-76-8 1-(2-aminophenyl)-3-(4-methoxyphenyl)propan-1-one 
• 74599-23-8 4-methoxy-2'-nitro-chalcone 

Downstream Products

• 292859-74-6 N-benzo[1,3]dioxol-5-ylmethyl-N-{2-[3-(4-methoxy-phenyl)-propionyl]-phenyl}-oxalamic acid ethyl ester 
• 184241-88-1 1-benzo[1,3]dioxol-5-ylmethyl-3-(4-methoxy-benzyl)-4-oxo-1,4-dihydro-quinoline-2-carboxylic acid ethyl ester 

Relevant academic research and scientific papers

1,3-disubstituted-2-carboxyl quinolones: Highly potent and selective endothelin A receptor antagonists

The design, synthesis, and in vitro biological activity of a series of 2-carboxy quinolone antagonists selective for the endothelin A receptor are presented. Introduction of a second acid group in position 3 of the quinolone ring increases dramatically the selectivity for ET(A). (C) 2000 Elsevier Science Ltd. All rights reserved.