94592-43-5

Upstream product

• 94592-65-1 5-(2-benzamidoethyl)-8-methoxycarbostyril 
• 98421-22-8 5-<2-<<2-(4-methoxyphenyl)-2-hydroxy-1-cyanoethyl>amino>ethyl>-8-methoxycarbostyril 
• 94592-39-9 5-<2-<<2-(4-methoxyphenyl)-2-hydroxyethyl>amino>ethyl>-8-methoxycarbostyril 
• 94592-64-0 5-(2-benzamidoethyl)-8-methoxyquinoline N-oxide 
• 94592-63-9 5-(2-benzamidoethyl)-8-methoxyquinoline 
• 94592-66-2 5-(2-aminoethyl)-8-methoxycarbostyril 
• 94592-57-1 5-(cyanomethyl)-8-methoxyquinoline 
• 98421-16-0 5-(2-aminoethyl)-8-methoxyquinoline 
• 123-11-5 4-methoxy-benzaldehyde 
• 57434-83-0 2-(8-hydroxyquinolin-5-yl)acetonitrile 
• 81860-68-6 3-(4-methoxyphenyl)-oxiranecarbonitrile 
• 94592-40-2 5-<2-<<2-(4-methoxyphenyl)ethyl>amino>ethyl>-8-methoxycarbostyril 

Relevant academic research and scientific papers

Dopamine Receptor Agonist Activity of Some 5-(2-Aminoethyl)carbostyril Derivatives

The potency of β-adrenoreceptor agonists, e.g.,isoproterenol, is strikingly increased by substitution of the meta catecholic hydroxyl group with the NH group of a carbostyril system.To explore the possibility that comparable potency enhacement might occur