94592-63-9

Upstream product

• 98-88-4 benzoyl chloride 
• 98421-16-0 5-(2-aminoethyl)-8-methoxyquinoline 
• 94592-57-1 5-(cyanomethyl)-8-methoxyquinoline 
• 57434-83-0 2-(8-hydroxyquinolin-5-yl)acetonitrile 

Downstream Products

• 94592-64-0 5-(2-benzamidoethyl)-8-methoxyquinoline N-oxide 
• 94592-65-1 5-(2-benzamidoethyl)-8-methoxycarbostyril 
• 94592-40-2 5-<2-<<2-(4-methoxyphenyl)ethyl>amino>ethyl>-8-methoxycarbostyril 
• 94592-41-3 8-methoxy-5-<2-<<2-(4-hydroxyphenyl)ethyl>-n-propylamino>ethyl>carbostyril 
• 94592-39-9 5-<2-<<2-(4-methoxyphenyl)-2-hydroxyethyl>amino>ethyl>-8-methoxycarbostyril 
• 98421-22-8 5-<2-<<2-(4-methoxyphenyl)-2-hydroxy-1-cyanoethyl>amino>ethyl>-8-methoxycarbostyril 
• 94592-43-5 8-hydroxy-5-<2-<<2-(4-hydroxyphenyl)ethyl>amino>ethyl>carbostyril hydrobromide 
• 94938-81-5 5-<2-(benzylamino)ethyl>-8-methoxycarbostyril 
• 94592-42-4 8-hydroxy-5-<2-<<2-(4-hydroxyphenyl)ethyl>-n-propylamino>ethyl>carbostyril 

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