18830-58-5

Upstream product

• 118-48-9 isatoic anhydride 
• 937026-49-8 6-amino-1,3-dimethyl-5-(2-nitrobenzylideneamino)uracil 
• 78146-60-8 8-(o-Nitrophenyl)theophylline 
• 18830-59-6 6-amino-1,3-dimethyl-5-(2-aminobenzamido)uracil 
• 552-89-6 2-nitro-benzaldehyde 
• 5440-00-6 4,5-Diamino-1,3-dimethyluracil 

Relevant academic research and scientific papers

Inhibition of monoamine oxidase B by selected benzimidazole and caffeine analogues

We have recently reported that a series of (E)-8-styrylcaffeines and (E)-2-styrylbenzimidazoles are moderate to very potent competitive inhibitors of monoamine oxidase B (MAO-B). The most potent member of the series was found to be (E)-8-(3-chlorostyryl)c

Synthesis and A1-adenosine receptors affinities of purino[7,8- c]quinazoline-8,10(9H,11H)-diones as rigid analogues of 8-arylxanthines

Title compounds were prepared by a cyclocondensation reaction between 8- (2-aminophenyl)xanthines and trialkyl orthoesters. Some of them showed activities as A1-adenosine receptor antagonists with binding values in the micromolar range. Results