254440-87-4

Upstream product

• 23316-67-8 2,3,5-tri-O-benzoyl-β-D-ribofuranosyl-1-carbonitrile 
• 6974-32-9 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 
• 6066-82-6 1-hydroxy-pyrrolidine-2,5-dione 
• 23316-68-9 (2R,3R,4R,5R)-3,4-bis(benzoyloxy)-5-((benzoyloxy)methyl)tetrahydrofuran-2-carboxylic acid 

Downstream Products

• 254440-88-5 N-(2,5-Anhydro-3,4,6-tri-O-benzoyl-D-allonoyl)-N'-(3-dimethylamino-4,5-dihydro-5-oxo-1,2,4-triazin-6-yl)hydrazine 
• 254440-89-6 6-Dimethylamino-3-(2',3',5'-tri-O-benzoyl-β-D-ribofuranosyl)-1,2,4-triazolo[3,4-f][1,2,4]triazin-8(7H)-one 
• 254440-92-1 6-Dimethylamino-8-hydrazino-3-(2',3',5'-tri-O-benzoyl-β-D-ribofuranosyl)-1,2,4-triazolo[3,4-f][1,2,4]triazine 
• 254440-91-0 8-Chloro-6-dimethylamino-3-(2',3',5'-tri-O-benzoyl-β-D-ribofuranosyl)-1,2,4-triazolo[3,4-f][1,2,4]triazine 
• 254440-93-2 6-Dimethylamino-3-(2',3',5'-tri-O-benzoyl-β-D-ribofuranosyl)-1,2,4-triazolo[3,4-f][1,2,4]triazine 

Relevant academic research and scientific papers

Synthesis of C-ribosyl 1,2,4-triazolo[3,4-f][1,2,4]triazines as inhibitors of adenosine and AMP deaminases

Modified C-nucleosides and nucleotides with an enhanced tendency to undergo covalent hydration are of interest as potential inhibitors of adenosine deaminase (ADA) and AMP deaminase, respectively. In a search for such compounds we have synthesized 6-dimet

BICYCLIC HETEROCYCLES, METHOD FOR PRODUCING THEM AND THEIR USE AS HERBICIDES AND PHARMACEUTICAL AGENTS

Methods and compounds for inhibiting the enzymes adenosine monophosphate deaminase or adenoside deaminase are provided. Such methods and compounds are useful in agriculture, horticulture and/or pharmacology as, for example, active compounds for crop prote