77249-70-8

Upstream product

• 16205-60-0 2,3,5-tri-O-benzoyl-β-D-ribofuranosyl bromide 
• 80963-17-3 C₃₄H₃₈N₂O₈Si 
• 6974-32-9 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 
• 18023-41-1 1,3-bis-trimethylsilanyl-[1,3]diazepan-2-one 
• 80963-18-4 C₃₁H₃₀N₂O₈ 
• 22860-91-9 2,3,5-tri-O-benzoyl-D-ribofuranosyl bromide 
• 80963-16-2 2,3,5-tri-O-benzoyl-β-D-ribofuranosyl iodide 
• 19055-93-7 1,3-diazepan-2-one 

Downstream Products

• 107711-32-0 1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-4-(methylthio)tetrahydro-2H-1,3-diazepin-2-one 
• 107711-28-4 C₃₂H₂₈N₂O₈S 
• 107711-31-9 1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-4-thioxohexahydro-2H-1,3-diazepin-2-one 
• 107711-27-3 1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-4-thioxo-1,3,4,7-tetrahydro-2H-1,3-diazepin-2-one 
• 107711-26-2 1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-1,7-dihydro-2H-1,3-diazepine-2,4(3H)-dione 
• 107711-33-1 1-β-D-ribofuranosyl-4-aminotetrahydro-2H-1,3-diazepin-2-one 
• 107711-30-8 1-β-D-ribofuranosyl-4-amino-1,7-dihydro-2H-1,3-diazepine-2-one 
• 74024-66-1 1-(β-D-Ribofuranosyl)-perhydro-1,3-diazepin-2-one 
• 107711-22-8 1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)tetrahydro-2H-1,3-diazepine-2,4(3H)-dione 
• 107711-23-9 C₃₇H₃₂N₂O₉Se 

Relevant academic research and scientific papers

Cyclic Urea Nucleosides. Cytidine Deaminase Activity as a Function of Aglycon Ring Size

Five β-D-ribofuranosyl cyclic urea nucleosides (14-18), ranging in size from five to eight membered, were synthesized and evaluated as cytidine deaminase (CDA) inhibitors.The precursor protected nucleosides (9-13) were prepared by a condensation procedure

Seven-membered ring compounds as inhibitors of cytidine deaminase

Seven-membered heterocyclic nucleosides used to inhibit the deamination enzyme responsible for the inactivation of arabinosylcytosine (ara--C). Preferred nucleosides containing a seven-member aglycone are as follows: STR1 Preferred aglycones are as follow