75421-10-2

Upstream product

• 72331-40-9 1,3,4,7-tetrahydro-2H-1,3-diazepin-2-one 
• 77249-74-2 1,3-di(trimethylsilyl)-1,3,4,7-tetrahydro-2H-1,3-diazepin-2-one 
• 22860-91-9 2,3,5-tri-O-benzoyl-D-ribofuranosyl bromide 

Downstream Products

• 75421-14-6 C₃₁H₂₈N₂O₉ 
• 75421-15-7 C₃₁H₂₈N₂O₉ 
• 75421-16-8 C₃₁H₂₈N₂O₉ 
• 75421-17-9 C₃₁H₂₈N₂O₉ 
• 75421-11-3 1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-3,4-dihydro-1H-1,3-diazepin-2(7H)-one 
• 75421-12-4 C₃₇H₃₄N₂O₉Se 
• 75421-13-5 C₃₇H₃₄N₂O₉Se 

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