(±)-7-deazaaristeromycin lacking the hydroxymethyl substituent

(±)-7-deazaaristeromycin lacking the hydroxymethyl substituent 3-Deaza- and 7-Deaza-5'-noraristeromycin and Their Antiviral Properties Synthesis and antiviral evaluation of 6'-substituted aristeromycins: potential mechanism-based inhibitors of S-adenosylhomocysteine hydrolase The synthesis and antiviral properties of (.+-.)-5'-noraristeromycin and related purine carbocyclic nucleosides. A new lead for anti-human cytomegalovirus agent design 4'-Modified analogs of aristeromycin and neplanocin A: synthesis and inhibitory activity toward S-adenosyl-L-homocysteine hydrolase Carbocyclic analog of 3-deazaadenosine: a novel antiviral agent using S-adenosylhomocysteine hydrolase as a pharmacological target Nucleosides and nucleotides. 142. an alternative synthesis of and its antiviral activity Potential inhibitors of S-adenosylmethionine-dependent methyltransferases. 9. 2',3'-Dialdehyde derivatives of carbocyclic purine nucleosides as inhibitors of S-adenosylhomocysteine hydrolase Synthesis and antiviral activity of some new S-adenosyl-L-homocysteine derivatives Inactivation of S-Adenosyl-<scp>l</scp>-homocysteine Hydrolase by 6‘-Cyano-5‘,6‘-didehydro- 6‘-deoxyhomoadenosine and 6‘-Chloro-6‘- cyano-5‘,6‘-didehydro-6‘-deoxyhomoadenosine. Antiviral and Cytotoxic Effects