NUCLEIC-ACID RELATED-COMPOUNDS .82. CONVERSIONS OF ADENOSINE TO INOSINE 5-BETA-THIOETHER DERIVATIVES WITH ASPERGILLUS-ORYZAE ADENOSINE-DEAMINASE OR ALKYL NITRATES - SUBSTRATE AND INHIBITORY ACTIVITIES OF INOSINE 5'-THIOETHER DERIVATIVES WITH PURINE NUCLEOSIDE PHOSPHORYLASE
Sf. Wnuk et al., NUCLEIC-ACID RELATED-COMPOUNDS .82. CONVERSIONS OF ADENOSINE TO INOSINE 5-BETA-THIOETHER DERIVATIVES WITH ASPERGILLUS-ORYZAE ADENOSINE-DEAMINASE OR ALKYL NITRATES - SUBSTRATE AND INHIBITORY ACTIVITIES OF INOSINE 5'-THIOETHER DERIVATIVES WITH PURINE NUCLEOSIDE PHOSPHORYLASE, Nucleosides & nucleotides, 13(1-3), 1994, pp. 389-403
Adenosine derivatives lacking a 5'-hydroxyl group seldom act as altern
ative substrates of adenosine deaminases from calf intestine and other
mammalian sources. A deaminase from Aspergillus oryzae deaminated ade
nosine 5'-thioether derivatives cleanly and more efficiently than alky
l nitrites. The inosine derivatives were very poor alternative substra
tes and weak inhibitors of purine nucleoside phosphorylase.