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

Citation
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
Citations number
43
Categorie Soggetti
Biology
Journal title
ISSN journal
07328311
Volume
13
Issue
1-3
Year of publication
1994
Pages
389 - 403
Database
ISI
SICI code
0732-8311(1994)13:1-3<389:NR.COA>2.0.ZU;2-F
Abstract
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.