Nucleic acid related compounds. 82. Conversions of adenosine to inosine 5'-thioether derivatives with Aspergillus oryzae adenosine deaminase or alkyl nitrites. Substrate and inhibitory activities of inosine 5'-thioether derivatives with purine nucleoside

Article abstract of DOI:10.1080/15257779408013249

Adenosine derivatives lacking a 5'-hydroxyl group seldom act as alternative substrates of adenosine deaminases from calf intestine and other mammalian sources. A deaminase from Aspergillus oryzae deaminated adenosine 5'-thioether derivatives cleanly and m

Full text of DOI:10.1080/15257779408013249

This article was downloaded by: [University of Illinois at Urbana-Champaign]
On: 05 October 2014, At: 09:02
Publisher: Taylor & Francis
Informa Ltd Registered in England and Wales Registered Number: 1072954 Registered
office: Mortimer House, 37-41 Mortimer Street, London W1T 3JH, UK
Nucleosides and Nucleotides
Publication details, including instructions for authors and
subscription information:
http://www.tandfonline.com/loi/lncn19
Nucleic Acid Related Compounds. 82.
Conversions of Adenosine to Inosine 5′-
Thioether Derivatives with Aspergillus
oryzae Adenosine Deaminase or Alkyl
Nitrites. Substrate and Inhibitory
Activities of Inosine 5′-Thioether
Derivatives with Purine Nucleoside
Phosphorylase
Stanislaw F. Wnuk a , Johanna D. Stoeckler b & Morris J. Robins a
a Department of Chemistry , Brigham Young University , Provo, UT,
84602, U.S.A.
b Section of Molecular & Biochemical Pharmacology, Division of
Biology & Medicine , Brown University , Providence, RI, 55555,
U.S.A.
Published online: 23 Sep 2006.
To cite this article: Stanislaw F. Wnuk , Johanna D. Stoeckler & Morris J. Robins (1994) Nucleic Acid
Related Compounds. 82. Conversions of Adenosine to Inosine 5′-Thioether Derivatives with Aspergillus
oryzae Adenosine Deaminase or Alkyl Nitrites. Substrate and Inhibitory Activities of Inosine 5′-
Thioether Derivatives with Purine Nucleoside Phosphorylase, Nucleosides and Nucleotides, 13:1-3,
389-403, DOI: 10.1080/15257779408013249
To link to this article: http://dx.doi.org/10.1080/15257779408013249
PLEASE SCROLL DOWN FOR ARTICLE
Taylor & Francis makes every effort to ensure the accuracy of all the information (the
“Content”) contained in the publications on our platform. However, Taylor & Francis,
our agents, and our licensors make no representations or warranties whatsoever as to
the accuracy, completeness, or suitability for any purpose of the Content. Any opinions
and views expressed in this publication are the opinions and views of the authors,
and are not the views of or endorsed by Taylor & Francis. The accuracy of the Content
should not be relied upon and should be independently verified with primary sources
of information. Taylor and Francis shall not be liable for any losses, actions, claims,
proceedings, demands, costs, expenses, damages, and other liabilities whatsoever or

howsoever caused arising directly or indirectly in connection with, in relation to or arising
out of the use of the Content.
This article may be used for research, teaching, and private study purposes. Any
substantial or systematic reproduction, redistribution, reselling, loan, sub-licensing,
systematic supply, or distribution in any form to anyone is expressly forbidden. Terms &
Conditions of access and use can be found at http://www.tandfonline.com/page/terms-
and-conditions