The reaction between thiols and 8-azidoadenosine derivatives
- 1 September 1976
- journal article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 3 (9) , 2331-2340
- https://doi.org/10.1093/nar/3.9.2331
Abstract
Thiols react at room temperature in dilute solution with 8-azidoadenosine and its nucleotides to give the corresponding 8-aminoadenosine derivatives. The reaction which takes place in the dark is base-catalysed and is particularly rapid when dithiols, e.g. dithiothreitol are used.Keywords
This publication has 8 references indexed in Scilit:
- 8‐Azido‐ADP, a covalent‐binding inhibitor of mitochondrial adenine nucleotide translocationFEBS Letters, 1976
- Interaction of the photoaffinity label 8‐azido‐ADP with glutamate dehydrogenaseFEBS Letters, 1976
- Photoaffinity labeling of adenosine cyclic 3',5'-monophosphate binding sites of human red cell membranesBiochemistry, 1975
- Photoaffinity labeling of a protein kinase from bovine brain with 8-azidoadenosine 3',5'-monophosphateBiochemistry, 1975
- Interactions of a Photo-Affinity ATP Analog with Cation-Stimulated Adenosine Triphosphatases of Human Red Cell MembranesProceedings of the National Academy of Sciences, 1974
- Studies of Nucleosides and Nucleotides. XXXVIII. Synthesis of 8-Bromoadenosine NucleotidesCHEMICAL & PHARMACEUTICAL BULLETIN, 1969
- Purine Nucleosides. IX. The Synthesis of 9-β-D-Ribofuranosyl Uric Acid and Other Related 8-Substituted Purine Ribonucleosides1Journal of the American Chemical Society, 1965
- Synthesis of nucleotide anhydrides by anion exchangeBiochimica et Biophysica Acta (BBA) - Specialized Section on Nucleic Acids and Related Subjects, 1964