Immobilisation of tubercidin and nebularine via 2′,3′-cyclic acetals: Biospecific and non-specific interaction of affinity resins with adenosine deaminase
- 1 September 1979
- journal article
- research article
- Published by Elsevier in Carbohydrate Research
- Vol. 74 (1) , 117-125
- https://doi.org/10.1016/s0008-6215(00)84769-2
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Substrate- and product-affinity resins for adenosine deaminase obtained by immobilisation of adenosine and inosine via 2',3'-cyclic acetal derivativesCarbohydrate Research, 1978
- Agarose linked adenosine and guanosine-5′-monophosphate; a new general method for the coupling of ribonucleotides to polymers through their cis-diolsNucleic Acids Research, 1975
- The mode of adsorption of proteins to aliphatic and aromatic amines coupled to cyanogen bromide-activated agaroseBiochimica et Biophysica Acta (BBA) - General Subjects, 1974
- [9] Hydrophobic chromatographyPublished by Elsevier ,1974
- Hydrophobic Chromatography: Use for Purification of Glycogen SynthetaseProceedings of the National Academy of Sciences, 1973
- Potential transition state analog for adenosine deaminaseJournal of the American Chemical Society, 1970
- Pyrrolopyrimidine nucleosides. III. Total synthesis of toyocamycin, sangivamycin, tubercidin, and related derivativesJournal of the American Chemical Society, 1969
- The gel-filtration behaviour of proteins related to their molecular weights over a wide rangeBiochemical Journal, 1965
- A purification of adenosine deaminase from the superficial mucosa of calf intestineBiochimica et Biophysica Acta, 1962
- Thiation of Nucleosides. I. Synthesis of 2-Amino-6-mercapto-9-β-D-ribofuranosylpurine (“Thioguanosine”) and Related Purine Nucleosides1Journal of the American Chemical Society, 1958