When l,N6-etheno-adenosine, 1, was treated with sodium hydroxide, it lost fluorescence and gave 3-g-D-ribofuranosyl-4-amino-5-(imidazol-2-y1) imidazole 6. Nitrosation of 6' yielded 2-asa-l,N6-etheno-adenoaine, 11 (Scheme I). Toxicity studies showed that 11 is selectively active in rat maPmnary tumo
Fluorescent derivatives of polyribonucleotides containing ε-adenosine
✍ Scribed by R.F. Steiner; W. Kinnier; A. Lunasin; J. Delac
- Book ID
- 115745391
- Publisher
- Elsevier Science
- Year
- 1973
- Weight
- 651 KB
- Volume
- 294
- Category
- Article
- ISSN
- 0005-2787
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