Synthesis of 5′-Substituted Derivatives of the Pyrrolo[2,3-d]-Pyrimidine Nucleoside Sangivamycin and Their Effect on Protein Kinase A and C Activity
Author:
Publisher
Informa UK Limited
Subject
Genetics,Biochemistry
Reference11 articles.
1. Protein kinase C in transmembrane signalling
2. Suppression of malignancy targeting cyclic AMP signal transducing proteins
3. Sangivamycin, a nucleoside analogue, is a potent inhibitor of protein kinase C.
4. Suhadolnik, R. J. 1970.Nucleoside Antibiotics, 300–314. 323–346. New York: Wiley - Interscience.
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1. Total Synthesis of the Naturally Occurring Antibiotic Toyocamycin Using New and Improved Synthetic Procedures;Nucleosides and Nucleotides;1999-02
2. An Improved Synthesis of the Versatile Heterocycle, 4-Amino-6-Bromo-5-Cyanopyrrolo[2,3-d]Pyrimidine;Synthetic Communications;1998-10
3. Synthesis of Derivatives of 3-Methylxantheve and 1-Methyl-3-Isobutylxanthine 7-β-D-Ribofuranosides;Nucleosides and Nucleotides;1998-09
4. Synthesis and in vitro antitumor activity of some amino-deoxy 7-hexofuranosylpyrrolo[2,3-d]pyrimidines;Carbohydrate Research;1998-04
5. Synthesis of 5′-Fluoro-5′-deoxy-and 5′-Amino-5′-Deoxytoyocamycin and Sangivamycin and Some Related Derivatives;Nucleosides and Nucleotides;1995-11
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