N4-deriva tives of 6-azacytidine: synthesis and biological activity

Authors

  • I. V. Alexeeva Institute of Molecular Biology and Genetics, NAS of Ukraine 150, Akademika Zabolotnoho Str., Kyiv, Ukraine, 03680 Author
  • L. I. Palchikovskaya Institute of Molecular Biology and Genetics, NAS of Ukraine 150, Akademika Zabolotnoho Str., Kyiv, Ukraine, 03680 Author
  • A. S. Shalamay Institute of Molecular Biology and Genetics, NAS of Ukraine 150, Akademika Zabolotnoho Str., Kyiv, Ukraine, 03680 Author
  • S. S. Tarnavsky Institute of Molecular Biology and Genetics, NAS of Ukraine 150, Akademika Zabolotnoho Str., Kyiv, Ukraine, 03680 Author
  • L. M. Nosach D. K. Zabolotny Institute of Microbiology and Virology, NAS of Ukraine 154, Academika Zabolotnogo Str., Kyiv, Ukraine, 03680 Author
  • V. I. Zhiovnovataya D. K. Zabolotny Institute of Microbiology and Virology, NAS of Ukraine 154, Academika Zabolotnogo Str., Kyiv, Ukraine, 03680 Author
  • N. S. Dyachenko D. K. Zabolotny Institute of Microbiology and Virology, NAS of Ukraine 154, Academika Zabolotnogo Str., Kyiv, Ukraine, 03680 Author

DOI:

https://doi.org/10.7124/bc.00048C

Abstract

Different methods of the synthesis of N4-derivatives of 6-azacytidine in conditions of simplified "sililic condensation" methods were investigated. Their antivirus activity with respect to the serotype 2 adenovirus in the culture of Hep-2 cells was studied. Primary specific activity of the compounds obtained was defined. Correlation between chemical structure of the new 6-azacytidine derivatives and its biological properties is discussed.

References

Nosach LN, Diachenko NS, Butenko SI et al. Effect of 6-azacytidine for expression adenoviral genome. New approaches to chemotherapy of viral infections. Riga: Zinatne, 1991: 87-93.

Nosach LN, Dyachenko NS, Shalamay AS, Alekseeva IV, Kushko LYa, Ozvinchuk II, Zhovnovataya VL, Butenko SL, Petrovskaya IA, Drannik GN. Antiadenovirus and immunostimulating actions of 6-azacylidine. Biopolym Cell. 1996; 12(1):75-85.

Petrusha NA. [Toxico-pharmacological properties of 6-azacytidine]. Farmakol Toksikol. 1987;50(2):75-6.

Levenko BA, Semenyuk DV, Kunakh VA et al. The study of the effect of derivatives of 6-azacytidine on the growth of isolated plant tissues. Exper. plant genetics. Kiev: Naukova Dumka, 1982. 116 p.

Chernetskiy VP. Synthesis antimetabolites nucleic acid metabolism and their use in chemotherapy molecular diseases. Vistnyk AN URSR. 1971;(8): 30-41.

Alekseeva IV, Pal’chikovskaya LI, Shalamai AS, Ognyanik SS, Morgart NV, Petrusha NA. Synthesis of N1-substituted 6-azacytosines and their biological activity. Pharmaceutical Chemistry Journal. 1994;28(4):227–30.

Cristescu C, Sitaru S. As-triazine derivatives with potential therapeutic action. XI. Thionation of 6-methylthio-as-triazine-3,5 (2H, 4H)-dione. Revue Roumaine Chimie. 1971; 16(1):135-41.

Gordon A, Ford P. Sputnik Khimika. M.: Mir, 1976; 541 p.

Ognyanik SS, Tarnavsky SS, Sikora LI, Alekseeva IV. Synthesis and spectroscopic study of 3-thio-6-alkylaminosubstituted 1,2,4-triazines-5. Ukr Khim Zh. 1988;54(11):1197-9.

?emli?ka J, ?orm F. Nucleic acids components and their analogues. LXI. The reaction of dimethylchloromethyleneammonium chloride with the 2',3',5'-tri-O-acyl derivatives of uridine and 6-azauridine; A new synthesis of 6-azacytidine. Coll Chech Chem Commun. 1965; 30(10):2052-67.

Nosach LN, Diachenko NS. Cytopathology of adenovirus infection. Kiev: Naukova Dumka, 1982. 124 p.

Galegov VA, Pushkarskaya NA, Leont'eva NA et al. The program is a pilot study of antiviral chemotherapy (anti-influenza) products and the criteria for their evaluation phase. Vopr Virusol. 1976;9(4):503-7.

Published

1997-07-20

Issue

Section

Structure and Function of Biopolymers