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Collect. Czech. Chem. Commun. 1962, 27, 87-93
https://doi.org/10.1135/cccc19620087

Nucleic acids components and their analogues. XIV. 6-Azacytidine and some of its N(4)-derivatives

V. Černěckij, S. Chládek, F. Šorm and J. Smrt

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  • Amblard Franck, LeCher Julia C., De Ramyani, Goh Shu Ling, Li Chengwei, Kasthuri Mahesh, Biteau Nicolas, Zhou Longhu, Tber Zahira, Downs-Bowen Jessica, Zandi Keivan, Schinazi Raymond F.: Synthesis of Novel N4-Hydrocytidine Analogs as Potential Anti-SARS-CoV-2 Agents. Pharmaceuticals 2022, 15, 1144. <https://doi.org/10.3390/ph15091144>
  • Kaneko Masakatsu, Kimura Misako, Murofushi Yoshinobu, Yasumoto Takashi, Iijima Yasuteru, Yamazaki Mitsuo: Studies on Griseolic Acid Derivatives X. Synthesis and Phosphodiesterase Inhibitory Activity of 2-Substituted Derivatives of Griseolic Acid. Nucleosides and Nucleotides 1992, 11, 865. <https://doi.org/10.1080/07328319208021746>
  • Prior J J, Santi D V: On the mechanism of the acid-catalyzed hydrolysis of uridine to uracil. Evidence for 6-hydroxy-5,6-dihydrouridine intermediates. Journal of Biological Chemistry 1984, 259, 2429. <https://doi.org/10.1016/S0021-9258(17)43370-9>
  • Jiřička Z., Smetana K., Janků I., Elis J., Novotný J.: Studies on 6-azauridine and 6-azacytidine—I. Biochemical Pharmacology 1965, 14, 1517. <https://doi.org/10.1016/0006-2952(65)90005-5>
  • Škoda J., Šorm F.: Biosynthesis of co-polymers of uridylic and cytidylic acids with 6-azacytidylic acid. Biochimica et Biophysica Acta (BBA) - Specialized Section on Nucleic Acids and Related Subjects 1964, 91, 352. <https://doi.org/10.1016/0926-6550(64)90267-1>
  • Wagner G., Pischel H.: Glucoside von Mercaptopyridinen und deren Oxydationsprodukte. 3. Mitt. über „Glykoside von Heterocyclen”︁. Archiv der Pharmazie 1963, 296, 576. <https://doi.org/10.1002/ardp.19632960904>
  • Žemlička J., Smrt J., Šorm F.: The reaction of 2′,3′,5′-tri-o-acyl-6-azauridines with dimethylchloromethyleneammonium chloride a synthesis of 6-azacytidine. Tetrahedron Letters 1962, 3, 397. <https://doi.org/10.1016/S0040-4039(00)70889-6>