Collect. Czech. Chem. Commun.
1966, 31, 1864-1871
https://doi.org/10.1135/cccc19661864
Nucleic acids components and their analogues. LXXXII. The fine structure of 6-azaisocytosine and its derivatives
J. Piťha, P. Fiedler and J. Gut
Crossref Cited-by Linking
- Sztanke Małgorzata, Rzymowska Jolanta, Janicka Małgorzata, Sztanke Krzysztof: Two novel classes of fused azaisocytosine-containing congeners as promising drug candidates: Design, synthesis as well as in vitro, ex vivo and in silico studies. Bioorganic Chemistry 2020, 95, 103480. <https://doi.org/10.1016/j.bioorg.2019.103480>
- Sztanke Małgorzata, Rzymowska Jolanta, Janicka Małgorzata, Sztanke Krzysztof: Synthesis, structure elucidation, determination of antiproliferative activities, lipophilicity indices and pharmacokinetic properties of novel fused azaisocytosine-like congeners. Arabian Journal of Chemistry 2019, 12, 4044. <https://doi.org/10.1016/j.arabjc.2016.04.002>
- Sztanke Małgorzata, Rzymowska Jolanta, Janicka Małgorzata, Sztanke Krzysztof: Synthesis, structure confirmation, identification of in vitro antiproliferative activities and correlation of determined lipophilicity parameters with in silico bioactivity descriptors of two novel classes of fused azaisocytosine-like congeners. Arabian Journal of Chemistry 2019, 12, 5302. <https://doi.org/10.1016/j.arabjc.2016.12.024>
- Sztanke Małgorzata, Sztanke Krzysztof, Rajtar Barbara, Świątek Łukasz, Boguszewska Anastazja, Polz-Dacewicz Małgorzata: The influence of some promising fused azaisocytosine-containing congeners on zebrafish (Danio rerio) embryos/larvae and their antihaemolytic, antitumour and antiviral activities. European Journal of Pharmaceutical Sciences 2019, 132, 34. <https://doi.org/10.1016/j.ejps.2019.02.033>
- Zálešák František, Slouka Jan, Stýskala Jakub: General Synthesis of 1-Aryl-6-azaisocytosines and Their Utilization for the Preparation of Related Condensed 1,2,4-Triazines. Molecules 2019, 24, 3558. <https://doi.org/10.3390/molecules24193558>
- Lapinski Leszek, Reva Igor, Gerega Anna, Nowak Maciej J., Fausto Rui: UV-induced transformations of matrix-isolated 6-azacytosine. The Journal of Chemical Physics 2018, 149. <https://doi.org/10.1063/1.5045735>
- Üngören Şevket Hakan, Dilekoğlu Emine, Koca İrfan: Synthesis of pyrazine-2,3-dicarbonitrile and 1,2,4-triazine-5(4H)-one derivatives from furan-2,3-diones. Chinese Chemical Letters 2013, 24, 1130. <https://doi.org/10.1016/j.cclet.2013.08.001>
- Hwang Long‐Chih, Wu Rang‐Rong, Tu Chun‐Hsien: Aromatization and ring cyclization: A better understanding on the ring cyclization mechanism of 3‐amino‐6‐hydrazino‐1,2,4‐triazin‐5(2H)‐one reacted with acetic acid in N,N‐dimethylformamide. Journal of Heterocyclic Chem 2005, 42, 851. <https://doi.org/10.1002/jhet.5570420516>
- Pal'chykovska L. H., Platonov M. O., Alexeeva I. V., Shved A. D.: Design of the potential transcription inhibitors based on the 6-azacytosine and 6-aza-iso-cytosine. Nonempirical quantum chemical analysis, synthesis and physico-chemical studies. Biopolym. Cell 2004, 20, 131. <https://doi.org/10.7124/bc.00069D>
- Hwang Long-Chih, Wang Jung-Hui, Tzeng Cherng-Chyi, Lee Gene-Hsiang, Peng Shie-Ming: Crystal Structure of 3-Amino-1,2,4-triazin-5(2H)-one. ANAL. SCI. 2002, 18, 723. <https://doi.org/10.2116/analsci.18.723>
- Mizutani Masato, Sanemitsu Yuzuru, Tamaru Yoshinao, Yoshida Zen-Ichi: Palladium-catalyzed cyclization reactions. Tetrahedron 1986, 42, 305. <https://doi.org/10.1016/S0040-4020(01)87432-9>
- Lovelette Charles A.: 1,2,4‐Triazines. Synthesis of selected members of the s‐triazolo[3,4‐f]‐ [1,2,4] triazine and tetrazolo[1,5‐f] [1,2,4] triazine ring systems. Journal of Heterocyclic Chem 1979, 16, 555. <https://doi.org/10.1002/jhet.5570160330>
- Le Count D.J., Taylor P.J.: The infrared spectra of fused 1,2,4-triazin-5-ones. Tetrahedron 1975, 31, 433. <https://doi.org/10.1016/0040-4020(75)80056-1>
- Ikehara M., Kaneko M., Sagai M.: Studies of nucleosides and nucleotides—XLVI. Tetrahedron 1970, 26, 5757. <https://doi.org/10.1016/0040-4020(70)80013-8>
- Pullman Bernard: OPENING REMARKS: QUANTUM‐MECHANICAL CALCULATIONS OF BIOLOGICAL STRUCTURES AND MECHANISMS. Annals of the New York Academy of Sciences 1969, 158, 1. <https://doi.org/10.1111/j.1749-6632.1969.tb56211.x>
- Kittler L., Berg H.: PHOTOCHEMINE ANOMALER NUCLEINSÄUREBAUSTEINE‐I. PHOTODEGRADATION VON AZAPYRIMIDINEN UND AZAPURINEN. Photochem & Photobiology 1967, 6, 199. <https://doi.org/10.1111/j.1751-1097.1967.tb08804.x>