Results 111 to 120 of about 45,356 (184)

Synthesis of 5-(2-aminoethoxy)-3-methyl-1-phenyl-1H-pyrazolo[4,3-E][1,2,4]triazine

, 2005
A variety of naturally occurring O- and N-derivatives of 1H-pyrazolo[4,3-e][1,2,4]triazine exhibit an interesting combination of biological activity [1,2].[...
Mariusz Mojzych
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3-Cyano-4-Hydroxy-1,4-Dihydro-[1,2,4]Triazolo[5,1-C][1,2,4]Triazine, Compound with Anti-Glycating and Anti-Glycoxidation Activities

, 2022
Изобретение относится к области органической химии, а именно к 3-циано-4-гидрокси-[1,2,4]триазоло[5,1-с][1,2,4]триазину формулы 1, который обладающей антигликирующей и антигликоксидационной активностями. Технический результат: обеспечение антигликирующей
Chupakhin, O. N., Чупахин, О. Н., Litvinov, R. A., Yakovlev, D. S., Спасов, А. А., Русинов, В. Л., Султанова, К. Т., Литвинов, Р. А., Sultanova, K. T., Дрокин, Р. А., Drokin, R. A., Spasov, A. A., Rusinov, V. L., Воинков, Е. К., Voinkov, E. K., Чарушин, В. Н., Яковлев, Д. С., Гасайниева, А. Г., Charushin, V. N., Gasajnieva, A. G.   +19 more
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Triazine-Modified 7‑Deaza-2′-deoxyadenosines: Better Suited for Bioorthogonal Labeling of DNA by PCR than 2′-Deoxyuridines

, 2019
6-Ethynyl-1,2,4-triazine is a small bioorthogonally reactive group we applied for fluorescent labeling of oligonucleotides by Diels–Alder reactions with inverse electron demand. We synthetically attached this functional group to the 7-position of 7-deaza-
Péter Kele, Ulrike Reisacher, Gergely B. Cserép (6796067), Hans-Achim Wagenknecht, Gergely B. Cserép, Ralf Strasser, Ulrike Reisacher (6796061), Hans-Achim Wagenknecht (1409563), Bastian Groitl (6796064), Ralf Strasser (1615420), Péter Kele (1409560), Bastian Groitl   +11 more
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An overview on the recent developments of 1,2,4-triazine derivatives as anticancer compounds

, 2017
The synthesis, the antitumor activity, the SAR and, whenever described, the possible mode of action of 1,2,4-triazine derivatives, their N-oxides, N,. N'-dioxides as well as the benzo- and hetero-fused systems are reported. Herein are treated derivatives
Barraja, Paola, Barbara Parrino, Carbone, Anna, Anna Carbone, Stella Cascioferro, Montalbano, Alessandra, Patrizia Diana, Diana, Patrizia, Cirrincione, Girolamo, Girolamo Cirrincione, Spanò, Virginia, Virginia Spanò, Parrino, Barbara, Paola Barraja, Cascioferro, Stella, Alessandra Montalbano   +15 more
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Synthesis and Characterization Antifungal Fluorine Substituted Fused Heterobicyclic Nitrogen Systems Containing 1,2,4-triazine Moiety

, 2018
Synthesis of some new full fluorinated heterobicyclic nitrogen systems containing 1,2,4-triazine moiety (4-10) have been deduced from heterocyclization of 6-(2'-trifluoroacetylamino)phenyl-3-(4'-fluorophenyl-1,2,4-triazin-5-one (3) with active oxo / halo-
Ola Ahmad Abu Ali
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Synthesis and antifungal activity of 4-substituted-3, 7 –dimethylpyrazolo [3,4-e] [1,2,4] triazine

, 2002
664-667A convenient synthesis and antifungal activity of four compounds namely 2-(3, 7-dimethyl-4H-pyrazolo[3,4-e][1,2,4]triazin-4-yl)acetic acid 2, 3,7-dimethyl-4-(4-methylphenyl-pyrazolo[3,4-e][1,2,4]triazine 3, 4-(3,7-dimethyl-4H-pyrazolo[3,4-e][1 ...
Tewari, Ashish Kumar, Verma, H N, Mishra, Anil, Mishra, Lily   +3 more
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1,2,4‐Triazines

ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
C. W. Lindsley, M. E. Layton
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1,2,4‐Triazine N‐Oxides

ChemInform, 2002
AbstractFor Abstract see ChemInform Abstract in Full Text.
D.N Kozhevnikov, V.L Rusinov, O.N Chupakhin   +2 more
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Antimalarials. 3. 1,2,4-Triazines

Journal of Medicinal Chemistry, 1976
The syntheses of a number of substituted 1,2,4-triazines as potential antimalarials are described. The structural requirements for antimalarial activity are discussed with reference to the substituents of a phenyl group in the 6 position and amino groups at the 3 and 5 positions.
L C, March, G S, Bajwa, J, Lee, K, Wasti, M M, Joullíe   +4 more
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3-Amino-1,2,4-triazine

Acta Crystallographica Section C Crystal Structure Communications, 2002
In the crystal structure of 3-amino-1,2,4-triazine, C(3)H(4)N(4), the molecules form hydrogen-bonded chains that are almost parallel to the b axis (3.2 degrees), and which are inclined to the a and c axes by approximately 21 and approximately 69 degrees, respectively.
Genivaldo Julio, Perpétuo, Jan, Janczak
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