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Targeting breast cancer with 1,2,4-trioxanes: synthesis, cytotoxicity, and molecular docking insights. [PDF]
RSC AdvYadav P +8 more
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Sonosynthesis of new functionalized optically active triazines <i>via</i> double Mannich reaction: antibacterial potential and <i>in silico</i> docking study. [PDF]
RSC AdvAli HA +3 more
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Exploring the versatility of heterocyclic compounds containing nitrogen atoms (triazoles): a comprehensive review. [PDF]
RSC AdvAkram M, Tamminana R.
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Chemistry of 1,2,4‐triazines, XV. First metalation of 1,2,4‐triazine derivatives
Liebigs Annalen Der Chemie, 1993Abstract5‐Methoxy‐1,2,4‐triazines 2 were lithiated with lithium 2,2,6,6‐tetramethylpiperidide and the formed 6‐lithio‐5‐methoxy‐1,2,4‐triazines 4 trapped with aldehydes or iodine.
Nelly Plé +4 more
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ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
C. W. Lindsley, M. E. Layton
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AbstractFor Abstract see ChemInform Abstract in Full Text.
C. W. Lindsley, M. E. Layton
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ChemInform, 2002
AbstractFor Abstract see ChemInform Abstract in Full Text.
D.N Kozhevnikov +2 more
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AbstractFor Abstract see ChemInform Abstract in Full Text.
D.N Kozhevnikov +2 more
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Antimalarials. 3. 1,2,4-Triazines
Journal of Medicinal Chemistry, 1976The 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 +4 more
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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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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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Journal of Pharmaceutical Sciences, 1980
To develop nonacidic, nonsteroidal anti-inflammatory agents without GI complications, a series of asymmetric triazines was synthesized and evaluated for anti-inflammatory efficacy in the carrageenan-induced pedal edema assay. Toxicity was estimated by determination of approximate LD50 values in mice.
W P, Heilman +5 more
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To develop nonacidic, nonsteroidal anti-inflammatory agents without GI complications, a series of asymmetric triazines was synthesized and evaluated for anti-inflammatory efficacy in the carrageenan-induced pedal edema assay. Toxicity was estimated by determination of approximate LD50 values in mice.
W P, Heilman +5 more
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ChemInform Abstract: 1,2,4‐TRIAZINES PART 10, DIMERIZATIONS OF 1,2,4‐TRIAZINES
Chemischer Informationsdienst, 1973AbstractAus den 1,2,4‐Triazinen (I) mit freier 5‐Stellung erhält man in der angegebenen Weise bei der Behandlung mit Methylat oder mit Kaliumcyanid über anionische Zwischenstufen Dimere wie (II).
D. K. KRASS, T.‐K. CHEN, W. W. PAUDLER
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