[The benzo-1,2,3-triazine ring system as basis of potentially virustatic compounds (author's transl)].
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Adamantane↗
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Results for “Triazines”
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[Structure modification of analgesic drugs by s-triazine (author's transl)].
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Amidines↗
[Antiviral agents, XII1): 2-Amino-4-arylamino-s-triazines substituted on the nucleus (author's transl)].
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Antiviral Agents↗
[Antimycotic agents, 13. Halophenoxy-1,3,5-triazines].
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Antifungal Agents↗
[Synthesis and trichomonacidal activity of di(isopropylamino)-1,3,5-triazines].
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Animals↗
[H2-antihistaminics. 31. 1,2,5-Triazine-2,4-diamines and -2,4,6-triamines with H2-antagonistic activity].
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Amines↗
[Anticonvulsants 5. Substitution reactions in 2,4-dichlo-6-(diallyamino)-1,3,5-triazine systems].
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Animals↗
[Anthelmintic agents. 5. Long-chain and hydroheterocyclic-substituted chloro-diallylamino-1,3,5-triazines].
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Animals↗
[Central depressive substances. 7. Nuclear substituted (diallylamino)-1,3,5-triazines].
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Animals↗
[Antimycotic agents. 22. Chlor-(1-piperazinyl)-1,3,5-triazines].
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Antifungal Agents↗
Recognition of thymine by triazine fluorescent probe through intermolecular multiple hydrogen bonding.
In order to design a fluorescent probe with a long wavelength and multiple hydrogen bond sites for thymine, 3-(4-chloro-6-methylamino-1,3,5-triazinylamino)-7-dimethylamino-2-methylphenazine is synthesized by subsequently reacting neutral red and methylamine with cyanuric chloride. Its recognition behavior for thymine and its spectroscopic properties in different solvents are studied. The probe's fluorescence can be selectively quenched by thymine instead of guanine, indicating that fully complementary hydrogen bonding plays a key role in such recognition processes. In addition, the recognition mechanism of the probe for thymine and the bathochromic shift of its fluorescence spectra with the solvent polarity are also discussed.
Absorption↗
[Pyrazolo(4.3-e)as-triazine, a new heterocyclic system from Pseudomonas fluorescens Var. Pseudoiodinum].
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Cyclization↗
[Preparation and reactions of substituted (1,5-a) pyrazolo (1,3,5) triazines].
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Chemical Phenomena↗
Dimerizable redox-sensitive triazine-based cationic lipids for in vitro gene delivery.
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Animals↗
Variation in mutagenicity of s-triazine compounds tested on four Salmonella strains.
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Mutagenicity Tests↗
[Studies on triazines as future oral antidiabetics].
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Biguanides↗
Preparation of 1,2,4-triazole derivatives of s-triazines.
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Animals↗
Analogs of tetrahydrofolic acid. XXVII. Hydrophobic bonding to dihydrofolic reductase by 2-amino-4,6-disubstituted-5-alkylpyrimidines and 1-alkyl-4,6-diamino-1,2-dihydro-s-triazines.
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Chemistry, Pharmaceutical↗