Results 1 to 10 of about 26,240 (223)

Proton-Conducting Polymeric Membranes Based on 1,2,4-Triazole [PDF]

open access: yesMembranes, 2023
In this review, a comparative analysis of the literature and our own results obtained in the study of the physicochemical, dielectric, and proton-conducting properties of composite polymer materials based on 1H-1,2,4-triazole has been carried out. It has
Galina F. Prozorova   +1 more
doaj   +4 more sources

1-Phenyl-2-(1H-1,2,4-triazol-1-yl)ethanone [PDF]

open access: yesActa Crystallographica Section E, 2008
In the molecule of the title compound, C10H9N3O, the triazole and phenyl rings are nearly perpendicular to each other, with a dihedral angle of 88.72 (4)°. In the crystal structure, intermolecular C—H...O and C—H...N hydrogen bonds
Özden Özel Güven   +3 more
doaj   +4 more sources

Synthesis of Substituted 1,2,4-Triazole-3-Thione Nucleosides Using E. coli Purine Nucleoside Phosphorylase [PDF]

open access: yesBiomolecules
1,2,4-Triazole derivatives have a wide range of biological activities. The most well-known drug that contains 1,2,4-triazole as part of its structure is the nucleoside analogue ribavirin, an antiviral drug. Finding new nucleosides based on 1,2,4-triazole
Ilya V. Fateev   +22 more
doaj   +2 more sources

3-Phenyl-1H-1,2,4-triazol-5-amine–5-phenyl-1H-1,2,4-triazol-3-amine (1/1) [PDF]

open access: yesActa Crystallographica Section E, 2009
In the title compound, C8H8N4·C8H8N4, two tautomers, viz. 3-phenyl-1,2,4-triazol-5-amine and 5-phenyl-1,2,4-triazol-3-amine, are crystallized together in equal amounts.
Anton V. Dolzhenko   +4 more
doaj   +5 more sources

The search for new 4-amino-5-methyl-4H-1,2,4-triasole-3-thion derivatives with diuretic activity [PDF]

open access: yesZaporožskij Medicinskij Žurnal, 2018
1,2,4-Triazole derivatives have been widely used in medical practice due to their wide spectrum of biological activities and low toxicity, as they have 1,2,4-triazole cycle in their structure.
T. V. Kravchenko
doaj   +3 more sources

Search for New Compounds with Anti-Inflammatory Activity Among 1,2,4-Triazole Derivatives [PDF]

open access: yesMolecules
Compounds containing the 1,2,4-triazole moiety in their structure exhibit broad biological activities. Many of these compounds demonstrate anti-inflammatory activity in vitro through various mechanisms, such as inhibiting COX-1/COX-2 and LOX, modulating ...
Teresa Glomb   +4 more
doaj   +2 more sources

Millimeter/submillimeter Spectrum And Precise Equilibrium Structure Of 1h-1,2,4-triazole [PDF]

open access: yes, 2022
1H-1,2,4-Triazole is a five membered aromatic heterocycle with 3 inequivalent nitrogen atoms. This molecule exists as an equilibrium of two tautomers; 1H-1,2,4-Triazole (\textit{C$_{s}$}) and 4H-1,2,4-triazole (\textit{C$_{2v}$}), with the 1H tautomer ...
Bunn, Hayley
core   +1 more source

Modern approaches to studying the antimicrobial and antifungal activities of new 1,2,4-triazole derivatives

open access: yesФармацевтичний журнал, 2022
1,2,4-Triazole and its derivatives are a promising class of organic compounds. For a long time, they remain in the spotlight due to a number of unique properties: high ability to chemical transformations, the presence of various types of biological ...
M. V. Ogloblina   +2 more
doaj   +1 more source

Review of the research on the influence of different functional substituents of new 1,2,4-triazole derivatives on the compounds biological properties

open access: yesФармацевтичний журнал, 2022
Today, 1,2,4-triazole derivatives are a promising class of organic compounds. This is caused, first of all, by the possibility of various chemical modifications of the 1,2,4-triazole fragment due to the addition of typical pharmacophores, which ...
M. V. Ogloblina   +2 more
doaj   +1 more source

The synthesis of 4-amino-5-(quinolin-2-yl)-4H-1,2,4-triazole-3-thiol and its interaction with aldehydes

open access: yesЖурнал органічної та фармацевтичної хімії, 2021
Aim. To synthesize 4-amino-5-(quinolin-2-yl)-4H-1,2,4-triazole-3-thiol and study its reactivity in the reaction with aldehydes. Results and discussion.
D. М. Zozulynets   +2 more
doaj   +1 more source

Home - About - Disclaimer - Privacy