2021
DOI: 10.1016/j.ejmech.2021.113537
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Pyrazolotriazines: Biological activities, synthetic strategies and recent developments

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Cited by 25 publications
(4 citation statements)
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“…Furthermore, many drugs contain N-heterocycles, and some have shown biological activity. When N-heterocyclic compounds form complexes with metals, they also exhibit a variety of biological activities; nitrogen heterocyclic complexes have shown their ability to bind with DNA/BSA and exhibited anticancer activity. Among them, the metal complexes formed by pyridine derivatives demonstrate good antitumor activity and multiple forms of antitumor applications. A small amount of metal complexes produced by pyrazine derivatives also display anticancer activity. …”
Section: Introductionmentioning
confidence: 99%
“…Furthermore, many drugs contain N-heterocycles, and some have shown biological activity. When N-heterocyclic compounds form complexes with metals, they also exhibit a variety of biological activities; nitrogen heterocyclic complexes have shown their ability to bind with DNA/BSA and exhibited anticancer activity. Among them, the metal complexes formed by pyridine derivatives demonstrate good antitumor activity and multiple forms of antitumor applications. A small amount of metal complexes produced by pyrazine derivatives also display anticancer activity. …”
Section: Introductionmentioning
confidence: 99%
“…1,2,4-Triazine-based compounds and their fused congeners have anticancer, antimicrobial, antifungal, anti-inflammatory, antimalarial, and antiviral properties [ 1 , 2 , 3 , 4 ]. Since 1,2,4-triazines fused with five-membered heterocycles are considered bio-isosteres with a purine core, these derivatives are the focus of drug design [ 5 , 6 , 7 , 8 , 9 , 10 , 11 ]. However, 1,2,4-triazines possessing specific photophysical properties have seldom been used in optoelectrical research.…”
Section: Introductionmentioning
confidence: 99%
“…They proved to be agrochemical growth regulators in Cucumis sativus cultures [11]. In turn, compounds containing a triazine fragment [12][13][14][15] and their fused derivatives, viz. imidazo [4,5-e] [1,2,4]triazines (6-azapurines), are characterized by a wide profile of biological activity [16,17].…”
Section: Introductionmentioning
confidence: 99%