Recent Advances in the Biological Activity of s-Triazine Core Compounds [PDF]
Pharmaceuticals, 2022 An effective strategy for successful chemotherapy relies on creating compounds with high selectivity against cancer cells compared to normal cells and relatively low cytotoxicity. One such approach is the discovery of critical points in cancer cells, i.e.
Danuta Drozdowska, Dawid Maliszewski
exaly +4 more sources
Antitumor Activity of s-Triazine Derivatives: A Systematic Review [PDF]
Molecules, 2023 1,3,5-triazine derivatives, also called s-triazines, are a series of containing-nitrogen heterocyclic compounds that play an important role in anticancer drug design and development.
Qiuzi Dai +8 more
doaj +4 more sources
s-Triazine Derivatives Functionalized with Alkylating 2-Chloroethylamine Fragments as Promising Antimicrobial Agents: Inhibition of Bacterial DNA Gyrases, Molecular Docking Studies, and Antibacterial and Antifungal Activity [PDF]
Pharmaceuticals, 2023 The spectrum of biological properties of s-triazine derivatives is broad and includes anti-microbial, anti-cancer, and anti-neurodegenerative activities, among others.
Dawid Maliszewski +5 more
doaj +2 more sources
Investigation of the Persistence, Toxicological Effects, and Ecological Issues of S-Triazine Herbicides and Their Biodegradation Using Emerging Technologies: A Review [PDF]
Microorganisms, 2023 S-triazines are a group of herbicides that are extensively applied to control broadleaf weeds and grasses in agricultural production. They are mainly taken up through plant roots and are transformed by xylem tissues throughout the plant system.
Sajjad Ahmad +2 more
doaj +2 more sources
Protocol for synthesis of di- and tri-substituted s-triazine derivatives [PDF]
MethodsX, 2020 The present protocol describes the synthesis of di and tri-substituted s-triazine derivatives • s-Triazine undergoes sequential nucleophilic substitution reaction but order of nucleophile is very crucial.
Ayman El-Faham +7 more
doaj +2 more sources
Asymmetrically Substituted s‐Triazine Phosphonates by One‐Step Synthesis [PDF]
ChemistryOpen, 2023 Asymmetrically substituted s‐triazine phosphonates with up to three different phosphonate groups C3N3RR'R” with R, R’, R”=PO(OR”’) and R”’=for example, methyl, ethyl, isopropyl or n‐butyl are interesting as polymer additives like flame retardants ...
Claudia Vogt +5 more
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Exploring the Potential of s-Triazine Derivatives as Novel Antifungal Agents: A Review [PDF]
PharmaceuticalsThe growing incidence and prevalence of invasive fungal infections (IFIs) and the emergence of antimicrobial resistance compound clinical antifungal therapies.
Haoyan Liao +5 more
doaj +2 more sources
s-Triazine: A Privileged Structure for Drug Discovery and Bioconjugation [PDF]
Molecules, 2021 This review provides an overview of the broad applicability of s-triazine. Our many years working with this intriguing moiety allow us to discuss its wide activity spectrum (inhibition against MAO-A and -B, anticancer/antiproliferative and antimicrobial ...
Anamika Sharma +4 more
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Computational Study on Substituted s-Triazine Derivatives as Energetic Materials [PDF]
E-Journal of Chemistry, 2012 s-Triazine is the essential candidate of many energetic compounds due to its high nitrogen content, enthalpy of formation and thermal stability. The present study explores s-triazine derivatives in which different -NO2, -NH2 and -N3 substituted azoles ...
Vikas D. Ghule +3 more
doaj +3 more sources
Biodegradation of S-Triazine Herbicides Under Saline Conditions by Paenarthrobacter ureafaciens PC, a New Halotolerant Bacterial Isolate: Insights into Both the Degradative Pathway and Mechanisms of Tolerance to High Salt Concentrations [PDF]
MicroorganismsIn this study, a halotolerant bacterial strain was isolated and identified. This bacterium was confirmed to efficiently degrade s-triazine herbicides under saline conditions.
Chunqing Fu +5 more
doaj +2 more sources