1, 2, 3-triazole and chiral Schiff base hybrids as potential anticancer agents: DFT, molecular docking and ADME studies

Y Belay, A Muller, FS Mokoena, AS Adeyinka… - Scientific Reports, 2024 - nature.com
Abstract A series of novel 1, 2, 3-triazole and chiral Schiff base hybrids 2–6 were
synthesized by Schiff base condensation reaction from pre-prepared parent component of …

[HTML][HTML] New Schiff bases derived from dimethylpyridine-1, 2, 4-triazole hybrid as cytotoxic agents targeting gastrointestinal cancers: Design, synthesis, biological …

M Strzelecka, B Wiatrak, P Jawień, Ż Czyżnikowska… - Bioorganic …, 2023 - Elsevier
In this research, a series of novel hybrid structures of dimethylpyridine-1, 2, 4-triazole Schiff
bases were designed, synthesized, and evaluated for their in vitro cytotoxic potency on …

Antiproliferative properties and structural analysis of newly synthesized Schiff bases bearing pyrazole derivatives and molecular docking studies

N Şener, S Özkinali, YC Altunoglu, S Yerlikaya… - Journal of Molecular …, 2021 - Elsevier
New pyrazole Schiff bases containing azo groups were synthesized using the condensation
reaction between p-nitrobenzaldehyde and (E)-4-(phenyl)-1-H-pyrazole-3, 5-diamine in the …

Design, synthesis, DNA binding, modeling, anticancer studies and DFT calculations of Schiff bases tethering benzothiazole-1, 2, 3-triazole conjugates

MA Almehmadi, A Aljuhani, SY Alraqa, I Ali… - Journal of Molecular …, 2021 - Elsevier
In an attempt to design and prepare a new library of anticancer candidates, focused
thiopropargylated benzothiazole was reacted with ethyl azidoacetate and/or ethyl …

Molecular hybrid of 1, 2, 3-triazole and schiff base as potential antibacterial agents: DFT, molecular docking and ADME studies

Y Belay, A Muller, P Leballo, OA Kolawole… - Journal of Molecular …, 2023 - Elsevier
Hybrid drugs help combat antibacterial drug resistance, which is an increasing problem
globally. In addition to saving time and money, hybrid drugs offer multiple benefits. Using the …

Synthesis and evaluation of antitumor activities of novel chiral 1, 2, 4-triazole Schiff bases bearing γ-butenolide moiety

X Li, XQ Li, HM Liu, XZ Zhou, ZH Shao - Organic and medicinal chemistry …, 2012 - Springer
Abstract Background 1, 2, 4-Triazole derivatives have received much attention due to their
versatile biological properties including antibacterial, antifungal, anticonvulsant …

[PDF][PDF] Synthesis, characterization and biological evaluation of heterocyclic triazole derived Schiff base ligands comprising Mn (II) complexes: Implications of their DNA …

TV Sangeetha, S Mohanapriya - Indian Journal of Chemistry …, 2021 - op.niscpr.res.in
Schiff base ligands comprising heterocyclic moieties deserve distinct consideration because
of their excellent chemotherapeutic and antioxidant properties as biologically active agents …

Design, synthesis and antiproliferative evaluation of novel 1, 2, 4-triazole/schiff base hybrids with EGFR and B-RAF inhibitory activities

HAM El-Sherief, BGM Youssif… - Anti-Cancer Agents …, 2019 - ingentaconnect.com
Background: 1, 2, 4-triazoles possess a broad spectrum of biological activities such as
analgesic, antimicrobial, antitubercular, anti-inflammatory and antineoplastic activities. This …

Antiproliferative-antimicrobial properties and structural analysis of newly synthesized Schiff bases derived from some 1, 3, 4-thiadiazole compounds

M Gür, S Yerlikaya, N Şener, S Özkınalı… - Journal of Molecular …, 2020 - Elsevier
Abstract The 1, 3, 4-thiadiazole core has been mainly used as a pharmacological scaffold in
medicinal chemistry. A series of Schiff bases derived from 5-substituted-1, 3, 4-thiadiazole-2 …

New 1, 2, 3-triazole-containing hybrids as antitumor candidates: Design, click reaction synthesis, DFT calculations, and molecular docking study

IH El Azab, HS El-Sheshtawy, RB Bakr, NAA Elkanzi - Molecules, 2021 - mdpi.com
In an effort to improve and achieve biologically active anticancer agents, a novel series of 1,
2, 3-triazole-containing hybrids were designed and efficiently synthesized via the Cu …