Triazoles and their derivatives: Chemistry, synthesis, and therapeutic applications

MM Matin, P Matin, MR Rahman… - Frontiers in molecular …, 2022 - frontiersin.org
Among the nitrogen-containing heterocyclic compounds, triazoles emerge with superior
pharmacological applications. Structurally, there are two types of five-membered triazoles: 1 …

Recent developments in mitogen activated protein kinase inhibitors as potential anticancer agents

VJ Singh, B Sharma, PA Chawla - Bioorganic Chemistry, 2021 - Elsevier
The mitogen activated protein kinase (MAPK) belongs to group of kinase that links the
extracellular stimuli to intracellular response. The MAPK signalling pathway (RAS-RAF-MEK …

Design, synthesis, molecular modeling, anticancer studies, and density functional theory calculations of 4-(1, 2, 4-triazol-3-ylsulfanylmethyl)-1, 2, 3-triazole derivatives

A Al Sheikh Ali, D Khan, A Naqvi, FF Al-Blewi… - ACS …, 2020 - ACS Publications
New conjugates of substituted 1, 2, 3-triazoles linked to 1, 2, 4-triazoles were synthesized
starting from the appropriate S-propargylated 1, 2, 4-triazoles 7 and 8. Ligation of 1, 2, 4 …

Unravelling the anticancer potency of 1,2,4-triazole-N-arylamide hybrids through inhibition of STAT3: synthesis and in silico mechanistic studies

A Turky, AH Bayoumi, FF Sherbiny, K El-Adl… - Molecular …, 2021 - Springer
The discovery of potent STAT3 inhibitors has gained noteworthy impetus in the last decade.
In line with this trend, considering the proven biological importance of 1, 2, 4-triazoles …

Hetero-bimetallic transition metal-substituted Krebs-type polyoxometalate with N-chelating ligand as anticancer agents

HZ Zhang, HX Zhao, WH Chang, XY Liu, P Chen… - Tungsten, 2023 - Springer
A novel hetero-bimetallic transition metal (SbV/MnII)-substituted Krebs-type polyoxometalate
(POM) with N-chelating ligand H4Na4 [Mn4 (H2O) 4 (trz) 2 (SbO2) 2 (SbW9O33) 2]· 20H2O …

New 4-(arylidene) amino-1, 2, 4-traizole-5-thiol derivatives and their acyclo thioglycosides as α-glucosidase and α-amylase inhibitors: Design, synthesis, and …

H El Sayed, MMK Farahat, LF Awad, M Balbaa… - Journal of Molecular …, 2022 - Elsevier
Abstract A series of 1, 2, 4-triazole Schiffs bases 3-9 and their respective acyclo
thioglycosides 10-15 based α-glucosidase and α-amylase inhibitors were synthesized under …

Molecular docking studies, biological evaluation and synthesis of novel 3-mercapto-1, 2, 4-triazole derivatives

J Ghanaat, MA Khalilzadeh, D Zareyee - Molecular diversity, 2021 - Springer
Synthesis of bioactive heterocyclic compounds having effective biological activity is an
essential research area for wide-ranging applications. In this study, a conventional …

[HTML][HTML] Synthesis and structural proof of novel oxazolo [5, 4-d] pyrimidine derivatives as potential VEGFR2 inhibitors. In vitro study of their anticancer activity

A Sochacka-Ćwikła, A Regiec, Ż Czyżnikowska… - Bioorganic …, 2024 - Elsevier
The present study aimed to design and synthesize novel 6-N-benzyloxazolo [5, 4-d]
pyrimidin-7 (6H)-imines 3a-j as possible inhibitors of the vascular endothelial growth factor …

Synthesis, properties and biological potential some condensed derivatives 1, 2, 4-triazole

A Gotsulya, T Brytanova - Journal of Faculty of Pharmacy of Ankara …, 2022 - dergipark.org.tr
Objective: The aim of the work was to develop effective methods for the synthesis of
biologically active heterocyclic systems containing pyrrole, indole and 1, 2, 4-triazole. In this …

Novel semisynthetic betulinic acid− triazole hybrids with in vitro antiproliferative potential

G Nistor, A Mioc, M Mioc, M Balan-Porcarasu, R Ghiulai… - Processes, 2022 - mdpi.com
Betulinic acid, BA, is a lupane derivative that has caught the interest of researchers due to
the wide variety of pharmacological properties it exhibits towards tumor cells. Because of …