Due to the structure of acylhydrazones both by the pharmacophore–CO–NH–N= group and by the different substituents present in the molecules of compounds of this class, various …
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 …
Objective Sulfanilamide, sulfadiazine, and dapsone were the first sulfonamides to be used to treat malaria by disrupting the folate biosynthesis process, which is essential for parasite …
B Taxak, J Devi, S Kumar, S Asija - Inorganic Chemistry Communications, 2023 - Elsevier
Inspired by the role of organotin (IV) compounds as potential pharmaceutical agents, we have synthesized a series of new diorganotin (IV) complexes (5–20) of hydrazone ligands (1 …
In the current investigation, a new class of quinazolinone N-acetohydrazides 9a-v was designed as type II multi-kinase inhibitors. The target quinazolinones were tailored so that …
YI Touahria, N Chafai, O Moumeni, A Boublia… - Journal of Molecular …, 2024 - Elsevier
This study presents a synergistic approach encompassing experimental synthesis, computational analysis, and antioxidant activity evaluation of two aromatic hydrazone …
SN Mali, A Pandey - Journal of Computational Biophysics and …, 2021 - World Scientific
Malarial parasites have been reported for moderate-high resistance towards classical antimalarial agents and henceforth development of newer novel chemical entities targeting …
In search of potent α-amylase inhibitors, herein we report the synthesis, molecular docking and QSAR study of some thiazole clubbed pyrazole hybrids (TCPH) ie, 1-((1-phenyl-3-aryl-1 …
M Duhan, J Sindhu, P Kumar, M Devi… - Journal of …, 2022 - Taylor & Francis
The present manuscript describes the synthesis, α-amylase inhibition, in silico studies and in- depth quantitative structure–activity relationship (QSAR) of a library of aroyl hydrazones …