One-pot multicomponent polymerization, metal-, and non-metal-catalyzed synthesis of organoselenium compounds
The one-pot multicomponent synthetic strategy of organoselenium compounds represents
an alternative and robust protocol to the conventional multistep methods. During the last …
an alternative and robust protocol to the conventional multistep methods. During the last …
Promising organoselenium corrosion inhibitors for C1018-steel in hydrochloric acid environments
Abstract Background Novel organoselenium (OSe) corrosion inhibitors, namely 2-(((4-
(benzylselanyl) phenyl) imino) methyl)-5-nitrophenol (BSeOH) and its Ni (II) chelate [Ni …
(benzylselanyl) phenyl) imino) methyl)-5-nitrophenol (BSeOH) and its Ni (II) chelate [Ni …
Novel organoselenium-based N-mealanilic acid and its zinc (II) chelate: Catalytic, anticancer, antimicrobial, antioxidant, and computational assessments
S Shaaban, MSS Adam, NM El-Metwaly - Journal of Molecular Liquids, 2022 - Elsevier
Herein we report the synthesis of two novel Zn (II)-complexes (Zn (LgSe) 2 and Zn (Lg) 2)
starting from 4-((4-(methylselanyl) phenyl) amino)-4-oxobut-2-enoic acid (HLgSe) and 4-oxo …
starting from 4-((4-(methylselanyl) phenyl) amino)-4-oxobut-2-enoic acid (HLgSe) and 4-oxo …
Novel water-soluble organoselenocyanates and symmetrical diselenides tethered N-succinanilate and N-maleanilate as corrosion inhibitors for reinforced steel in the …
The anti-corrosive accomplishment of novel water-soluble organoselenocyanates and
symmetrical diselenides tethered N-succinanilate and N-maleanilate was evaluated for …
symmetrical diselenides tethered N-succinanilate and N-maleanilate was evaluated for …
Macrocycles and supramolecules as antioxidants: Excellent scaffolds for development of potential therapeutic agents
Oxidative stress due to the high levels of reactive oxygen species (ROS) that damage
biomolecules (lipids, proteins, DNA) results in acute inflammation. However, without proper …
biomolecules (lipids, proteins, DNA) results in acute inflammation. However, without proper …
Synthesis and biochemical studies of novel organic selenides with increased selectivity for hepatocellular carcinoma and breast adenocarcinoma
Nineteen organoselenides were synthesized and tested for their intrinsic cytotoxicity in
hepatocellular carcinoma (HepG2) and breast adenocarcinoma (MCF-7) cell lines and their …
hepatocellular carcinoma (HepG2) and breast adenocarcinoma (MCF-7) cell lines and their …
Antimicrobial evaluation and docking study of some new substituted benzimidazole-2yl derivatives
Benzimidazoles incorporated biologically active heterocycles such as quinoline, triazine-3-
thione, thiazole and thiadiazole, were synthesized utilizing 2-acetylbenzimidazole as a …
thione, thiazole and thiadiazole, were synthesized utilizing 2-acetylbenzimidazole as a …
Urea-functionalized organoselenium compounds as promising anti-HepG2 and apoptosis-inducing agents
Hepatocellular carcinoma is a highly aggressive and difficult-to-treat type of cancer.
Incorporating urea functionality into the backbone of organoselenium compounds is …
Incorporating urea functionality into the backbone of organoselenium compounds is …
Novel organoselenium redox modulators with potential anticancer, antimicrobial, and antioxidant activities
Novel organic selenides were developed in good yields (up to 91%), and their chemical
entities were confirmed by IR, MS, and 1H-and 13C-NMR spectroscopy. Their anticancer …
entities were confirmed by IR, MS, and 1H-and 13C-NMR spectroscopy. Their anticancer …
Combinatorial synthesis, in silico, molecular and biochemical studies of tetrazole-derived organic selenides with increased selectivity against hepatocellular …
Novel tetrazole-based diselenides and selenoquinones were synthesized via azido-Ugi and
sequential nucleophilic substitution (SN) strategy. Molecular docking study into mammalian …
sequential nucleophilic substitution (SN) strategy. Molecular docking study into mammalian …