Chitosan-based Schiff bases: Promising materials for biomedical and industrial applications
There is plenty of scope for modifying chitosan, an only polycationic natural polysaccharide,
owing to its reactive functional groups, namely hydroxyl and amino groups. Although …
owing to its reactive functional groups, namely hydroxyl and amino groups. Although …
Sericin nanoparticles: Future nanocarrier for target-specific delivery of chemotherapeutic drugs
Sericin, a by-product of silk, has been recognized as an economical glycoprotein extracted
during the silk degumming process in the textile industry. It has potent biocompatibility and …
during the silk degumming process in the textile industry. It has potent biocompatibility and …
Exploration of 1, 2, 3-triazole linked benzenesulfonamide derivatives as isoform selective inhibitors of human carbonic anhydrase
Abstract A novel series of 1, 2, 3-triazole benzenesulfonamide substituted 1, 3-
dioxoisoindolin-5-carboxylate (7a-l) inhibitors of human α-carbonic anhydrase (hCA) was …
dioxoisoindolin-5-carboxylate (7a-l) inhibitors of human α-carbonic anhydrase (hCA) was …
[HTML][HTML] Synthesis and characterization of a new developed modified-chitosan Schiff base with improved antibacterial properties for the removal of Bismarck brown R …
In this study, the synthesis of a new chitosan-based Schiff base with surface modification
using chloroethanoic acid was reported. The physicochemical attributes of the modified …
using chloroethanoic acid was reported. The physicochemical attributes of the modified …
Synthesis and characterization of citric acid-modified chitosan Schiff base with enhanced antibacterial properties for the elimination of Bismarck Brown R and …
In this study, a new chitosan Schiff base with surface modification using citric acid was
synthesized for efficient removal of pernicious dyes, namely Bismarck Brown R (BBR) and …
synthesized for efficient removal of pernicious dyes, namely Bismarck Brown R (BBR) and …
[HTML][HTML] An update on inhibitors targeting RNA-dependent RNA polymerase for COVID-19 treatment: promises and challenges
X Xu, Y Chen, X Lu, W Zhang, W Fang, L Yuan… - Biochemical …, 2022 - Elsevier
The highly transmissible variants of SARS-CoV-2, the causative pathogen of the COVID-19
pandemic, bring new waves of infection worldwide. Identification of effective therapeutic …
pandemic, bring new waves of infection worldwide. Identification of effective therapeutic …
Total synthesis of natural products using gold catalysis
Gold catalysis is an extremely enthusiastic field of investigation in the catalysis area. The
development of alternative, highly inventive, precompetitive techniques based on gold …
development of alternative, highly inventive, precompetitive techniques based on gold …
Green and efficient one-pot three-component synthesis of novel drug-like furo [2, 3-d] pyrimidines as potential active site inhibitors and putative allosteric hotspots …
H Mousavi, B Zeynizadeh, M Rimaz - Bioorganic Chemistry, 2023 - Elsevier
In this paper, an environmentally benign, convenient, and efficient one-pot three-component
reaction has been developed for the regioselective synthesis of novel 5-aroyl (or …
reaction has been developed for the regioselective synthesis of novel 5-aroyl (or …
Salicylaldehyde-diphenyl-azine skeleton-based ESIPT-coupled AIEgens with tunable emission and applicable as highly selective and sensitive Cu2+ ion sensor
Herein, we are reporting four novel salicylaldehyde-diphenyl-azine (SDPA) skeleton-based
luminogens with tunable emission synthesized using the microwave. The photophysical …
luminogens with tunable emission synthesized using the microwave. The photophysical …
Design and synthesis of 2-amino-4,6-diarylpyrimidine derivatives as potent α-glucosidase and α-amylase inhibitors: structure–activity relationship, in vitro, QSAR …
In the present study, a series of 2-amino-4, 6-diarylpyrimidine derivatives was designed,
synthesized, characterized and evaluated for their in vitro α-glucosidase and α-amylase …
synthesized, characterized and evaluated for their in vitro α-glucosidase and α-amylase …