New metal complexes of sulfonamide: Synthesis, characterization, in‐vitro anticancer, anticholinesterase, antioxidant, and antibacterial studies
In this research work a sulfonamide from tranexamic acid has been synthesized followed by
its metal complexation. p‐Bromo benzene sulfonyl chloride was used to synthesize …
its metal complexation. p‐Bromo benzene sulfonyl chloride was used to synthesize …
Coumarin or benzoxazinone based novel carbonic anhydrase inhibitors: synthesis, molecular docking and anticonvulsant studies
Among many others, coumarin derivatives are known to show human carbonic anhydrase
(hCA) inhibitory activity. Since hCA inhibition is one of the underlying mechanisms that …
(hCA) inhibitory activity. Since hCA inhibition is one of the underlying mechanisms that …
Preparation, characterization, in silico and in vitro antimicrobial studies of phenothiazine-3-sulphonamide derivatives
EL Ayuk, MO Uchegbu… - …, 2024 - journal.pandawainstitute.com
The antibacterial activities of phenothiazine and sulphonamide derivatives have attracted so
much interest. In this study, the synthesis and characterization of phenothiazine-3 …
much interest. In this study, the synthesis and characterization of phenothiazine-3 …
Synthesis, biological activity and structure‐activity relationship of novel diphenylurea derivatives containing tetrahydroquinoline as carbonic anhydrase I and II …
A series of novel tetrahydroquinoline derivatives containing urea moiety was synthesized
and their in vitro inhibitory effects on the human carbonic anhydrase isoenzymes (hCA− I …
and their in vitro inhibitory effects on the human carbonic anhydrase isoenzymes (hCA− I …
Development of New Targeted Nanotherapy Combined with Magneto-Fluorescent Nanoparticles against Colorectal Cancer
GA Marcelo, D Montpeyó, J Galhano… - International Journal of …, 2023 - mdpi.com
The need for non-invasive therapies capable of conserving drug efficiency and stability
while having specific targetability against colorectal cancer (CRC), has made nanoparticles …
while having specific targetability against colorectal cancer (CRC), has made nanoparticles …
Synthesis, characterization and in vitro inhibition of metal complexes of pyrazole based sulfonamide on human erythrocyte carbonic anhydrase isozymes I and II
Sulfonamides represent an important class of biologically active compounds. A sulfonamide
possessing carbonic anhydrase (CA) inhibitory properties obtained from a pyrazole based …
possessing carbonic anhydrase (CA) inhibitory properties obtained from a pyrazole based …
[PDF][PDF] Azo-azomethine ligands with N2O2 donor atom sets and their binuclear UO2 (II) complexes: synthesis, characterization and biological activity
Two azo-azomethine ligands with N2O2 donor atom sets and their binuclear UO2 (II)-
complexes were synthesized for therapeutic uses. The ligands were derived from the …
complexes were synthesized for therapeutic uses. The ligands were derived from the …
Terbium Tetra‐Sulfosalicylate Complex as Quantitative Luminescent Sensing of Chromate Ions with High Selectivity and Sensitivity
W Yang, J **a, G Zhou, T Hu, D Ye… - Bulletin of the Korean …, 2019 - Wiley Online Library
In this study, a terbium (Ш) complex, Tb (SSA) 4 (SSA= sulfosalicylate), was synthesized and
employed to detect toxic chromate anion (CrO42−) as a visually identifiable probe …
employed to detect toxic chromate anion (CrO42−) as a visually identifiable probe …
Synthesis, characterization, antibacterial activity and VSM investigation of Fe3O4–NiCr2O4 nano oxide obtained from a new oxalato-bridged complex
The preparation of Fe 3 O 4–NiCr 2 O 4 nano-oxide (2) is reported via thermal
decomposition of [Fe (phen) 2 (H 2 O) 2] 2 [(ox) 2 Cr (μ-ox) Ni (phen)(μ-ox) Cr (ox) …
decomposition of [Fe (phen) 2 (H 2 O) 2] 2 [(ox) 2 Cr (μ-ox) Ni (phen)(μ-ox) Cr (ox) …
Reactions and effect of N-sulfonylpyrrole yielding metal complexes: Crystal structural studies
The reaction of N-toluenesulfonylpyrrole with benzonitrile at room temperature afforded 4-
methyl-N-[phenyl (1H-pyrrol-2yl) methylene] toluenesulfonamide (L). The ligand (L) was …
methyl-N-[phenyl (1H-pyrrol-2yl) methylene] toluenesulfonamide (L). The ligand (L) was …