Overview on developed synthesis procedures of coumarin heterocycles
MM Zeydi, SJ Kalantarian, Z Kazeminejad - Journal of the Iranian …, 2020 - Springer
Considering highly valuable biological and pharmaceutical properties of coumarins, the
synthesis of these heterocycles has been considered for many organic and pharmaceutical …
synthesis of these heterocycles has been considered for many organic and pharmaceutical …
An overview of the privileged synthetic heterocycles as urease enzyme inhibitors: structure–activity relationship
S Sepehri, M Khedmati - Archiv der Pharmazie, 2023 - Wiley Online Library
Urease is a metalloenzyme including two Ni2+ ions, found in some plants, bacteria, fungi,
microorganisms, invertebrate animals, and animal tissues. Urease acts as a significant …
microorganisms, invertebrate animals, and animal tissues. Urease acts as a significant …
Expression, Purification, and Comparative Inhibition of Helicobacter pylori Urease by Regio-Selectively Alkylated Benzimidazole 2-Thione Derivatives
The urease enzyme has been an important target for the discovery of effective
pharmacological and agricultural products. Thirteen regio-selectively alkylated …
pharmacological and agricultural products. Thirteen regio-selectively alkylated …
Designing Potent α-Glucosidase Inhibitors: A Synthesis and QSAR Modeling Approach for Biscoumarin Derivatives
THT Phan, K Hengphasatporn, Y Shigeta, W Xie… - ACS …, 2023 - ACS Publications
Nineteen biscoumarins were synthesized, well-characterized, and evaluated against α-
glucosidases in vitro. Of these, six compounds (10, 12, 16, and 17–19) were newly …
glucosidases in vitro. Of these, six compounds (10, 12, 16, and 17–19) were newly …
Humic acid: A Biodegradable Organocatalyst for Solvent‐free Synthesis of Bis (indolyl) methanes, Bis (pyrazolyl) methanes, Bis‐coumarins and Bis‐lawsones
B Mitra, P Ghosh - ChemistrySelect, 2021 - Wiley Online Library
Humic acid, a biodegradable, non‐toxic and easily accessible high molecular weight
organocatalyst has been explored for the straightforward and environmentally benign …
organocatalyst has been explored for the straightforward and environmentally benign …
Toxicity of thimerosal in biological systems: Conformational changes in human hemoglobin, decrease of oxygen binding capacity, increase of protein glycation and …
M de Magalhães Silva, MD de Araújo Dantas… - International journal of …, 2020 - Elsevier
Thimerosal (TH), an organomercurial compound, is used as a preservative in vaccines and
cosmetics. Its interaction with human hemoglobin (Hb) was investigated under physiological …
cosmetics. Its interaction with human hemoglobin (Hb) was investigated under physiological …
Greener syntheses of coumarin derivatives using magnetic nanocatalysts: recent advances
S Zeinali, LZ Fekri, M Nikpassand… - Topics in Current …, 2023 - Springer
Abstract Coumarins (2 H-1-benzopyran-2-ones) are an important group of biological
heterocyclic compounds present in various parts of many plant species, encompassing an …
heterocyclic compounds present in various parts of many plant species, encompassing an …
4-Oxycoumarinyl linked acetohydrazide Schiff bases as potent urease inhibitors
Urease enzyme is responsible to catalyze the hydrolysis of urea into carbamate and
ammonia. Then carbamate hydrolyzed to ammonia and carbon dioxide. Excess release of …
ammonia. Then carbamate hydrolyzed to ammonia and carbon dioxide. Excess release of …
Design, synthesis, and evaluation of metronidazole-1, 2, 3-triazole derivatives as potent urease inhibitors
A new series of metronidazole-1, 2, 3-triazole derivatives 6a–o was synthesized and
evaluated as Helicobacter pylori urease inhibitors. All the synthesized compounds were …
evaluated as Helicobacter pylori urease inhibitors. All the synthesized compounds were …
Development of Urease Inhibitors by Fragment‐Based Dynamic Combinatorial Chemistry
Y Wu, S Zhao, C Liu, L Hu - ChemMedChem, 2022 - Wiley Online Library
In this study, fragment‐based dynamic combinatorial chemistry (DCC) was explored for the
development of novel urease inhibitors. Based on a rationally designed fragment, two …
development of novel urease inhibitors. Based on a rationally designed fragment, two …