An overview on the synthetic urease inhibitors with structure-activity relationship and molecular docking

W Yang, Q Feng, Z Peng, G Wang - European Journal of Medicinal …, 2022 - Elsevier
Urease is a kind of enzyme which could be found in various bacteria, fungi, plants, and
algae, which can quickly catalyze the hydrolysis of urea into ammonia and carbon dioxide …

Recent efforts in the discovery of urease inhibitor identifications

WQ Song, ML Liu, SY Li, ZP Xiao - Current Topics in Medicinal …, 2022 - ingentaconnect.com
Urease is an attractive drug target for designing anti-infective agents against pathogens
such as Helicobacter pylori, Proteus mirabilis, and Ureaplasma urealyticum. In the past …

Design and synthesis of novel nitrothiazolacetamide conjugated to different thioquinazolinone derivatives as anti-urease agents

M Sohrabi, M Nazari Montazer, SM Farid, N Tanideh… - Scientific Reports, 2022 - nature.com
The present article describes the design, synthesis, in vitro urease inhibition, and in silico
molecular docking studies of a novel series of nitrothiazolacetamide conjugated to different …

[HTML][HTML] Phytochemical analysis, UPLC-ESI-Orbitrap-MS analysis, biological activity, and toxicity of extracts from Tripleurospermum limosum (Maxim.) Pobed

M Chen, X He, H Sun, Y Sun, L Li, J Zhu, G Xia… - Arabian Journal of …, 2022 - Elsevier
Tripleurospermum limosum (TL) has been used in folk medicine to treat gastritis. Toward the
further development and use of TL, we report the phytochemical profiling, determination of …

Design and synthesis of new N-thioacylated ciprofloxacin derivatives as urease inhibitors with potential antibacterial activity

K Pedrood, H Azizian, MN Montazer, A Moazzam… - Scientific Reports, 2022 - nature.com
A new series of N-thioacylated ciprofloxacin 3a–n were designed and synthesized based on
Willgerodt–Kindler reaction. The results of in vitro urease inhibitory assay indicated that …

[HTML][HTML] [1, 2, 4] triazolo [3, 4-b][1, 3, 4] thiadiazole derivatives as new therapeutic candidates against urease positive microorganisms: design, synthesis …

MK Ghomi, M Noori, MN Montazer… - Scientific …, 2023 - ncbi.nlm.nih.gov
Regarding the important role of the urease enzyme as a virulence factor in urease-positive
microorganisms in this study, new series of [1, 2, 4] triazolo [3, 4-b][1, 3, 4] thiadiazole …

Synthesis and in vitro urease inhibitory activity of 5-nitrofuran-2-yl-thiadiazole linked to different cyclohexyl-2-(phenylamino) acetamides, in silico and kinetic studies

M Asadi, A Iraji, M Sherafati, MN Montazer, S Ansari… - Bioorganic …, 2022 - Elsevier
Abstract A series of 5-nitrofuran-2-yl-thiadiazole linked to different cyclohexyl-2-
(phenylamino) acetamides were rationally designed and synthesized. All synthetic …

Different barbiturate derivatives linked to aryl hydrazone moieties as urease inhibitors; design, synthesis, urease inhibitory evaluations, and molecular dynamic …

M Mollazadeh, H Azizian, A Fakhrioliaei, A Iraji… - Medicinal Chemistry …, 2023 - Springer
New series of barbiturates linked to aryl hydrazone derivatives 4a-n were designed and
synthesized. Briefly, aniline derivatives in the presence of HBF4 and NaNO2 convert to aryl …

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 …

Novel phenylurea-pyridinium derivatives as potent urease inhibitors: Synthesis, in vitro, and in silico studies

SE Sadat-Ebrahimi, A Bigdelou, RH Sooreshjani… - Journal of Molecular …, 2022 - Elsevier
Urease is known as a virulence factor of some pathogen in the living organism. In this study,
a novel series of phenylurea conjugated to different alkyl pyridinium were designed …