[HTML][HTML] Flavonoids and related privileged scaffolds as potential urease inhibitors: a review

MM Al-Rooqi, EU Mughal, QA Raja, EM Hussein… - RSC …, 2023 - pubs.rsc.org
Infections caused by bacteria are a significant issue on a global scale, and imperative action
is required to discover novel or improved therapeutic agents. Flavonoids are a class of plant …

An overview: metal-based inhibitors of urease

W Yang, Z Peng, G Wang - Journal of Enzyme Inhibition and …, 2023 - Taylor & Francis
Urease is a kind of nickel-dependent metalloenzyme, which exists in the biological world
widely, and can catalyse the hydrolysis of urea into ammonia and carbon dioxide to provide …

[HTML][HTML] Phenolic profiles, antioxidant, antiquorum sensing, antibiofilm and enzyme inhibitory activities of selected Acacia species collected from Benin

KY Alain, AN Tamfu, S Kucukaydin, O Ceylan… - LWT, 2022 - Elsevier
Gum arabica is a local commercial nutraceutical and food preservative collected mostly from
acacia plants. HPLC-DAD analysis identified gallic acid, syringic acid, ferulic acid, coumarin …

[HTML][HTML] Inhibitory activity of catecholic phosphonic and phosphinic acids against Helicobacter pylori ureolysis

M Maślanka, W Tabor, P Krzyżek… - European Journal of …, 2023 - Elsevier
Catechols have been reported to be potent covalent inhibitors of ureases, and they exhibit
activity by modifying cysteine residues at the entrance to enzymatic active sites. Following …

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 …

Synergizing structure and function: Cinnamoyl hydroxamic acids as potent urease inhibitors

LPS Viana, GM Naves, IG Medeiros, AS Guimarães… - Bioorganic …, 2024 - Elsevier
The current investigation encompasses the structural planning, synthesis, and evaluation of
the urease inhibitory activity of a series of molecular hybrids of hydroxamic acids and …

Chalcones bearing nitrogen‐containing heterocyclics as multi‐targeted inhibitors: Design, synthesis, biological evaluation and molecular docking studies

Y Sıcak, H Kekeçmuhammed… - Journal of Molecular …, 2023 - Wiley Online Library
In this work, a series of chalcones (1a–d, 2a–d, 3a–d, 4a–d, and 5a–d) were designed and
synthesized by Claisen–Schmidt condensation. Also, their chemical structures were …

[HTML][HTML] In vitro evaluation of novel mefenamic acid derivatives as potential α-glucosidase and urease inhibitors: Design, synthesis, in silico and cytotoxic studies

S Daud, W Rehman, M Niaz, A Sardar… - Journal of Saudi …, 2023 - Elsevier
This study aim to synthesize new 1, 3, 4-oxadiazole derivatives incorporating mefenamic
acid as promising α-glucosidase and urease inhibitors, potentially leading to the treatment of …

DNA protection, molecular docking, enzyme inhibition and enzyme kinetic studies of 1,5,9-epideoxyloganic acid isolated from Nepeta aristata with bio-guided …

Y Başar, S Yenigün, Y İpek, L Behçet… - Journal of …, 2023 - Taylor & Francis
epideoxyloganic acid (ELA) was isolated from the aerial parts of endemic Nepeta aristata
Boiss Et Kotschy Ex Boiss crude extract (methanol: chloroform) using silica gel (hexane …

Unusual short intramolecular N–H⋅⋅⋅ H–C contact and weak intermolecular interactions in two N-(adamantan-1-yl) piperazine carbothioamides: Crystallography …

LH Al-Wahaibi, S Mangaiyarkarasi, O Blacque… - Journal of Molecular …, 2023 - Elsevier
Crystal structures of two closely related N-(adamantan-1-yl) piperazine carbothioamides
have been examined in detail using the Hirshfeld surface, fingerprint analysis, PIXEL energy …