A review on the structures and biological activities of anti-Helicobacter pylori agents

E Ghobadi, Z Ghanbarimasir, S Emami - European Journal of Medicinal …, 2021 - Elsevier
Helicobacter pylori is one of the main causal risk factor in the generation of chronic gastritis,
gastroduodenal ulcers and gastric carcinoma. Thus, the eradication of H. pylori infection is …

Determination of antioxidant, DNA protection, enzyme inhibition potential and molecular docking studies of a biomarker ursolic acid in Nepeta species

S Yenigün, Y Başar, Y İpek, L Behçet… - Journal of …, 2024 - Taylor & Francis
Ursolic acid (UA), which has many biological properties such as anti-cancer, anti-
inflammatory and antioxidant, and regulates some pharmacological processes, has been …

Anthraquinone Derivatives and Other Aromatic Compounds from Marine Fungus Asteromyces cruciatus KMM 4696 and Their Effects against Staphylococcus aureus

OI Zhuravleva, EA Chingizova, GK Oleinikova… - Marine Drugs, 2023 - mdpi.com
New anthraquinone derivatives acruciquinones A–C (1–3), together with ten known
metabolites, were isolated from the obligate marine fungus Asteromyces cruciatus KMM …

Exploring the chemical space of urease inhibitors to extract meaningful trends and drivers of activity

N Aniceto, VDB Bonifácio, RC Guedes… - Journal of Chemical …, 2022 - ACS Publications
Blocking the catalytic activity of urease has been shown to have a key role in different
diseases as well as in different agricultural applications. A vast array of molecules have …

Urease Inhibition and Structure‐Activity Relationship Study of Thiazolidinone‐, Triazole‐, and Benzothiazole‐Based Heterocyclic Derivatives: A Focus Review

R Singh, P Kumar, M Devi, J Sindhu, A Kumar… - …, 2023 - Wiley Online Library
Urease has a long and distinguished history in the development of enzymology since it was
the first enzyme crystallized by Sumner in 1926. The present review article is focused on the …

Ionic liquid-assisted synthesis of dihydropyrimidin (thi) one Biginelli adducts and investigation of their mechanism of urease inhibition

TC Braga, TF Silva, TMS Maciel, ECD da Silva… - New Journal of …, 2019 - pubs.rsc.org
Twenty-six Biginelli adducts were synthesized through an ionic liquid-assisted synthesis
with up to 92% yield. Sixteen of these Biginelli adducts were then assayed to determine their …

Inactivation of Jack Bean Urease by Nitidine Chloride from Zanthoxylum nitidum: Elucidation of Inhibitory Efficacy, Kinetics and Mechanism

Q Lu, D Tan, Y Xu, M Liu, Y He, C Li - Journal of Agricultural and …, 2021 - ACS Publications
Urease is a metalloenzyme that catalyzes the hydrolysis of urea into ammonia and carbon
dioxide, which has a negative impact on human health and agriculture. In this study, the …

A multi-biochemical and in silico study on anti-enzymatic actions of pyroglutamic acid against PDE-5, ACE, and urease using various analytical techniques …

M Šudomová, STS Hassan, H Khan, M Rasekhian… - Biomolecules, 2019 - mdpi.com
In the current study, pyroglutamic acid (pGlu), a natural amino acid derivative, has efficiently
inhibited the catalytic activities of three important enzymes, namely: Human recombinant …

Isoindolin-1-ones fused to barbiturates: from design and molecular docking to synthesis and urease inhibitory evaluation

H Kazemzadeh, E Hamidian, FS Hosseini, M Abdi… - ACS …, 2022 - ACS Publications
Helicobacter pylori-induced ulcers and gastric cancer have been one of the main obstacles
that the human community has ever struggled with, especially in recent decades. Several …

Design, synthesis, and evaluation of metronidazole-1, 2, 3-triazole derivatives as potent urease inhibitors

EB Rezaei, F Abedinifar, H Azizian, MN Montazer… - Chemical Papers, 2021 - Springer
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 …