Novel N,N-dimethylbarbituric-pyridinium derivatives as potent urease inhibitors: Synthesis, in vitro, and in silico studies-Reference-Cited by-同舟云学术

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

Published:2020-01 Issue: Volume:95 Page:103529
ISSN:0045-2068
Container-title:Bioorganic Chemistry
language:en
Short-container-title:Bioorganic Chemistry

Author:

Biglar Mahmood,Mirzazadeh Roghieh,Asadi Mehdi,Sepehri Saghi,Valizadeh Yousef,Sarrafi Yaghoub,Amanlou Massoud,Larijani Bagher,Mohammadi-Khanaposhtani Maryam,Mahdavi Mohammad

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry

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5. Design, synthesis, in vitro evaluation, molecular docking and ADME properties studies of hybrid bis-coumarin with thiadiazole as a new inhibitor of Urease;Alomari;Bioorg. Chem.,2019

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1. In vitro anti-Helicobacter pylori, anti-urease and anti-gastric cancer activities of novel hydrazones;Journal of Molecular Structure;2024-07

2. Design, synthesis, in vitro urease inhibitory potentials and in silico molecular docking study of benzimidazole bearing thiosemicarbazides/sulfonamide Analogues;Journal of Molecular Structure;2024-01

3. Inhibition of ureases: studies and applications;Ureases;2024

4. Synthesis of Some Benzimidazole-Thiophene Hybrids as Potential Urease and Lipase Inhibitors;Russian Journal of Bioorganic Chemistry;2023-11

5. An overview of the privileged synthetic heterocycles as urease enzyme inhibitors: Structure–activity relationship;Archiv der Pharmazie;2023-07-03