Identification of (N-aryl-N-arylsulfonyl)aminoacetohydroxamic acids as novel urease inhibitors and the mechanism exploration.

[1]  Dong-dong Li,et al.  Design, synthesis, and biological activity of 9-O-cinnamoylberberines as novel lipid-lowering agents. , 2022, Natural product research.

[2]  Houman Kazemzadeh,et al.  Isoindolin-1-ones Fused to Barbiturates: From Design and Molecular Docking to Synthesis and Urease Inhibitory Evaluation , 2022, ACS omega.

[3]  Dong-dong Li,et al.  Discovery and structural optimization of 9-O-phenylsulfonyl-berberines as new lipid-lowering agents. , 2022, Bioorganic chemistry.

[4]  B. Larijani,et al.  Design and synthesis of novel nitrothiazolacetamide conjugated to different thioquinazolinone derivatives as anti-urease agents , 2022, Scientific Reports.

[5]  İrfan Çapan,et al.  Methimazole Analogs as Urease Inhibitors: Synthesis, In Silico and In Vitro Evaluation , 2022, ChemistrySelect.

[6]  Z. You,et al.  Synthesis, crystal structures and urease inhibition of copper, nickel and zinc complexes derived from 4-chloro-2-((pyridin-2-ylmethylene)amino)phenol , 2022, Journal of Coordination Chemistry.

[7]  B. Larijani,et al.  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. , 2022, Bioorganic chemistry.

[8]  W. Song,et al.  Recent Efforts in the Discovery of Urease Inhibitor Identifications. , 2021, Current topics in medicinal chemistry.

[9]  Mubashir Hassan,et al.  Exploring Amantadine Derivatives as Urease Inhibitors: Molecular Docking and Structure–Activity Relationship (SAR) Studies , 2021, Molecules.

[10]  D. Tan,et al.  Inactivation of Jack Bean Urease by Nitidine Chloride from Zanthoxylum nitidum: Elucidation of Inhibitory Efficacy, Kinetics and Mechanism. , 2021, Journal of agricultural and food chemistry.

[11]  Medha J. Gunaratna,et al.  Synthesis, In Silico Studies, and Evaluation of Syn and Anti Isomers of N-Substituted Indole-3-carbaldehyde Oxime Derivatives as Urease Inhibitors against Helicobacter pylori , 2021, Molecules.

[12]  H. Ouyang,et al.  Synthesis and Biological Evaluation of Dithiobisacetamides as Novel Urease Inhibitors , 2021, ChemMedChem.

[13]  M. Ali,et al.  Zenkeramide: a new iso-benzofuranone propanamide and urease inhibitory constituents of Celtis zenkeri Engl stem bark (Ulmaceae) , 2021, Natural product research.

[14]  S. Emami,et al.  A review on the structures and biological activities of anti-Helicobacter pylori agents. , 2021, European journal of medicinal chemistry.

[15]  A. Rehman,et al.  N-Aryl-3,4-dihydroisoquinoline Carbothioamide Analogues as Potential Urease Inhibitors , 2021, ACS omega.

[16]  John F. Trant,et al.  New isolate from Salvinia molesta with antioxidant and urease inhibitory activity , 2021, Drug development research.

[17]  U. Farooq,et al.  Design and synthesis of thiobarbituric acid analogues as potent urease inhibitors , 2021 .

[18]  K. Richards,et al.  Development of One-Step Non-Solvent Extraction and Sensitive UHPLC-MS/MS Method for Assessment of N-(n-Butyl) Thiophosphoric Triamide (NBPT) and N-(n-Butyl) Phosphoric Triamide (NBPTo) in Milk , 2021, Molecules.

[19]  S. Rahmani,et al.  Synthesis, molecular docking, and biological evaluation of nitroimidazole derivatives as potent urease inhibitors , 2021, Medicinal Chemistry Research.

[20]  Łukasz Berlicki,et al.  Covalent Inhibition of Bacterial Urease by Bifunctional Catechol-Based Phosphonates and Phosphinates. , 2020, Journal of medicinal chemistry.

[21]  Zhenzhong Wang,et al.  Discovery of 7,9-Disulfatetrahydroberberine as Novel Lipid-Lowering Agents , 2020, ACS omega.

[22]  L. Mazzei,et al.  Inhibition of urease, a Ni-enzyme: the reactivity of a key thiol with mono- and di-substituted catechols elucidated by kinetic, structural and theoretical studies. , 2020, Angewandte Chemie.

[23]  Zhenzhong Wang,et al.  Berberine: a Promising Natural Isoquinoline Alkaloid for Development of Hypolipidemic Drug. , 2020, Current topics in medicinal chemistry.

[24]  H. Ouyang,et al.  N-monosubstituted thiosemicarbazide as novel Ure inhibitors: synthesis, biological evaluation and molecular docking. , 2020, Future medicinal chemistry.

[25]  Li Liu,et al.  Synthesis and Structure-Activity Relationship Studies of N-monosubstituted Aroylthioureas as Urease Inhibitors. , 2020, Medicinal chemistry (Shariqah (United Arab Emirates)).

[26]  D. Kumaragamage,et al.  Efficiency of fall versus spring applied urea‐based fertilizers treated with urease and nitrification inhibitors II. Crop yield and nitrogen use efficiency , 2020 .

[27]  Zaheer Ul-Haq,et al.  Development of sulfonamide-based Schiff bases targeting urease inhibition: Synthesis, characterization, inhibitory activity assessment, molecular docking and ADME studies. , 2020, Bioorganic chemistry.

[28]  Zhenzhong Wang,et al.  Molecular Dynamics Analysis of Binding Sites of Epidermal Growth Factor Receptor Kinase Inhibitors , 2020, ACS omega.

[29]  X. Pan,et al.  N-monoarylacetothioureas as potent urease inhibitors: synthesis, SAR, and biological evaluation , 2019, Journal of enzyme inhibition and medicinal chemistry.

[30]  A. Saeed,et al.  Robust therapeutic potential of carbazole-triazine hybrids as a new class of urease inhibitors: A distinctive combination of nitrogen-containing heterocycles. , 2019, Bioorganic chemistry.

[31]  A. Saeed,et al.  Developing new hybrid scaffold for urease inhibition based on carbazole-chalcone conjugates: Synthesis, assessment of therapeutic potential and computational docking analysis. , 2019, Bioorganic & medicinal chemistry.

[32]  P. Berben,et al.  Use of a urease inhibitor to mitigate ammonia emissions from urine patches , 2019, Environmental technology.

[33]  L. Mazzei,et al.  The Structure of the Elusive Urease-Urea Complex Unveils the Mechanism of a Paradigmatic Nickel-Dependent Enzyme. , 2019, Angewandte Chemie.

[34]  A. Wadood,et al.  Atenolol thiourea hybrid as potent urease inhibitors: Design, biology-oriented drug synthesis, inhibitory activity screening, and molecular docking studies. , 2019, Bioorganic chemistry.

[35]  Shen-Zhen Ren,et al.  Arylamino containing hydroxamic acids as potent urease inhibitors for the treatment of Helicobacter pylori infection. , 2018, European journal of medicinal chemistry.

[36]  H. Ouyang,et al.  The synthesis and evaluation of phenoxyacylhydroxamic acids as potential agents for Helicobacter pylori infections. , 2018, Bioorganic & medicinal chemistry.

[37]  Weiwei Ni,et al.  Resolution and evaluation of 3‐chlorophenyl‐3‐hydroxypropionylhydroxamic acid as antivirulence agent with excellent eradication efficacy in Helicobacter pylori infected mice , 2018, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

[38]  Shovan Mondal,et al.  Synthesis of a Series of 2‐Aminodiarylsulfones by Brønsted Acid Mediated Regioselective Fries Type Rearrangement of N‐Alkyl‐N ‐arylbenzenesulfonamides , 2018 .

[39]  Hong-yu Zhang,et al.  3-Arylpropionylhydroxamic acid derivatives as Helicobacter pylori urease inhibitors: Synthesis, molecular docking and biological evaluation. , 2016, Bioorganic & medicinal chemistry.

[40]  N. Abbas,et al.  Structurally Diversified Heterocycles and Related Privileged Scaffolds as Potential Urease Inhibitors: A Brief Overview , 2013, Archiv der Pharmazie.

[41]  Jing-Jun Dong,et al.  Synthesis, structure-activity relationship analysis and kinetics study of reductive derivatives of flavonoids as Helicobacter pylori urease inhibitors. , 2013, European journal of medicinal chemistry.

[42]  R. Uddin,et al.  Synthesis, antioxidant activities and urease inhibition of some new 1,2,4-triazole and 1,3,4-thiadiazole derivatives. , 2010, European journal of medicinal chemistry.

[43]  Yasuko Takahashi,et al.  Synthesis of biotinylated photoaffinity probes based on arylsulfonamide γ-secretase inhibitors , 2006 .

[44]  M. W. Weatherburn Phenol-hypochlorite reaction for determination of ammonia , 1967 .