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Cited by in F6Publishing
For: Fiori-Duarte AT, Rodrigues RP, Kitagawa RR, Kawano DF. Insights into the Design of Inhibitors of the Urease Enzyme - A Major Target for the Treatment of Helicobacter pylori Infections. Curr Med Chem 2020;27:3967-82. [PMID: 30827224 DOI: 10.2174/0929867326666190301143549] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
Number Citing Articles
1 Cheok YY, Lee CYQ, Cheong HC, Vadivelu J, Looi CY, Abdullah S, Wong WF. An Overview of Helicobacter pylori Survival Tactics in the Hostile Human Stomach Environment. Microorganisms 2021;9:2502. [PMID: 34946105 DOI: 10.3390/microorganisms9122502] [Reference Citation Analysis]
2 Masetti M, Falchi F, Gioia D, Recanatini M, Ciurli S, Musiani F. Targeting the Protein Tunnels of the Urease Accessory Complex: A Theoretical Investigation. Molecules 2020;25:E2911. [PMID: 32599898 DOI: 10.3390/molecules25122911] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
3 Šudomová M, Hassan STS. Gossypol from Gossypium spp. Inhibits Helicobacter pylori Clinical Strains and Urease Enzyme Activity: Bioactivity and Safety Assessments. Sci Pharm 2022;90:29. [DOI: 10.3390/scipharm90020029] [Reference Citation Analysis]
4 Kazemzadeh H, Hamidian E, Hosseini FS, Abdi M, Niasari Naslaji F, Talebi M, Asadi M, Biglar M, Zarei I, Amanlou M. Isoindolin-1-ones Fused to Barbiturates: From Design and Molecular Docking to Synthesis and Urease Inhibitory Evaluation. ACS Omega 2022;7:19401-11. [DOI: 10.1021/acsomega.2c01028] [Reference Citation Analysis]
5 Lu Q, Zhang Z, Xu Y, Chen Y, Li C. Sanguinarine, a major alkaloid from Zanthoxylum nitidum (Roxb.) DC., inhibits urease of Helicobacter pylori and jack bean: Susceptibility and mechanism. J Ethnopharmacol 2022;:115388. [PMID: 35577159 DOI: 10.1016/j.jep.2022.115388] [Reference Citation Analysis]
6 Milo S, Heylen RA, Glancy J, Williams GT, Patenall BL, Hathaway HJ, Thet NT, Allinson SL, Laabei M, Jenkins ATA. A small-molecular inhibitor against Proteus mirabilis urease to treat catheter-associated urinary tract infections. Sci Rep 2021;11:3726. [PMID: 33580163 DOI: 10.1038/s41598-021-83257-2] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
7 Ji J, Wang S, Zhao J, Yang T, Wang J, You Z. Synthesis, crystal structures and urease inhibition of copper, nickel and zinc complexes derived from 4-chloro-2-((pyridin-2-ylmethylene)amino)phenol. Journal of Coordination Chemistry. [DOI: 10.1080/00958972.2022.2032005] [Reference Citation Analysis]