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For: Talebi M, Hamidian E, Niasari-naslaji F, Rahmani S, Hosseini FS, Boumi S, Montazer MN, Asadi M, Amanlou M. Synthesis, molecular docking, and biological evaluation of nitroimidazole derivatives as potent urease inhibitors. Med Chem Res 2021;30:1220-9. [DOI: 10.1007/s00044-021-02727-4] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
Number Citing Articles
1 Islam M, Khan A, Khan M, Halim SA, Ullah S, Hussain J, Al-harrasi A, Shafiq Z, Tasleem M, El-gokha A. Synthesis and biological evaluation of 2-nitrocinnamaldehyde derived thiosemicarbazones as urease inhibitors. Journal of Molecular Structure 2023;1284:135387. [DOI: 10.1016/j.molstruc.2023.135387] [Reference Citation Analysis]
2 Amini M, Abdel-jalil R, Moghadam ES, Al-sadi AM, Talebi M, Amanlou M, Shongwe M. Piperazine-based Semicarbazone Derivatives as Potent Urease Inhibitors: Design, Synthesis, and Bioactivity Screening. LDDD 2022;19:1111-1120. [DOI: 10.2174/1570180819666220405234009] [Reference Citation Analysis]
3 Song W, Liu M, Yuan L, Li S, Wang Y, Xiao Z, Zhu H. Synthesis, evaluation and mechanism exploration of 2-(N-(3-nitrophenyl)-N-phenylsulfonyl)aminoacetohydroxamic acids as novel urease inhibitors. Bioorganic & Medicinal Chemistry Letters 2022;78:129043. [DOI: 10.1016/j.bmcl.2022.129043] [Reference Citation Analysis]
4 Li S, Zhang Y, Wang Y, Yuan L, Kong C, Xiao Z, Zhu H. Identification of (N-aryl-N-arylsulfonyl)aminoacetohydroxamic acids as novel urease inhibitors and the mechanism exploration. Bioorganic Chemistry 2022. [DOI: 10.1016/j.bioorg.2022.106275] [Reference Citation Analysis]
5 Saeedian Moghadam E, Mohammed Al-sadi A, Ghafarzadegan R, Talebi M, Amanlou M, Amini M, Abdel-jalil R. Benzimidazole derivatives act as dual urease inhibitor and anti-helicobacter pylori agent; synthesis, bioactivity, and molecular docking study. Synthetic Communications. [DOI: 10.1080/00397911.2022.2061357] [Reference Citation Analysis]
6 Çapan İ. Methimazole Analogs as Urease Inhibitors: Synthesis, In Silico and In Vitro Evaluation. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202104076] [Reference Citation Analysis]
7 Saeedian Moghadam E, Al-Sadi AM, Talebi M, Amanlou M, Amini M, Abdel-Jalil R. Novel benzimidazole derivatives; synthesis, bioactivity and molecular docking study as potent urease inhibitors. Daru 2022;30:29-37. [PMID: 35040104 DOI: 10.1007/s40199-021-00427-3] [Reference Citation Analysis]
8 Saeedian Moghadam E, Al-sadi AM, Talebi M, Amanlou M, Amini M, Abdel-jalil R. 2-Aryl Benzimidazole Derivatives Act as Potent Urease Inhibitors; Synthesis, Bioactivity and Molecular Docking Study. Polycyclic Aromatic Compounds. [DOI: 10.1080/10406638.2021.2014534] [Reference Citation Analysis]
9 Saeedian Moghadam E, Al-sadi AM, Talebi M, Amanlou M, Amini M, Abdel-jalil R. Design, synthesis, and bioactivity investigation of novel benzimidazole derivatives as potent urease inhibitors. Synthetic Communications. [DOI: 10.1080/00397911.2021.2001661] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]