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For: Aimene Y, Eychenne R, Rodriguez F, Mallet-ladeira S, Saffon-merceron N, Winum J, Nocentini A, Supuran CT, Benoist E, Seridi A. Synthesis, Crystal Structure, Inhibitory Activity and Molecular Docking of Coumarins/Sulfonamides Containing Triazolyl Pyridine Moiety as Potent Selective Carbonic Anhydrase IX and XII Inhibitors. Crystals 2021;11:1076. [DOI: 10.3390/cryst11091076] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
Number Citing Articles
1 Peerzada MN, Rizvi MA, Kk AK, Sahu A, Verma S. Nature-Based Computing Bioinformatics Approaches in Drug Discovery Against Promising Molecular Targets Carbonic Anhydrases and Serine/Threonine Kinases for Cancer Treatment. Nature-Inspired Intelligent Computing Techniques in Bioinformatics 2023. [DOI: 10.1007/978-981-19-6379-7_16] [Reference Citation Analysis]
2 Lengacher R, Marlin A, Śmiłowicz D, Boros E. Medicinal inorganic chemistry - challenges, opportunities and guidelines to develop the next generation of radioactive, photoactivated and active site inhibiting metal-based medicines. Chem Soc Rev 2022. [PMID: 35942718 DOI: 10.1039/d2cs00407k] [Reference Citation Analysis]
3 Tawfik HO, Shaldam MA, Nocentini A, Salem R, Almahli H, Al-Rashood ST, Supuran CT, Eldehna WM. Novel 3-(6-methylpyridin-2-yl)coumarin-based chalcones as selective inhibitors of cancer-related carbonic anhydrases IX and XII endowed with anti-proliferative activity. J Enzyme Inhib Med Chem 2022;37:1043-52. [PMID: 35437108 DOI: 10.1080/14756366.2022.2056734] [Cited by in F6Publishing: 1] [Reference Citation Analysis]