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Novel 3-Sulfonamide Dual-Tail Pyrrol-2-one Bridged Molecules as Potent Human Carbonic Anhydrase Isoform Inhibitors: Design, Synthesis, Molecular Modeling Investigation, and Anticancer Activity in MeWo, SK-BR-3, and MG-63 Cell Lines.
Al-Matarneh CM, Simionescu N, Nicolescu A, Silion M, Angeli A, Paoletti N, Bonardi A, Gratteri P, Pinteala M, Supuran CT. Al-Matarneh CM, et al. Among authors: supuran ct. J Med Chem. 2025 Jan 10. doi: 10.1021/acs.jmedchem.4c02586. Online ahead of print. J Med Chem. 2025. PMID: 39793971
Depsides from Origanum dictamnus and Satureja pilosa as selective inhibitors of carbonic anhydrases: Isolation, structure elucidation, X-ray crystallography.
Paloukopoulou C, Ntagli OS, Gherardi L, Dourdouni V, Filippou G, Alterio V, Giovannuzzi S, Massardi ML, De Simone G, Ronca R, Supuran CT, Pescitelli G, Karioti A. Paloukopoulou C, et al. Among authors: supuran ct. Arch Pharm (Weinheim). 2025 Jan;358(1):e2400823. doi: 10.1002/ardp.202400823. Arch Pharm (Weinheim). 2025. PMID: 39711099
New 7-hydroxycoumarin acetamide derivatives as human carbonic anhydrase IX and XII inhibitors: Design, synthesis, biological evaluation and molecular docking studies.
Maddipatla S, Bakchi B, Shinde MA, Bonardi A, Raman PK, Bhalerao HA, Singampalli A, Nanduri S, Godugu C, Sonti R, Supuran CT, Yaddanapudi VM. Maddipatla S, et al. Among authors: supuran ct. Arch Pharm (Weinheim). 2025 Jan;358(1):e2400482. doi: 10.1002/ardp.202400482. Arch Pharm (Weinheim). 2025. PMID: 39686882
2,092 results