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Marouan Rami | doi.page

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Marouan Rami

Inserm(FR)Université de Lille(FR)Centre Hospitalier Universitaire de Lille(FR)Lille Neurosciences & Cognition

Publications by Year

Research Areas

Enzyme function and inhibition, Synthesis and Catalytic Reactions, Cholinesterase and Neurodegenerative Diseases, Chemical Reactions and Mechanisms, Circadian rhythm and melatonin

Most-Cited Works

→ Carbonic anhydrase IX: A new druggable target for the design of antitumor agents(2007)242 cited
→ Carbonic Anhydrase Inhibitor Coated Gold Nanoparticles Selectively Inhibit the Tumor-Associated Isoform IX over the Cytosolic Isozymes I and II(2008)110 cited
→ Targeting carbonic anhydrase IX by nitroimidazole based sulfamides enhances the therapeutic effect of tumor irradiation: A new concept of dual targeting drugs(2013)92 cited
→ Hypoxia-Targeting Carbonic Anhydrase IX Inhibitors by a New Series of Nitroimidazole-Sulfonamides/Sulfamides/Sulfamates(2013)90 cited
→ Carbonic anhydrase inhibitors: Copper(II) complexes of polyamino-polycarboxylamido aromatic/heterocyclic sulfonamides are very potent inhibitors of the tumor-associated isoforms IX and XII(2007)38 cited
→ Design, synthesis and pharmacological evaluation of new series of naphthalenic analogues as melatoninergic (MT1/MT2) and serotoninergic 5-HT2C dual ligands (I)(2012)34 cited

→ Carbonic anhydrase inhibitors: 2-Substituted-1,3,4-thiadiazole-5-sulfamides act as powerful and selective inhibitors of the mitochondrial isozymes VA and VB over the cytosolic and membrane-associated carbonic anhydrases I, II and IV(2008)30 cited

→ Carbonic Anhydrase Inhibitors: Design of Membrane‐Impermeant Copper(II) Complexes of DTPA‐, DOTA‐, and TETA‐Tailed Sulfonamides Targeting the Tumor‐Associated Transmembrane Isoform IX(2008)28 cited

→ Synthesis and biological evaluation of new naphtho- and quinolinocyclopentane derivatives as potent melatoninergic (MT 1 /MT 2 ) and serotoninergic (5-HT 2C ) dual ligands(2017)16 cited

→ Sulfonamides incorporating boroxazolidone moieties are potent inhibitors of the transmembrane, tumor-associated carbonic anhydrase isoforms IX and XII(2011)16 cited