Tchao Podona

Circumvention of P-GP MDR as a Function of Anthracycline Lipophilicity and Charge

Théodore J. Lampidis, Despina S. Kolonias, Tchao Podona et al. · Biochemistry · 1997 · 68 citations

P-gp Mdr, Mdr Recognition, Antimicrobial Chemotherapy +16

4<i>H</i>-1,2,4-Pyridothiadiazine 1,1-Dioxides and 2,3-Dihydro-4<i>H</i>-1,2,4-pyridothiadiazine 1,1-Dioxides Chemically Related to Diazoxide and Cyclothiazide as Powerful Positive Allosteric Modulators of (<i>R</i>/<i>S</i>)-2-Amino-3-(3-hydroxy-5-methylisoxazol-4-yl)propionic Acid Receptors:  Design, Synthesis, Pharmacology, and Structure−Activity Relationships

Bernard Pirotte, Tchao Podona, Ousmane Diouf et al. · Journal of Medicinal Chemistry · 1998 · 60 citations

Ampa Receptor Modulator, Pharmacotherapy, Chemistry +19

3- and 4-Substituted 4<i>H</i>-Pyrido[4,3-<i>e</i>]-1,2,4-thiadiazine 1,1-Dioxides as Potassium Channel Openers:  Synthesis, Pharmacological Evaluation, and Structure−Activity Relationships

Pascal De Tullio, Bernard Pirotte, Philippe Lebrun et al. · Journal of Medicinal Chemistry · 1996 · 57 citations

3,4-Dihydro-3-amino-2H-1-benzopyran Derivatives as 5-HT1A Receptor Ligands and Potential Anxiolytic Agents. 1. Synthesis and Structure-Activity Relationship Studies

Tchao Podona, Béatrice Guardiola‐Lemaître, Daniel‐Henri Caignard et al. · Journal of Medicinal Chemistry · 1994 · 50 citations · Full text

Brevetoxin derivatives that inhibit toxin activity

Sherry L Purkerson-Parker, Lynne A. Fieber, Kathleen S. Rein et al. · Chemistry & Biology · 2000 · 45 citations · Full text

Toxinology, Biochemistry, Medicine +4