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3-amino-3,4-dihydro-2H-1-benzopyran derivatives as 5-HT1A receptor ligands and potential anxiolytic agents. 2. Synthesis and quantitative structure-activity relationship studies of spiro[pyrrolidine- and piperidine-2,3'(2'H)-benzopyrans].
Comoy C, Marot C, Podona T, Baudin ML, Morin-Allory L, Guillaumet G, Pfeiffer B, Caignard DH, Renard P, Rettori MC, Adam G, Guardiola-Lemaitre B. Comoy C, et al. Among authors: podona t. J Med Chem. 1996 Oct 11;39(21):4285-98. doi: 10.1021/jm950861w. J Med Chem. 1996. PMID: 8863806
4H-1,2,4-Pyridothiadiazine 1,1-dioxides and 2,3-dihydro-4H-1,2, 4-pyridothiadiazine 1,1-dioxides chemically related to diazoxide and cyclothiazide as powerful positive allosteric modulators of (R/S)-2-amino-3-(3-hydroxy-5-methylisoxazol-4-yl)propionic acid receptors: design, synthesis, pharmacology, and structure-activity relationships.
Pirotte B, Podona T, Diouf O, de Tullio P, Lebrun P, Dupont L, Somers F, Delarge J, Morain P, Lestage P, Lepagnol J, Spedding M. Pirotte B, et al. Among authors: podona t. J Med Chem. 1998 Jul 30;41(16):2946-59. doi: 10.1021/jm970694v. J Med Chem. 1998. PMID: 9685234
3-and 4-substituted 4H-pyrido[4,3-e]-1,2,4-thiadiazine 1,1-dioxides as potassium channel openers: synthesis, pharmacological evaluation, and structure-activity relationships.
de Tullio P, Pirotte B, Lebrun P, Fontaine J, Dupont L, Antoine MH, Ouedraogo R, Khelili S, Maggetto C, Masereel B, Diouf O, Podona T, Delarge J. de Tullio P, et al. Among authors: podona t. J Med Chem. 1996 Feb 16;39(4):937-48. doi: 10.1021/jm9500582. J Med Chem. 1996. PMID: 8632417
Brevetoxin derivatives that inhibit toxin activity.
Purkerson-Parker SL, Fieber LA, Rein KS, Podona T, Baden DG. Purkerson-Parker SL, et al. Among authors: podona t. Chem Biol. 2000 Jun;7(6):385-93. doi: 10.1016/s1074-5521(00)00119-8. Chem Biol. 2000. PMID: 10873835