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See detailRelaxant effects on the rat uterine smooth muscle of putative K+ATP channel openers
Boverie, S.; De Tullio, Pascal ULg; Sebille, S. et al

Poster (2004, July)

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See detailSynthèse de nouveaux analogues benzothiadiaziniques en tant qu’activateurs potentiels des canaux KATP et leur évaluation pharmacologique in vitro sur cellules B pancréatiques, aorte et utérus de rats
Boverie, S.; Antoine, M. H.; De Tullio, Pascal ULg et al

Poster (2004, June)

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See detailPyridinic sulfonamides as potential COX-2 inhibitors
Julemont, F.; De Leval, X.; Damas, J. et al

Poster (2003, May)

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See detailRelaxant effects on the rat uterine smooth muscle of K+ATP channel openers compared to ritodrine, diltiazem and verapamil : development of new pharmacological in vitro models
Boverie, S.; De Tullio, Pascal ULg; Dewalque, D. et al

Poster (2002, September)

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See detailRelaxant effect of K+ATP channel openers on the uterine smooth muscle: pharmacological in vitro models
De Tullio, Pascal ULg; Boverie, S.; Dewalque, D. et al

Conference (2002, March 02)

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See detailRelaxant effect of K+ATP channel openers on the uterine smooth muscle: pharmacological in vitro models
De Tullio, Pascal ULg; Boverie, S.; Dewalque, D. et al

Poster (2002, March 02)

See detailAction myorelâchante sur la fibre musculaire lisse utérine de nouveaux dérivés de type 4H-1,2,4-benzothiadiazine 1,1-dioxyde diversement substitués en position 3 et 7
Boverie, S.; Dewalque, D.; Sebille, S. et al

Conference (2002, January 25)

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See detailSpectral and crystallographic study of pyridinic analogues of nimesulide : determination of the active form of methanesulfonamides as COX-2 selective inhibitors
Julémont, F.; de Leval, X.; Michaux, C. et al

in Journal of Medicinal Chemistry (2002), 45

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See detailSpectral and crystallographic study of pyridinic analogues of nimesulide : determination of the active form of methanesulfonamides as COX-2 selective inhibitors
Julémont, F.; De Leval, X.; Michaux, C. et al

in Journal of Medicinal Chemistry (2002)

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See detailRelaxant effect of K+ATP channel openers on the uterine smooth muscle; phrmacological in vitro models
De Tullio, Pascal ULg; Boverie, S.; Dewalque, D. et al

in Fundamental & Clinical Pharmacology (2002)

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See detailPropriétés biologiques des 7-chloro-4H-1,2,4-benzothiadiazine 1,1-dioxydes diversement substitués en position 3: nouveaux analogues du diazoxide
Boverie, S.; De Tullio, Pascal ULg; Becker, B. et al

Poster (2001, June 01)

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See detailPreparation and biological properties of chemically diverse 3-substituted 7-chloro-4H-1,2,4-benzothiadiazine 1,1-dioxides structurally related to the potassium channel opener diazoxide
Boverie, S.; De Tullio, Pascal ULg; Becker, B. et al

Conference (2001, May)

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See detailOriginal 2-alkylamino-6-halogenoquinazolin-4(3H)-ones and KATP channel activity
Somers, F.; Ouedraogo, R.; Antoine, M.-H. et al

in Journal of Medicinal Chemistry (2001), 44

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See detailNew 3-alkylamino-7-chloro-4H-1,2,4-benzothiadiazine 1,1-dioxides related to BPDZ 73 as putative KATP channel openers: design, synthesis and pharmacological evaluation
Boverie, S.; Becker, B.; Somers, F. et al

Poster (2000, December 01)

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See detailHeart rate decrease induced by BPDZ 259, a diazoxide analogue
Damas, J.; Pirotte, Bernard ULg

Poster (2000, November 18)

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See detailSynthesis and biological evaluation of 3-alkylamino-7-chloro-4H-1,2,4-benzothiadiazine 1,1-dioxides as KATP channel openers structurally related to BPDZ 73
Boverie, S.; Becker, B.; Somers, F. et al

Poster (2000, September)

See detailEvaluation de la selectivité COX-1/COX-2 de drogues à visée anti-inflammatoire sur sang humain
De Leval, X.; Delarge, J.; Devel, P. et al

Poster (2000, May)

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See detailPharmacological evaluation of original sulfonylureas as thromboxane A2 antagonists
Dogne, J. M.; De Leval, X.; Neven, P. et al

Poster (2000, March 04)

See detailEvaluation of classical NSAIDs in a model of human whole blood assay
De Leval, X.; Delarge, J.; Devel, P. et al

Poster (2000, March 04)

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See detailLes 3-alkylsulfanyl- et 3-alkoxy-4H-1,2,4-benzothiadiazine 1,1-dioxydes structuralement apparentés aux 3-alkylamino-4H-1,2,4-benzothiadiazine 1,1-dioxydes en tant qu’activateurs potentiels des canaux potassiques sensibles à l’ATP
Boverie, S.; De Tullio, Pascal ULg; Ouedraogo, R. et al

Poster (2000, January 28)