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See detail3-Alkylamino-4H-1,2,4-benzothiadiazine 1,1-dioxides as ATP-sensitive potassium channel openers : effect of 6,7-distribution on potency and tissue selectivity
De Tullio, Pascal ULiege; Boverie, S.; Becker, B. et al

in Journal of Medicinal Chemistry (2005), 48

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See detailSynthesis and characterisation of a quinolinonic compound activating ATP-sensitive K+ channels in endocrine and smooth muscle tissues
Becker, B.; Antoine, M.-H.; Nguyen, Q.-A. et al

in British Journal of Pharmacology (2001), 134

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See detailA potent diazoxide analogue activating ATP-sensitive K+ channels and inhibiting insulin release
Lebrun, P.; Arkhammar, P.; Antoine, M.-H. et al

in Diabetologia (2000), 43

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See detailPharmacological evaluation of 3-alkylsulfanyl-4H-1,2,4-benzothiadiazine 1,1-dioxides structurally related to the KATP channel opener diazoxide
Boverie, S.; Nguyen, Q.-A.; De Tullio, Pascal ULiege et al

in Fundamental & Clinical Pharmacology (1999), 13

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See detailIn vivo et in vitro effect of new glibenclamide isosteres
Lebrun, P.; Ouedraogo, R.; Nguyen, Q.-A. et al

in Fundamental & Clinical Pharmacology (1999), 13, Suppl. 1

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See detailSynthesis and pharmacological evaluation of KATP-channel openers related to cromakalim: introduction of arylsulphonylurea moieties
Khelili, S.; Nguyen, Q.-A.; Lebrun, P. et al

in Pharmacy and Pharmacology Communications (1999), 5

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See detailPharmacological study of original 3-alkylamino-2-methyl-2H-pyrido[4,3-e]-1,2,4-thiadiazine 1,1-dioxides
Ouedraogo, R.; Nguyen, Q.-A.; Antoine, M.-H. et al

in Fundamental & Clinical Pharmacology (1999), 13

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