Khelili S, de Tullio P, Lebrun P, Fillet M, Antoine M H, Ouedraogo R, Dupont L, Fontaine J, Felekidis A, Leclerc G, Delarge J, Pirotte B
Laboratoire de Chimie Pharmaceutique, Institut de Pharmacie, Université Liège, Belgium.
Bioorg Med Chem. 1999 Aug;7(8):1513-20. doi: 10.1016/s0968-0896(99)00082-6.
The preparation and the pharmacological evaluation of the R- and S-isomers of 3-(2-butylamino)-4H-pyrido[4,3-e]-1,2,4-thiadiazine 1,1-dioxide (BPDZ 42) and 3-(3-methyl-2-butylamino)-4H-pyrido[4,3-e]-1,2,4-thiadiazine 1,1-dioxide (BPDZ 44), two potassium channel openers, is described. Their optical purity was estimated by means of capillary electrophoresis (R- and S-BPDZ 42) and chiral HPLC (R- and S-BPDZ 44). The absolute configuration of each isomer of BPDZ 44 was deduced from crystallographic data. Pharmacological assays performed with the R- and S-isomers of BPDZ 44 revealed only slight differences in their activity on pancreatic B-cells but significant differences in their activity on vascular smooth muscle cells: the R-isomer being sixfold more potent than its corresponding S-isomer. The R-isomer of BPDZ 42 was shown to be more potent than its corresponding S-isomer on the endocrine pancreas. S-BPDZ 44 as well as R- and S-BPDZ 42 were found to exhibit tissue selectivity for the pancreatic versus the vascular smooth muscle tissue.
描述了两种钾通道开放剂3-(2-丁基氨基)-4H-吡啶并[4,3-e]-1,2,4-噻二嗪1,1-二氧化物(BPDZ 42)和3-(3-甲基-2-丁基氨基)-4H-吡啶并[4,3-e]-1,2,4-噻二嗪1,1-二氧化物(BPDZ 44)的R-和S-异构体的制备及其药理学评价。通过毛细管电泳(R-和S-BPDZ 42)和手性高效液相色谱法(R-和S-BPDZ 44)估计它们的光学纯度。BPDZ 44各异构体的绝对构型由晶体学数据推导得出。用BPDZ 44的R-和S-异构体进行的药理学试验显示,它们对胰腺β细胞的活性仅有轻微差异,但对血管平滑肌细胞的活性有显著差异:R-异构体的效力比其相应的S-异构体高六倍。BPDZ 42的R-异构体在内分泌胰腺上比其相应的S-异构体更有效。发现S-BPDZ 44以及R-和S-BPDZ 42对胰腺组织与血管平滑肌组织具有组织选择性。