Soldatov N M
Biokhimiia. 1988 Jul;53(7):1059-68.
The synthesis and biological activity of some novel analogs of the calcium channel blocker nifedipine, i.e., derivatives of 2.6-dimethyl-3.5-diethoxycarbonyl-4-(3-nitrophenyl)-1.4-dihydropyridine (DHP) were studied. One radioactive and two photoactivable DHP derivatives were obtained. DHP hemisuccinate was used to prepare an affinity matrix, DHP-Sepharose as well as a DHP-albumin conjugate; the latter was used for anti-DHP antibodies generation in rabbits. All novel DHP derivatives were obtained from a single key 3-hydroxycarbonyl DHP derivative, and they comprise a series of necessary tools for the study and isolation of membrane calcium channels.
研究了钙通道阻滞剂硝苯地平的一些新型类似物,即2,6 - 二甲基 - 3,5 - 二乙氧羰基 - 4 - (3 - 硝基苯基) - 1,4 - 二氢吡啶(DHP)的衍生物的合成及其生物活性。得到了一种放射性和两种光活化的DHP衍生物。DHP半琥珀酸酯用于制备亲和基质DHP - 琼脂糖以及DHP - 白蛋白偶联物;后者用于在兔体内产生抗DHP抗体。所有新型DHP衍生物均由单一关键的3 - 羟基羰基DHP衍生物制得,它们构成了用于研究和分离膜钙通道的一系列必要工具。