Yamaguchi M, Maruyama N, Koga T, Kamei K, Akima M, Kuroki T, Hamana M, Ohi N
Fuji-gotemba Research Laboratories, Chugai Pharmaceutical Company, Ltd. Shizuoka, Japan.
Chem Pharm Bull (Tokyo). 1995 Feb;43(2):332-4. doi: 10.1248/cpb.43.332.
Synthesis and pharmacological evaluation of novel indazole derivatives are described. These compounds were found to exhibit both thromboxane A2 (TXA2) synthetase-inhibitory and bronchodilatory activities. This observation supports the idea that the partial structure of the 3-pyridyl and phenyl groups with a methylene insertion is an important component for well-balanced activities.
描述了新型吲唑衍生物的合成及药理评价。发现这些化合物具有血栓素A2(TXA2)合成酶抑制活性和支气管扩张活性。这一观察结果支持了这样一种观点,即带有亚甲基插入的3-吡啶基和苯基的部分结构是实现平衡活性的重要组成部分。