The pyridino prostanoids 9, 12 and 14 have been synthesized (in racemic form) and have been found to be effective inhibitors of the biosynthesis of thromboxane A2 in human platelets (IC50 1–3 μM).
吡啶类
前列腺素9、12和14已被合成(外消旋形式),并被发现是人类血小板中血栓烷A 2
生物合成的有效
抑制剂(IC 50 1-3μM)。