become a popular drug target due to its harmful physiological roles. Diarylheptanoids are one class of compounds that have shown successful inhibition of PGE2. This paper reports the synthesis and PGE2 inhibitory activity of a series of analogues of a naturally occurring diarylheptanoid. The most efficacious compounds were examined for dose-dependent PGE2 inhibition. Among several promising compounds
前列腺素E 2(
PGE 2)是炎症的脂质介质,由于其有害的生理作用,其抑制作用已成为流行的药物靶标。二芳基
庚烷类化合物是已显示出成功抑制
PGE 2的一类化合物。本文报道了一系列天然存在的二芳基
庚烷类似物的合成和
PGE 2抑制活性。检查了最有效的化合物对剂量依赖性
PGE 2的抑制作用。在几种有前途的化合物中,潜在候选化合物的IC 50值为0.56 ng / µL或1.7 µM,在最高剂量为10 ng / µL时没有可检测到的毒性。