Department of Pharmacy, Section for Pharmaceutical Chemistry, University of Oslo, P.O. Box 1068, 0316 Oslo, Norway.
J Nat Prod. 2020 Jul 24;83(7):2255-2260. doi: 10.1021/acs.jnatprod.0c00385. Epub 2020 Jun 16.
The resolution of inflammation is governed by the active biosynthesis of specialized pro-resolving mediators using ω-6 and ω-3 polyunsaturated fatty acids as substrates. These mediators act as resolution agonists and display several interesting bioactivities. PD2 is an oxygenated polyunsaturated fatty acid biosynthesized from n-3 docosapentaenoic acid belonging to the specialized pro-resolving lipid mediator family named protectins. The protectins exhibit anti-inflammatory properties and pro-resolving bioactivities. These endogenously produced compounds are of interest as leads in resolution pharmacology and drug development. Herein, together with its NMR, MS, and UV data, a stereoselective total synthesis of PD2 is presented.
炎症的消退是由专门的促解决介质的主动生物合成控制的,这些介质使用 ω-6 和 ω-3 多不饱和脂肪酸作为底物。这些介质作为解决激动剂发挥作用,并表现出几种有趣的生物活性。PD2 是一种从属于被称为保护素的专门促解决脂质介质家族的 n-3 二十二碳五烯酸生物合成的含氧多不饱和脂肪酸。保护素有抗炎和促解决的生物活性。这些内源性化合物作为解决药理学和药物开发的先导化合物很有意义。本文结合其 NMR、MS 和 UV 数据,展示了 PD2 的立体选择性全合成。