Tong Y, Fobian Y M, Wu M, Boyd N D, Moeller K D
Department of Chemistry, Washington University, St. Louis, MO 63130, USA.
Bioorg Med Chem Lett. 1998 Jul 7;8(13):1679-82. doi: 10.1016/s0960-894x(98)00289-3.
Three substance P analogs with conformation constraints in the Phe7-Phe8 region have been prepared in connection with an effort to differentiate two families of potential conformations for the binding of substance P to its NK1 receptor. While the analogs did not bind the NK1 receptor with high affinity, the synthesis of the analogs demonstrated the utility of a general method for constructing piperazinone based peptidomimetics.
为了区分P物质与其NK1受体结合的两个潜在构象家族,人们制备了三种在Phe7 - Phe8区域具有构象限制的P物质类似物。虽然这些类似物并未以高亲和力结合NK1受体,但类似物的合成证明了一种构建基于哌嗪酮的拟肽的通用方法的实用性。