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Multicomponent synthesis of dihydrobenzoxazepinones, bearing four diversity points, as potential α-helix mimics

机译:多组分合成具有四个多样性点的二氢苯并恶嗪酮类化合物,作为潜在的α-螺旋模拟物

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摘要

A very short convergent synthesis of dihydrobenzoxazepinones, bearing four diverse diversity points, based on coupling the Ugi reaction with a Mitsunobu cyclization, was developed. These compounds are potential α-helix mimics, where three of the four appendages are expected to imitate the residues in i, i + 4 and i + 7 positions. A library of 22 compounds bearing lipophilic substituents, designed to interact with the hydrophobic cleft of anti-apoptotic protein Bcl-xL, was synthesized. Preliminary biochemical tests, based on competitive binding, have already been carried out.
机译:基于Ugi反应与Mitsunobu环化的偶联,开发了具有四个不同多样性点的非常短的会聚二氢苯并恶嗪酮的合成方法。这些化合物是潜在的α-螺旋模拟物,预计四个附件中的三个将模仿i,i + 4和i + 7位置的残基。合成了22个带有亲脂性取代基的化合物的库,该库设计用于与抗凋亡蛋白Bcl-xL的疏水性缝隙相互作用。基于竞争结合的初步生化测试已经进行。

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