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Synthesis of N-Boc Protected Hydrazine Diacids as Key Structural Units for the Formation of α-Helix Mimics

机译:N-BOC保护的肼二酸的合成作为形成α-Helix模拟的关键结构单元

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Many diseases, such as autoimmunity, cancer, inflammatory, and neurodegenerative disorders are the result of disregulation of the apoptotic process. Within the B-cell lymphoma-2 (Bcl-2) family, the overall interaction of anti and pro-apoptotic proteins play a major role in regulating apoptosis. Several studies have demonstrated that overexpression of anti-apoptotic Bcl-2 and Bcl-x_L proteins is associated with tumor progression and drug resistance [1]. Previously reported peptidomimetics that inhibit the interaction between pro-apoptotic BH3 domains and Bcl-2 family proteins contain hydrophobic scaffolds that would diminish their use as potential drugs [2]. We report the synthesis of key monomer building blocks for the formation of more hydrophilic compounds based on hydrazine linked piperazine-2,6-dione scaffolds (Figure 1).
机译:许多疾病,如自身免疫,癌症,炎症和神经退行性障碍是对凋亡过程的负担的结果。在B细胞淋巴瘤-2(BCL-2)家族中,抗凋亡蛋白的整体相互作用在调节细胞凋亡中起主要作用。几项研究表明,抗凋亡Bcl-2和Bcl-X1蛋白的过度表达与肿瘤进展和耐药相关[1]。先前报道抑制促凋亡BH3结构域和Bcl-2家族蛋白质之间的相互作用的肽菌药含有疏水性支架,其将其作为潜在药物的用途递减[2]。我们报道了基于肼连接的哌嗪-2,6-二酮支架形成更多亲水化合物的关键单体构建块的合成(图1)。

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