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Synthesis of neolamellarin A, an inhibitor of hypoxia-inducible factor-1

机译:缺氧诱导因子1抑制剂新薄层蛋白A的合成

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摘要

Neolamellarin A, a metabolite isolated from the sponge Dendrilla nigra, was found to inhibit hypoxia-inducible factor-1 (HIF-1) activation by 26% at 10 μ M concentration and inhibition of HIF-1 has become a major antitumor molecular target. Herein the first synthesis of neolamellarin A is described. The synthetic strategy features the condensation of vinylogous amide with aminomalonate to construct the 3,4-bis(4-methoxyphenyl)-1H-pyrrole core and the subsequent acylation and deprotection rendered the target compound in 18% over all yield.
机译:新海绵蛋白A是从海绵黑头粉刺中分离出的代谢产物,被发现在10μM的浓度下可抑制26%的缺氧诱导因子1(HIF-1)活化,抑制HIF-1已成为主要的抗肿瘤分子靶标。在此描述了新层蛋白A的第一合成。合成策略的特征是乙烯基酰胺与氨基丙二酸的缩合反应以构建3,4-双(4-甲氧基苯基)-1H-吡咯核,随后的酰化和脱保护作用使目标化合物的收率为18%。

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