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比卡酰胺 A-D,一种来源于海洋海绵的独特聚酮化合物,作为适应营养饥饿的肿瘤细胞的选择性生长抑制剂。

Biakamides A-D, Unique Polyketides from a Marine Sponge, Act as Selective Growth Inhibitors of Tumor Cells Adapted to Nutrient Starvation.

机构信息

Graduate School of Pharmaceutical Sciences, Osaka University , Yamada-oka 1-6, Suita, Osaka 565-0871, Japan.

Department of Chemistry, Faculty of Science, Lampung University , Jl. Prof. Dr. Sumantri Brodjonegoro No. 1, Bandar, Lampung 35145, Indonesia.

出版信息

J Org Chem. 2017 Feb 3;82(3):1705-1718. doi: 10.1021/acs.joc.6b02948. Epub 2017 Jan 25.

Abstract

Biakamides A-D, novel unusually unique polyketides, were isolated from an Indonesian marine sponge (Petrosaspongia sp.) with a constructed bioassay using PANC-1 human pancreatic cancer cells. Through detailed analyses of the one- and two-dimensional NMR spectra of biakamides, planar chemical structures possessing a terminal thiazole, two N-methyl amides, a chloromethylene, and a substituted butyryl moiety were obtained. After elucidation of the configuration of the secondary alcohol moiety in biakamides A and B, the absolute stereostructures of the two secondary methyl groups in biakamides A-D were determined by the asymmetric total syntheses of all possible stereoisomers from the optically pure monoprotected 2,4-dimethyl-1,5-diol. Biakamides A-D showed selective antiproliferative activities against PANC-1 cells cultured under glucose-deficient conditions in a concentration-dependent manner. The primary mode of action of biakamides was found to be inhibition of complex I in the mitochondrial electron transport chain.

摘要

比卡酰胺 A-D,新型独特的聚酮类化合物,从印度尼西亚海绵(Petrosaspongia sp.)中分离出来,该海绵通过使用 PANC-1 人胰腺癌细胞构建的生物测定法进行分离。通过对比卡酰胺的一维和二维 NMR 光谱的详细分析,得到了具有末端噻唑、两个 N-甲基酰胺、氯亚甲基和取代丁酰部分的平面化学结构。在阐明比卡酰胺 A 和 B 中仲醇部分的构型后,通过从光学纯单保护 2,4-二甲基-1,5-二醇中对所有可能的立体异构体进行不对称全合成,确定了比卡酰胺 A-D 中两个仲甲基的绝对立体结构。比卡酰胺 A-D 对葡萄糖缺乏条件下培养的 PANC-1 细胞表现出选择性的抗增殖活性,呈浓度依赖性。比卡酰胺的主要作用模式被发现是抑制线粒体电子传递链中的复合物 I。

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