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来自巴拿马海洋蓝藻 Lyngbya majuscula 的生物活性对称环二肽 malyngolide 二聚体。

Malyngolide dimer, a bioactive symmetric cyclodepside from the panamanian marine cyanobacterium Lyngbya majuscula.

机构信息

Center for Marine Biotechnology and Biomedicine, Scripps Institution of Oceanography and Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, La Jolla, California 92093, USA.

出版信息

J Nat Prod. 2010 Apr 23;73(4):709-11. doi: 10.1021/np9005184.

Abstract

Fractionation of the extract of the marine cyanobacterium Lyngbya majuscula collected from Panama led to the isolation of malyngolide dimer (1). The planar structure of 1 was determined using 1D and 2D NMR spectroscopy and HRESI-TOFMS. The absolute configuration was established by chemical degradation followed by chiral GC-MS analyses and comparisons with an authentic sample of malyngolide seco-acid (4). Compound 1 showed moderate in vitro antimalarial activity against chloroquine-resistant Plasmodium falciparum (W2) (IC(50) = 19 microM) but roughly equivalent toxicity against H-460 human lung cell lines. Furthermore, because the closely related cyanobacterial natural product tanikolide dimer (5) was a potent SIRT2 inhibitor, compound 1 was evaluated in this assay but found to be essentially inactive.

摘要

从巴拿马采集的海洋蓝藻 Lyngbya majuscula 的提取物进行分段提取,得到了马缨丹内酯二聚体(1)。通过 1D 和 2D NMR 光谱和 HRESI-TOFMS 确定了 1 的平面结构。通过化学降解,然后进行手性 GC-MS 分析,并与马缨丹内酯 seco-acid(4)的真实样品进行比较,确定了其绝对构型。化合物 1 对氯喹耐药的恶性疟原虫(W2)(IC(50)= 19 μM)表现出中等的体外抗疟活性,但对 H-460 人肺细胞系的毒性大致相当。此外,由于密切相关的蓝藻天然产物 tanikolide 二聚体(5)是一种有效的 SIRT2 抑制剂,因此对化合物 1 进行了该测定,但发现其基本上无活性。

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