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阿普拉毒素E,一种从关岛采集的海洋蓝藻布氏鞘丝藻中提取的具有细胞毒性的缩肽内酯。

Apratoxin E, a cytotoxic peptolide from a guamanian collection of the marine cyanobacterium Lyngbya bouillonii.

作者信息

Matthew Susan, Schupp Peter J, Luesch Hendrik

机构信息

Department of Medicinal Chemistry, University of Florida, 1600 SW Archer Road, GainesVille, Florida 32610, USA.

出版信息

J Nat Prod. 2008 Jun;71(6):1113-6. doi: 10.1021/np700717s. Epub 2008 May 8.

Abstract

A collection of the marine cyanobacterium Lyngbya bouillonii from Guam afforded apratoxin E (1), a new peptide-polyketide hybrid of the apratoxin class of cytotoxins. The planar structure of 1 was elucidated by NMR spectroscopic analysis and mass spectrometry. Configurational assignments of stereocenters in the peptide portion were made by chiral HPLC analysis of the acid hydrolysate. The relative configuration in the polyketide moiety was assigned by comparison of NMR data including proton-proton coupling constants with those of the known analogues. Apratoxin E (1) displayed strong cytotoxicity against several cancer cell lines derived from colon, cervix, and bone, ranging from 21 to 72 nM, suggesting that the alpha,beta-unsaturation of the modified cysteine residue is not essential for apratoxin activity. The 5- to 15-fold reduced activity compared with apratoxin A (2) is attributed to the dehydration in the long-chain polyketide unit, which could affect the conformation of the molecule.

摘要

从关岛采集的海洋蓝藻布氏鞘丝藻中分离得到了阿普拉毒素E(1),它是一种新型的细胞毒素类阿普拉毒素肽 - 聚酮杂合物。通过核磁共振光谱分析和质谱法阐明了1的平面结构。肽部分手性中心的构型归属通过酸水解产物的手性高效液相色谱分析确定。通过将包括质子 - 质子耦合常数在内的核磁共振数据与已知类似物的数据进行比较,确定了聚酮部分的相对构型。阿普拉毒素E(1)对几种源自结肠、宫颈和骨骼的癌细胞系显示出强烈的细胞毒性,范围为21至72 nM,这表明修饰的半胱氨酸残基的α,β - 不饱和对于阿普拉毒素活性并非必不可少。与阿普拉毒素A(2)相比,活性降低了5至15倍归因于长链聚酮单元中的脱水,这可能会影响分子的构象。

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