Hedner Erik, Sjögren Martin, Hodzic Said, Andersson Rolf, Göransson Ulf, Jonsson Per R, Bohlin Lars
Department of Medicinal Chemistry, Uppsala University , Sweden.
J Nat Prod. 2008 Mar;71(3):330-3. doi: 10.1021/np0705209. Epub 2008 Feb 14.
Many sessile suspension-feeding marine organisms rely on chemical defense to keep their surfaces free from fouling organisms. The brominated cyclopeptides barettin (cyclo[(6-bromo-8-entryptophan)arginine]) ( 1) and 8,9-dihydrobarettin (cyclo[(6-bromotryptophan)arginine]) ( 2) from the cold-water sponge Geodia barretti have previously displayed settlement inhibition of barnacle larvae in a dose-dependent manner. In this paper, we describe a novel dibrominated cyclopeptide, bromobenzisoxazolone barettin (cyclo[(6-bromo-8-(6-bromobenzioxazol-3(1 H)-one)-8-hydroxy)tryptophan)]arginine) ( 3), which we have isolated from G. barretti and which displays settlement inhibition of barnacle larvae ( Balanus improvisus) with an EC 50 value of 15 nM. The chemical structure was determined using MS and 2D-NMR.
许多固着型悬浮取食海洋生物依靠化学防御来保持其表面无污损生物。来自冷水海绵巴氏吉奥海绵(Geodia barretti)的溴化环肽巴雷廷(环[(6-溴-8-表色氨酸)精氨酸])(1)和8,9-二氢巴雷廷(环[(6-溴色氨酸)精氨酸])(2)先前已显示出对藤壶幼虫的附着抑制作用,且呈剂量依赖性。在本文中,我们描述了一种新型二溴化环肽,溴苯并异恶唑酮巴雷廷(环[(6-溴-8-(6-溴苯并异恶唑-3(1H)-酮)-8-羟基)色氨酸]精氨酸)(3),我们已从巴氏吉奥海绵中分离出该物质,它对藤壶幼虫(Balanus improvisus)的附着具有抑制作用,其半数有效浓度(EC50)值为15 nM。使用质谱(MS)和二维核磁共振(2D-NMR)确定了其化学结构。