Avilés Edward, Rodríguez Abimael D
Department of Chemistry, University of Puerto Rico, PO Box 23346, UPR Station, San Juan, PR 00931-3346, United States.
Tetrahedron. 2013 Dec 23;69(51):10797-10804. doi: 10.1016/j.tet.2013.10.095. Epub 2013 Nov 5.
A new investigation of the active sponge extracts of collected off the West coast of Puerto Rico has yielded three new cyclic heptapeptides, namely euryjanicins E ()-G (), containing multiple phenylalanine and proline residues. In CDCl solution, each euryjanicin F () and G () exists as an inseparable complex mixture of conformational isomers. The molecular structures of were elucidated by a combination of chemical degradation, extensive ESI-MS/MS analyses, and 2D NMR methods. The elucidation of the absolute configuration was achieved by HPLC following analysis of the acid hydrolysates after derivatization with Marfey's reagent. When assayed against the National Cancer Institute 60 tumor cell line panel, the new cyclic peptides did not display significant cytotoxicity.
一项对从波多黎各西海岸采集的活性海绵提取物的新研究,得到了三种新的环七肽,即eurynanicins E()-G(),它们含有多个苯丙氨酸和脯氨酸残基。在CDCl溶液中,每种eurynanicin F()和G()都以构象异构体的不可分离的复杂混合物形式存在。通过化学降解、广泛的电喷雾串联质谱(ESI-MS/MS)分析和二维核磁共振(2D NMR)方法相结合,阐明了它们的分子结构。在用Marfey试剂衍生化后的酸水解产物进行分析后,通过高效液相色谱(HPLC)确定了绝对构型。当针对美国国立癌症研究所60种肿瘤细胞系进行检测时,这些新的环肽未显示出显著的细胞毒性。