Liu Yang, Mándi Attila, Li Xiao-Ming, Meng Ling-Hong, Kurtán Tibor, Wang Bin-Gui
Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Nanhai Road 7, Qingdao 266071, China.
University of Chinese Academy of Sciences, Yuquan Road 19A, Beijing 100049, China.
Mar Drugs. 2015 Jun 5;13(6):3640-52. doi: 10.3390/md13063640.
Peniciadametizine A (1); a new dithiodiketopiperazine derivative possessing a unique spiro[furan-2,7'-pyrazino[1,2-b][1,2]oxazine] skeleton, together with a highly oxygenated new analogue, peniciadametizine B (2); as well as two known compounds, brasiliamide A (3); and viridicatumtoxin (4), were isolated and identified from Penicillium adametzioides AS-53, a fungus obtained from an unidentified marine sponge. The unambiguous assignment of the relative and absolute configuration for the spiro center C-2 of compound 1 was solved by the combination of NMR and ECD measurements with Density-Functional Theory (DFT) conformational analysis and Time-Dependent Density-Functional Theory-Electronic Circular Dichroism (TDDFT-ECD) calculations. The spiro[furan-2,7'-pyrazino[1,2-b][1,2]oxazine] skeleton of 1 has not been reported yet among natural products and the biosynthetic pathway for 1 and 2 was discussed. Compounds 1 and 2 showed inhibitory activity against the pathogenic fungus Alternaria brassicae.
青霉地嗪A(1);一种具有独特螺环[呋喃-2,7'-吡嗪并[1,2 - b][1,2]恶嗪]骨架的新型二硫代二酮哌嗪衍生物,以及一种高度氧化的新类似物青霉地嗪B(2);还有两种已知化合物,巴西酰胺A(3)和绿胶霉素(4),是从一种从不明海洋海绵中获得的真菌——亚当齐奥青霉AS - 53中分离并鉴定出来的。通过核磁共振(NMR)和电子圆二色光谱(ECD)测量与密度泛函理论(DFT)构象分析以及含时密度泛函理论 - 电子圆二色光谱(TDDFT - ECD)计算相结合,解决了化合物1中螺环中心C - 2的相对和绝对构型的明确归属问题。1的螺环[呋喃-2,7'-吡嗪并[1,2 - b][1,2]恶嗪]骨架在天然产物中尚未见报道,并且讨论了1和2的生物合成途径。化合物1和2对致病真菌链格孢菌显示出抑制活性。