Technology Innovation Center for Exploitation of Marine Biological Resources, Key Laboratory of Marine Genetic Resources, Third Institute of Oceanography, Ministry of Natural Resources, Xiamen 361005, China.
Fangchenggang Center of Inspection and Testing, Fangchenggang 538000, China.
Mar Drugs. 2022 Jun 23;20(7):410. doi: 10.3390/md20070410.
Four novel monocyclic cyclopropane acids, namely, sydocyclopropanes A-D (-), along with one known congener hamavellone B (), were isolated from the MCCC 3A00324 fungus, which was isolated from the deep-sea sediment. The gross structures of novel compounds were established by detailed analyses of the spectroscopic data (HRESIMS and NMR spectra), and their absolute configurations were resolved on the basis of the quantum chemical calculations of ECD and NMR data, in association with DP4+ probability analyses. Sydocyclopropanes A-D, featuring the 1,1,2,3-tetrasubstituted cyclopropane nucleus with different lengthy alkyl side chains, were discovered in nature for the first time. All compounds exhibited antiviral activities against A/WSN/33 (H1N1), with IC values ranging from 26.7 to 77.2 μM, of which compound exhibited a moderate inhibitory effect (IC = 26.7 μM).
从深海沉积物中分离得到的 MCCC 3A00324 真菌中分离得到了 4 种新型单环环丙烷酸,即 sydocyclopropanes A-D(-),以及一种已知的同系物 hamavellone B()。通过详细分析光谱数据(HRESIMS 和 NMR 谱)确定了新化合物的总结构,并基于 ECD 和 NMR 数据的量子化学计算以及 DP4+概率分析确定了它们的绝对构型。Sydocyclopropanes A-D 具有不同长度的烷基侧链的 1,1,2,3-四取代环丙烷核,这在自然界中是首次发现。所有化合物均表现出对 A/WSN/33(H1N1)的抗病毒活性,IC 值范围为 26.7 至 77.2 μM,其中化合物 表现出中等抑制作用(IC = 26.7 μM)。