Chen Xiao-Dan, Li Xin, Li Xiao-Ming, Yang Sui-Qun, Wang Bin-Gui
CAS and Shandong Province 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. 2024 Dec 22;22(12):574. doi: 10.3390/md22120574.
Six new sesquiterpenes, including four eremophilane derivatives fureremophilanes A-D (-) and two acorane analogues furacoranes A and B ( and ), were characterized from the culture extract of the cold-seep derived fungus CS-280 co-cultured with autoclaved QDIO-4. All the six compounds were highly oxygenated especially and with infrequent epoxyethane and tetrahydrofuran ring systems. The structures of - were established on the basis of detailed interpretation of 1D and 2D NMR and MS data. Their relative and absolute configurations were assigned by a combination of NOESY and single crystal X-ray crystallographic analysis, and by time-dependent density functional (TDDFT) ECD calculations as well. All compounds were tested the anti-inflammatory activity against human COX-2 protein, among which, compounds and displayed activities with IC values 123.00 µM and 93.45 µM, respectively. The interaction mechanism was interpreted by molecular docking.
从与高压灭菌的QDIO-4共培养的冷泉来源真菌CS-280的培养提取物中鉴定出六种新的倍半萜,包括四种艾里莫芬烷衍生物呋喃艾里莫芬烷A-D(-)和两种菖蒲烷类似物呋喃菖蒲烷A和B(和)。所有六种化合物都具有高度氧化的特点,尤其是呋喃艾里莫芬烷A和B具有罕见的环氧乙烷和四氢呋喃环系统。呋喃艾里莫芬烷A-D的结构是在对一维和二维核磁共振以及质谱数据进行详细解析的基础上确定的。它们的相对构型和绝对构型通过核Overhauser效应光谱(NOESY)和单晶X射线晶体学分析相结合的方法确定,同时也通过含时密度泛函(TDDFT)电子圆二色(ECD)计算确定。所有化合物都针对人环氧化酶-2(COX-2)蛋白进行了抗炎活性测试,其中,呋喃艾里莫芬烷A和B分别以123.00 μM和93.45 μM的半数抑制浓度(IC)显示出活性。通过分子对接解释了其相互作用机制。