Xiamen Key Laboratory of Marine Medicinal Natural Product Resources, Xiamen Medical College, Xiamen, 361023, P. R. China.
Engineering Research Center of Marine Biopharmaceutical Resource, Fujian Province University, Xiamen Medical College, Xiamen, 361023, P. R. China.
Chem Biodivers. 2022 Jul;19(7):e202200311. doi: 10.1002/cbdv.202200311. Epub 2022 Jun 8.
Chemical investigation of the EtOH extract of the sponge Axinella sp. collected from the South China Sea resulted in the identification of one new pyrrololactam alkaloid, axinellamine E (2), along with four known analogs (1, 3-5). Compound 1 was initially separated as enantiomers and was further separated to be optically pure compounds (1 a and 1 b) by a chiral column. The planar structure of compound 2 was determined mainly by 1D-, 2D-NMR, and HR-ESI-MS data analyses. Absolute configurations of 1 a and 1 b was defined by calculated ECD spectra method. All of the compounds were evaluated for their anti-inflammatory activities against nitric oxide production in lipopolysaccharide-induced RAW 264.7 cells among which compound 1 showed weak activity at 40 μg/mL. Plausible biosynthetic pathways corresponding to aldisine analogs of 1, 2, 4, and 5 were also discussed.
从南海采集的海绵 Axinella sp 的 EtOH 提取物的化学研究鉴定出一种新的吡咯烷酮生物碱,即 axinellamine E(2),以及四个已知类似物(1、3-5)。化合物 1 最初被分离为对映异构体,并通过手性柱进一步分离为光学纯化合物(1a 和 1b)。化合物 2 的平面结构主要通过 1D、2D-NMR 和 HR-ESI-MS 数据分析确定。通过计算 ECD 光谱方法确定了 1a 和 1b 的绝对构型。所有化合物均针对其在脂多糖诱导的 RAW 264.7 细胞中产生一氧化氮的抗炎活性进行了评估,其中化合物 1 在 40 μg/mL 时表现出较弱的活性。还讨论了与 1、2、4 和 5 的 aldisine 类似物相对应的可能生物合成途径。