Axinellamine E, One New Pyrrololactam Alkaloid from the South China Sea Sponge Axinella sp.
Li XuPanpan WangShijie YuanLiangzhou YuJianping ZhaoGuoqiang LiGang ZhangLianzhong LuoPublished in: Chemistry & biodiversity (2022)
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.
Keyphrases
- lipopolysaccharide induced
- anti inflammatory
- nitric oxide
- ms ms
- inflammatory response
- induced apoptosis
- molecular docking
- mass spectrometry
- multiple sclerosis
- capillary electrophoresis
- magnetic resonance
- cell cycle arrest
- oxidative stress
- electronic health record
- high resolution
- liquid chromatography
- cell death
- ionic liquid
- machine learning
- bioinformatics analysis
- cell proliferation
- solid state