Targeted isolation of two disesquiterpenoid macrocephadiolides A and B from Ainsliaea macrocephala using a molecular networking-based dereplication strategy. Issue 12 (18th May 2020)

• Record Type: Journal Article
• Authors: Ren, Yong-Mei; Zhou, Shuai-Zhen; Zhang, Tian; Qian, Meijia; Zhang, Rui; Yao, Sheng; Zhu, Hong; Tang, Chunping; Lin, Ligen; Ye, Yang
• Is Part Of: Organic chemistry frontiers. Volume 7:Issue 12(2020)
• Page Start: 1481
• Page End: 1489
• Publication Date: 2020-05-18
• Subjects: Chemistry, Organic -- Periodicals; 547.005
• DOI: 10.1039/d0qo00030b
• Languages: English
• ISSNs: 2052-4110

Abstract

Abstract : Two novel dimeric sesquiterpenoids with potent anti-inflammatory activity were characterized from Ainsliaea macrocephala through a molecular networking-based dereplication strategy. Abstract : A molecular networking-based dereplication strategy was applied for the phytochemical investigation of Ainsliaea macrocephala, leading to the isolation of two novel disesquiterpenoid macrocephadiolides A (1 ) and B (2 ). Their structures, featuring a rare 5, 6-spirocyclic ketal lactone core and a C-15/C-15′ linkage between a guaianolide and a 3, 4- seco -guaianolide monomer, respectively, were established by extensive spectroscopic analysis and confirmed further by single-crystal X-ray crystallography. Compounds 1 and 2 showed a potent inhibitory effect on nitric oxide (NO) production, with IC50 values of 0.99 and 6.13 μM, respectively, in lipopolysaccharide (LPS)-stimulated RAW264.7 macrophages. Compound 1 dose-dependently suppressed the expression of inducible NO oxidase (iNOS) through inhibiting nuclear factor-κB (NF-κB) activation.