Discovery of Neuritogenic Securinega Alkaloids from Flueggea suffruticosa by a Building Blocks‐Based Molecular Network Strategy. (28th July 2021)

• Record Type: Journal Article
• Authors: He, Qi‐Fang; Wu, Zhen‐Long; Li, Liuren; Sun, Wan‐Yang; Wang, Gui‐Yang; Jiang, Ren‐Wang; Hu, Li‐Jun; Shi, Lei; He, Rong‐Rong; Wang, Ying; Ye, Wen‐Cai
• Is Part Of: Angewandte Chemie. Volume 133:Number 36(2021)
• Page Start: 19761
• Page End: 19765
• Publication Date: 2021-07-28
• Subjects: alkaloids -- building blocks-based molecular network -- natural products -- neuronal differentiation -- structure elucidation; Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.202103878
• Languages: English
• ISSNs: 0044-8249

Abstract

Abstract: A combined strategy of building blocks recognition and molecular network construction, termed the building blocks‐based molecular network (BBMN), was first presented to facilitate the efficient discovery of novel natural products. By mapping the BBMN of the total alkaloid fraction of Flueggea suffruticosa, three Securinega alkaloids (SEAs) with unusual chemical architectures, suffranidines A–C (1 –3 ), were discovered and isolated. Compound 1 characterizes an unprecedented 8/5/6/5/6/6/6/6‐fused octacyclic scaffold with a unique cage‐shaped 3‐azatricyclo[6.4.0.0 3, 11 ]dodecane core. Compounds 2 and 3 are highly modified SEA dimers that incorporate additional C6 motifs. A hypothetical biosynthetic pathway for 1 –3 was proposed. In addition, 1 significantly induced neuronal differentiation and neurite extension by upregulating eukaryotic elongation factor 2 (eEF2)‐mediated protein synthesis. Abstract : A building blocks‐based molecular network (BBMN) strategy was first presented and resulted in the discovery of three novel Securinega alkaloids. Compound 1 features an unprecedented 8/5/6/5/6/6/6/6‐fused octacyclic scaffold with a unique cage‐shaped 3‐azatricyclo[6.4.0.0 3, 11 ]dodecane core, which also exhibited remarkable effects on neuronal differentiation and neurite extension.