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Two New Picoline-Derived Meroterpenoids with Anti-Acetylcholinesterase Activity from Ascidian-Derived Fungus Amphichorda felina.


ABSTRACT: Amphichoterpenoids D (1) and E (2), two new picoline-derived meroterpenoids with a rare 6/6/6 tricyclic pyrano[3,2-c]pyridinyl-γ-pyranone scaffold, were isolated from the ascidian-derived fungus Amphichorda felina SYSU-MS7908. Their structures, including the absolute configurations, were established by extensive spectroscopic methods (1D and 2D NMR and high-resolution mass spectrometry) and ECD calculations. Compounds 1 and 2 showed anti-acetylcholinesterase (anti-AChE) activities with IC50 values of 12.5 μM and 11.6 μM, respectively. The binding interactions between 1, 2, and AChE were investigated using molecular docking analyses.

SUBMITTER: Jiang M 

PROVIDER: S-EPMC9416303 | biostudies-literature | 2022 Aug

REPOSITORIES: biostudies-literature

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Two New Picoline-Derived Meroterpenoids with Anti-Acetylcholinesterase Activity from Ascidian-Derived Fungus <i>Amphichorda felina</i>.

Jiang Minghua M   Guo Heng H   Wu Qilin Q   Yuan Siwen S   Liu Lan L  

Molecules (Basel, Switzerland) 20220810 16


Amphichoterpenoids D (<b>1</b>) and E (<b>2</b>), two new picoline-derived meroterpenoids with a rare 6/6/6 tricyclic pyrano[3,2-c]pyridinyl-<i>γ</i>-pyranone scaffold, were isolated from the ascidian-derived fungus <i>Amphichorda felina</i> SYSU-MS7908. Their structures, including the absolute configurations, were established by extensive spectroscopic methods (1D and 2D NMR and high-resolution mass spectrometry) and ECD calculations. Compounds <b>1</b> and <b>2</b> showed anti-acetylcholineste  ...[more]

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