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Immunosuppressive Cytochalasins from the Mangrove Endophytic Fungus Phomopsis asparagi DHS-48.


ABSTRACT: Three new cytochalasins, phomoparagins A-C (1-3), along with five known analogs (4-8), were isolated from Phomopsis asparagi DHS-48, a mangrove-derived endophytic fungus. Their structures, including their absolute configurations, were elucidated using a combination of detailed HRESIMS, NMR, and ECD techniques. Notably, 1 possessed an unprecedented 5/6/5/8/5-fused pentacyclic skeleton. These compounds were tested for their inhibitory activity against concanavalin A (ConA)/lipopolysaccharide (LPS)-induced spleen lymphocyte proliferation and calcineurin (CN) enzyme. Several metabolites (2 and 4-6) exhibited fascinating inhibitory activities with a relatively low toxicity. Furthermore, 2 was demonstrated to inhibit ConA-stimulated activation of NFAT1 dephosphorylation and block NFAT1 translocation in vitro, subsequently inhibiting the transcription of interleukin-2 (IL-2). Our results provide evidence that 2 may, at least partially, suppress the activation of spleen lymphocytes via the CN/NFAT signaling pathway, highlighting that it could serve as an effective immunosuppressant that is noncytotoxic and natural.

SUBMITTER: Feng Z 

PROVIDER: S-EPMC9409992 | biostudies-literature | 2022 Aug

REPOSITORIES: biostudies-literature

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Immunosuppressive Cytochalasins from the Mangrove Endophytic Fungus <i>Phomopsis asparagi</i> DHS-48.

Feng Zhao Z   Zhang Xuexia X   Wu Jingwan J   Wei Chengwen C   Feng Ting T   Zhou Dongdong D   Wen Zhenchang Z   Xu Jing J  

Marine drugs 20220818 8


Three new cytochalasins, phomoparagins A-C (<b>1</b>-<b>3</b>), along with five known analogs (<b>4</b>-<b>8</b>), were isolated from <i>Phomopsis asparagi</i> DHS-48, a mangrove-derived endophytic fungus. Their structures, including their absolute configurations, were elucidated using a combination of detailed HRESIMS, NMR, and ECD techniques. Notably, <b>1</b> possessed an unprecedented 5/6/5/8/5-fused pentacyclic skeleton. These compounds were tested for their inhibitory activity against conc  ...[more]

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