Phytochemistry2022,Vol.19411.DOI:10.1016/j.phytochem.2021.113006

Jellynolide A, pokepola esters, and sponalisolides from the aquaculture sponge Spongia officinalis L

Jin, Tianyun Li, Pinglin Wang, Cili Tang, Xuli Yu, Xiaoli Sun, Fengqing Luo, Lianzhong Ou, Huilong Li, Guoqiang
Phytochemistry2022,Vol.19411.DOI:10.1016/j.phytochem.2021.113006

Jellynolide A, pokepola esters, and sponalisolides from the aquaculture sponge Spongia officinalis L

Jin, Tianyun 1Li, Pinglin 1Wang, Cili 1Tang, Xuli 1Yu, Xiaoli 1Sun, Fengqing 1Luo, Lianzhong 2Ou, Huilong 3Li, Guoqiang1
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作者信息

  • 1. Ocean Univ China
  • 2. Xiamen Med Coll
  • 3. Hainan Univ
  • 折叠

Abstract

Jellynolide A, an unreported bicyclic diterpenoid with an unprecedented penta-substituted carbon skeleton which implied an irregular biogenic pathway, together with four pairs of rare phosphate triesters, (+/-)-pokepola ester B-E, one undescribed related racemic furanoterpenoid, (+/-)-sponalisolide C, one undescribed furanoterpenoid, (-)-sponalisolide D, and two known (+/-)-sponalisolide B and dendrolasin carboxylic acid were isolated from the aquaculture Spongia officinalis L. Their structures were elucidated by comprehensive spectroscopic analysis, quantum chemical calculation of NMR parameters, and electronic circular dichroism (ECD). The plausible biosynthetic pathway of jellynolide A was proposed. (+/-)-Pokepola ester C exhibited significant inhibition against Wnt, HIF1 signaling pathways. (+)-Pokepola ester B and (-)-pokepola ester D showed moderate cytotoxicity activities.

Key words

Spongia officinalis L./Spongidae/Aquaculture sponge/Terpenoids/Phosphate triester/Biological activity/MARINE SPONGE/DERIVATIVES/INHIBITORS/DITERPENE/BIOSYNTHESIS/COMPUTATION/DISCOVERY/PATHWAY

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出版年

2022
Phytochemistry

Phytochemistry

CCR
ISSN:0031-9422
被引量2
参考文献量51
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