Issue 12, 2024

(±)-Hypandrone A, a pair of polycyclic polyprenylated acylphloroglucinol enantiomers with a caged 7/6/5/6/6 pentacyclic skeleton from Hypericum androsaemum

Abstract

(±)-Hypandrone A (1), a pair of highly modified polycyclic polyprenylated acylphloroglucinol (PPAP) enantiomers, with an unprecedented caged 2,8,17-trioxapentacyclo-[11.4.2.01,9.04,9.010,15]-nonadecane core, were isolated from the fruits of Hypericum androsaemum. The racemate (±)-1 was successfully separated into the two optically pure enantiomers (ee ≥ 99%) using a preparative HPLC system. Their structures including absolute configurations were elucidated via spectroscopic analyses, electronic circular dichroism calculations, and single-crystal X-ray diffraction. Biological studies revealed that (−)-1 is a potent inhibitor of the NLRP3 inflammasome pathway and could inhibit the protein expression of NLRP3, ASC, cleaved caspase-1 and the active form N-GSDMD fragment, thereby blocking NLRP3 inflammasome-induced pyroptosis.

Graphical abstract: (±)-Hypandrone A, a pair of polycyclic polyprenylated acylphloroglucinol enantiomers with a caged 7/6/5/6/6 pentacyclic skeleton from Hypericum androsaemum

Supplementary files

Article information

Article type
Research Article
Submitted
09 Mar 2024
Accepted
27 Apr 2024
First published
03 May 2024

Org. Chem. Front., 2024,11, 3459-3464

(±)-Hypandrone A, a pair of polycyclic polyprenylated acylphloroglucinol enantiomers with a caged 7/6/5/6/6 pentacyclic skeleton from Hypericum androsaemum

J. Wei, P. Fan, Y. Huang, H. Zeng, R. Jiang, Z. Wu, Y. Zhang and Z. Hu, Org. Chem. Front., 2024, 11, 3459 DOI: 10.1039/D4QO00444B

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