Caryophyllene sesquiterpenoids with various ring systems from the fungus Pestalotiopsis chamaeropis

Phytochemistry. 2023 Mar:207:113569. doi: 10.1016/j.phytochem.2022.113569. Epub 2022 Dec 22.

Abstract

Six undescribed caryophyllene sesquiterpenoids named pestalotiopsins O-T, along with eight known analogues, were obtained from the fungus Pestalotiopsis chamaeropis. Their structures and absolute configurations were assigned by NMR spectroscopic analyses, HRESIMS, single-crystal X-ray diffraction, electronic circular dichroism (ECD) calculations, Mo2(OAc)4-induced ECD, and chemical derivatization. Pestalotiopsin P represents the first example of a caryophyllene sesquiterpenoid possessing an oxatricyclo [7.2.2.03.6]tridecane decorated with a rare bridgehead double bond, while pestalotiopsin Q has an oxatricyclic [6.3.1.01,4]dodecane skeleton with an unusual ether bridge between C-1 and C-5. These undescribed caryophyllene sesquiterpenoids were screened for their cytotoxic and anti-inflammatory activities.

Keywords: Caryophyllene sesquiterpenoids; Pestalotiopsis chamaeropis; Sporocadaceae.

MeSH terms

  • Fungi
  • Molecular Structure
  • Pestalotiopsis
  • Sesquiterpenes* / chemistry
  • Sesquiterpenes* / pharmacology

Substances

  • caryophyllene
  • Sesquiterpenes

Supplementary concepts

  • Pestalotiopsis chamaeropis