Molecules (Mar 2024)

Di-Isatropolone C, a Spontaneous Isatropolone C Dimer Derivative with Autophagy Activity

  • Jie Fu,
  • Xiaoyan Liu,
  • Miaoqing Zhang,
  • Jiachang Liu,
  • Shufen Li,
  • Bingya Jiang,
  • Linzhuan Wu

DOI
https://doi.org/10.3390/molecules29071477
Journal volume & issue
Vol. 29, no. 7
p. 1477

Abstract

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Isatropolone C from Streptomyces sp. CPCC 204095 features a fused cyclopentadienone-tropolone-oxacyclohexadiene tricyclic moiety in its structure. Herein, we report an isatropolone C dimer derivative, di-isatropolone C, formed spontaneously from isatropolone C in methanol. Notably, the structure of di-isatropolone C resolved by NMR reveals a newly formed cyclopentane ring to associate the two isatropolone C monomers. The configurations of four chiral carbons, including a ketal one, in the cyclopentane ring are assigned using quantum NMR calculations and DP4+ probability. The plausible molecular mechanism for di-isatropolone C formation is proposed, in which complex dehydrogenative C-C bond coupling may have happened to connect the two isatropolone C monomers. Like isatropolone C, di-isatropolone C shows the biological activity of inducing autophagy in HepG2 cells.

Keywords