Eremophilane- and Acorane-Type Sesquiterpenes from the Deep-Sea Cold-Seep-Derived Fungus Furcasterigmium furcatum CS-280 Cultured in the Presence of Autoclaved Pseudomonas aeruginosa QDIO-4

Mar Drugs. 2024 Dec 22;22(12):574. doi: 10.3390/md22120574.

Abstract

Six new sesquiterpenes, including four eremophilane derivatives fureremophilanes A-D (1-4) and two acorane analogues furacoranes A and B (5 and 6), were characterized from the culture extract of the cold-seep derived fungus Furcasterigmium furcatum CS-280 co-cultured with autoclaved Pseudomonas aeruginosa QDIO-4. All the six compounds were highly oxygenated especially 2 and 3 with infrequent epoxyethane and tetrahydrofuran ring systems. The structures of 1-6 were established on the basis of detailed interpretation of 1D and 2D NMR and MS data. Their relative and absolute configurations were assigned by a combination of NOESY and single crystal X-ray crystallographic analysis, and by time-dependent density functional (TDDFT) ECD calculations as well. All compounds were tested the anti-inflammatory activity against human COX-2 protein, among which, compounds 2 and 3 displayed activities with IC50 values 123.00 µM and 93.45 µM, respectively. The interaction mechanism was interpreted by molecular docking.

Keywords: Furcasterigmium furcatum; acorane; cold-seep derived fungus; eremophilane; sesquiterpenes.

MeSH terms

  • Anti-Inflammatory Agents / chemistry
  • Anti-Inflammatory Agents / isolation & purification
  • Anti-Inflammatory Agents / pharmacology
  • Crystallography, X-Ray
  • Cyclooxygenase 2 / metabolism
  • Cyclooxygenase 2 Inhibitors / chemistry
  • Cyclooxygenase 2 Inhibitors / isolation & purification
  • Cyclooxygenase 2 Inhibitors / pharmacology
  • Humans
  • Molecular Docking Simulation
  • Polycyclic Sesquiterpenes / chemistry
  • Polycyclic Sesquiterpenes / isolation & purification
  • Polycyclic Sesquiterpenes / pharmacology
  • Pseudomonas aeruginosa* / drug effects
  • Sesquiterpenes* / chemistry
  • Sesquiterpenes* / isolation & purification
  • Sesquiterpenes* / pharmacology

Substances

  • Sesquiterpenes
  • Anti-Inflammatory Agents
  • Polycyclic Sesquiterpenes
  • Cyclooxygenase 2
  • eremophilane compounds
  • Cyclooxygenase 2 Inhibitors