Marine Spirotetronates: Biosynthetic Edifices That Inspire Drug Discovery

Mar Drugs. 2019 Apr 19;17(4):232. doi: 10.3390/md17040232.

Abstract

Spirotetronates are actinomyces-derived polyketides that possess complex structures and exhibit potent and unexplored bioactivities. Due to their anticancer and antimicrobial properties, they have potential as drug hits and deserve further study. In particular, abyssomicin C and tetrocarcin A have shown significant promise against antibiotic-resistant S. aureus and tuberculosis, as well as for the treatment of various lymphomas and solid tumors. Improved synthetic routes to these compounds, particularly the class II spirotetronates, are needed to access sufficient quantities for structure optimization and clinical applications.

Keywords: Bcl-2 inhibitor; Diels-Alder; Diels-Alderase; UPR apoptosis; antibiotic; anticancer; biosynthesis; drug resistance; natural product; pABA inhibitor; spirotetronate; total synthesis.

Publication types

  • Review

MeSH terms

  • Aminoglycosides / chemistry*
  • Aminoglycosides / pharmacology
  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / pharmacology
  • Anti-Infective Agents / chemistry
  • Anti-Infective Agents / pharmacology
  • Bridged Bicyclo Compounds, Heterocyclic / chemistry*
  • Bridged Bicyclo Compounds, Heterocyclic / pharmacology
  • Drug Discovery
  • Humans
  • Methicillin-Resistant Staphylococcus aureus / drug effects
  • Polyketides / chemistry*
  • Polyketides / metabolism
  • Polyketides / pharmacology
  • Spiro Compounds / chemistry*
  • Spiro Compounds / metabolism
  • Spiro Compounds / pharmacology

Substances

  • Aminoglycosides
  • Anti-Bacterial Agents
  • Anti-Infective Agents
  • Bridged Bicyclo Compounds, Heterocyclic
  • Polyketides
  • Spiro Compounds
  • abyssomicin C
  • tetrocarcin A