NMR fingerprints of the drug-like natural-product space identify iotrochotazine A: a chemical probe to study Parkinson's disease

Angew Chem Int Ed Engl. 2014 Jun 10;53(24):6070-4. doi: 10.1002/anie.201402239. Epub 2014 Apr 15.

Abstract

The NMR spectrum of a mixture of small molecules is a fingerprint of all of its components. Herein, we present an NMR fingerprint method that takes advantage of the fact that fractions contain simplified NMR profiles, with minimal signal overlap, to allow the identification of unique spectral patterns. The approach is exemplified in the identification of a novel natural product, iotrochotazine A (1), sourced from an Australian marine sponge Iotrochota sp. Compound 1 was used as a chemical probe in a phenotypic assay panel based on human olfactory neurosphere-derived cells (hONS) from idiopathic Parkinson's disease patients. Compound 1 at 1 μM was not cytotoxic but specifically affected the morphology and cellular distribution of lysosomes and early endosomes.

Keywords: NMR fingerprints; NMR spectroscopy; Parkinson’s disease; natural products; total synthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biological Products / chemistry*
  • Heterocyclic Compounds, 3-Ring / chemistry*
  • Heterocyclic Compounds, 3-Ring / pharmacology
  • Humans
  • Molecular Structure
  • Nuclear Magnetic Resonance, Biomolecular / methods
  • Olfactory Mucosa / drug effects
  • Olfactory Mucosa / pathology
  • Parkinson Disease / diagnosis
  • Parkinson Disease / pathology
  • Porifera / chemistry

Substances

  • Biological Products
  • Heterocyclic Compounds, 3-Ring
  • iotrochotazine A