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Unveiling (−)‐Englerin A as a Modulator of L‐Type Calcium Channels
Author(s) -
Rodrigues Tiago,
Sieglitz Florian,
Somovilla Víctor J.,
Cal Pedro M. S. D.,
Galione Antony,
Corzana Francisco,
Bernardes Gonçalo J. L.
Publication year - 2016
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201604336
Subject(s) - pharmacophore , chemistry , natural product , ligand (biochemistry) , l type calcium channel , dihydropyridine , molecular dynamics , macromolecule , biophysics , voltage dependent calcium channel , calcium , stereochemistry , biochemistry , biology , receptor , computational chemistry , organic chemistry
The voltage‐dependent L‐type Ca 2+ channel was identified as a macromolecular target for (−)‐englerin A. This finding was reached by using an unprecedented ligand‐based prediction platform and the natural product piperlongumine as a pharmacophore probe. (−)‐Englerin A features high substructure dissimilarity to known ligands for voltage‐dependent Ca 2+ channels, selective binding affinity for the dihydropyridine site, and potent modulation of calcium signaling in muscle cells and vascular tissue. The observed activity was rationalized at the atomic level by molecular dynamics simulations. Experimental confirmation of this hitherto unknown macromolecular target expands the bioactivity space for this natural product and corroborates the effectiveness of chemocentric computational methods for prioritizing target‐based screens and identifying binding counterparts of complex natural products.