| Literature DB >> 27510286 |
Matthew D Hartle1, Ryan J Hansen1, Blakely W Tresca1, Samuel S Prakel1, Lev N Zakharov1,2, Michael M Haley3, Michael D Pluth4, Darren W Johnson5.
Abstract
<span class="Chemical">Hydrogen sulfide (<span class="Chemical">H2 S) has emerged as a crucial biomolecule in physiology and cellular signaling. Key challenges associated with developing new chemical tools for understanding the biological roles of H2 S include developing platforms that enable reversible binding of this important biomolecule. The first synthetic small molecule receptor for the hydrosulfide anion, HS(-) , using only reversible, hydrogen-bonding interactions in a series of bis(ethynylaniline) derivatives, is reported. Binding constants of up to 90 300±8700 m(-1) were obtained in MeCN. The fundamental science of reversible sulfide binding, in this case featuring a key CH⋅⋅⋅S hydrogen bond, will expand the possibility for discovery of sulfide protein targets and molecular recognition agents.Entities:
Keywords: anion binding; gasotransmitters; molecular recognition; sulfide; supramolecular chemistry
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Year: 2016 PMID: 27510286 PMCID: PMC5144539 DOI: 10.1002/anie.201605757
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336