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10.1021/acs.jmedchem.7b00259

http://scihub22266oqcxt.onion/10.1021/acs.jmedchem.7b00259
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suck abstract from ncbi


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pmid28422508
      J+Med+Chem 2017 ; 60 (9 ): 3958-3978
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  • Nitrile in the Hole: Discovery of a Small Auxiliary Pocket in Neuronal Nitric Oxide Synthase Leading to the Development of Potent and Selective 2-Aminoquinoline Inhibitors #MMPMID28422508
  • Cinelli MA ; Li H ; Chreifi G ; Poulos TL ; Silverman RB
  • J Med Chem 2017[May]; 60 (9 ): 3958-3978 PMID28422508 show ga
  • Neuronal nitric oxide synthase (nNOS) inhibition is a promising strategy to treat neurodegenerative disorders, but the development of nNOS inhibitors is often hindered by poor pharmacokinetics. We previously developed a class of membrane-permeable 2-aminoquinoline inhibitors and later rearranged the scaffold to decrease off-target binding. However, the resulting compounds had decreased permeability, low human nNOS activity, and low selectivity versus human eNOS. In this study, 5-substituted phenyl ether-linked aminoquinolines and derivatives were synthesized and assayed against purified NOS isoforms. 5-Cyano compounds are especially potent and selective rat and human nNOS inhibitors. Activity and selectivity are mediated by the binding of the cyano group to a new auxiliary pocket in nNOS. Potency was enhanced by methylation of the quinoline and by introduction of simple chiral moieties, resulting in a combination of hydrophobic and auxiliary pocket effects that yielded high (?500-fold) n/e selectivity. Importantly, the Caco-2 assay also revealed improved membrane permeability over previous compounds.
  • |Aminoquinolines/*pharmacology [MESH]
  • |Animals [MESH]
  • |Drug Discovery [MESH]
  • |Enzyme Inhibitors/chemistry/*pharmacology [MESH]
  • |Humans [MESH]
  • |Nitric Oxide Synthase Type I/*antagonists & inhibitors/*chemistry [MESH]
  • |Nitriles/*chemistry [MESH]


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