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Fragment-based design of 3-aminopyridine-derived amides as potent inhibitors of human nicotinamide phosphoribosyltransferase (NAMPT)

Academic Article
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Overview

authors

  • Dragovich, P. S.
  • Zhao, G.
  • Baumeister, T.
  • Bravo, B.
  • Giannetti, A. M.
  • Ho, Y. C.
  • Hua, R.
  • Li, G.
  • Liang, X.
  • Ma, X.
  • O'Brien, T.
  • Oh, A.
  • Skelton, N. J.
  • Wang, C.
  • Wang, W.
  • Wang, Y.
  • Xiao, Y.
  • Yuen, P. W.
  • Zak, Mark
  • Zhao, Q.
  • Zheng, X.

publication date

  • February 2014

journal

  • Bioorganic & Medicinal Chemistry Letters  Journal

subject areas

  • Amides
  • Aminopyridines
  • Antineoplastic Agents
  • Cell Proliferation
  • Cells, Cultured
  • Crystallography, X-Ray
  • Cytokines
  • Enzyme Activation
  • Enzyme Inhibitors
  • Humans
  • Inhibitory Concentration 50
  • Models, Molecular
  • Nicotinamide Phosphoribosyltransferase
  • Structure-Activity Relationship
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Research

keywords

  • Fragment-based design
  • NAMPT
  • Nicotinamide phosphoribosyltransferase
  • Structure-based design
  • Surface plasmon resonance
  • X-ray crystal structure
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Identity

International Standard Serial Number (ISSN)

  • 0960-894X

Digital Object Identifier (DOI)

  • 10.1016/j.bmcl.2013.12.062

PubMed ID

  • 24433859
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Additional Document Info

start page

  • 954

end page

  • 962

volume

  • 24

issue

  • 3

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