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Structure paper

TitleAryl and Arylalkyl Substituted 3-Hydroxypyridin-2(1H)-ones: Synthesis and Evaluation as Inhibitors of Influenza A Endonuclease.
Journal, issue, pagesChemmedchem, Vol. 14, Page 1204-1223, Year 2019
Publish dateDec 17, 2018 (structure data deposition date)
AuthorsSagong, H.Y. / Bauman, J.D. / Nogales, A. / Martinez-Sobrido, L. / Arnold, E. / LaVoie, E.J.
External linksChemmedchem / PubMed:30983160
MethodsX-ray diffraction
Resolution1.95 - 2 Å
Structure data

PDB-6nel:
4-(2-(4-fluorophenyl)-5-hydroxy-6-oxo-1,6-dihydropyridin-3-yl)benzoic acid bound to influenza 2009 pH1N1 endonuclease
Method: X-RAY DIFFRACTION / Resolution: 2 Å

PDB-6nem:
3-hydroxy-5-[(naphthalen-1-yl)methyl]-6-[4-(1H-tetrazol-5-yl)phenyl]pyridin-2(1H)-one bound to influenza 2009 pH1N1 endonuclease
Method: X-RAY DIFFRACTION / Resolution: 1.95 Å

Chemicals

ChemComp-MN:
Unknown entry

ChemComp-MG:
Unknown entry

ChemComp-KKV:
4-[2-(4-fluorophenyl)-5-hydroxy-6-oxo-1,6-dihydropyridin-3-yl]benzoic acid

ChemComp-SO4:
SULFATE ION

ChemComp-HOH:
WATER

ChemComp-KKS:
3-hydroxy-5-[(naphthalen-1-yl)methyl]-6-[4-(1H-tetrazol-5-yl)phenyl]pyridin-2(1H)-one

Source
  • influenza a virus
KeywordsVIRAL PROTEIN/INHIBITOR / Influenza endonuclease inhibitor chelator / VIRAL PROTEIN / VIRAL PROTEIN-INHIBITOR complex

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