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TitleSynthesis and Biological Evaluation of New Triazolo- and Imidazolopyridine ROR gamma t Inverse Agonists.
Journal, issue, pagesChemMedChem, Vol. 11, Page 2640-2648, Year 2016
Publish dateOct 31, 2016 (structure data deposition date)
AuthorsHintermann, S. / Guntermann, C. / Mattes, H. / Carcache, D.A. / Wagner, J. / Vulpetti, A. / Billich, A. / Dawson, J. / Kaupmann, K. / Kallen, J. ...Hintermann, S. / Guntermann, C. / Mattes, H. / Carcache, D.A. / Wagner, J. / Vulpetti, A. / Billich, A. / Dawson, J. / Kaupmann, K. / Kallen, J. / Stringer, R. / Orain, D.
External linksChemMedChem / PubMed:27902884
MethodsX-ray diffraction
Resolution1.77 Å
Structure data

PDB-5m96:
Synthesis and biological evaluation of new triazolo and imidazolopyridine RORgt inverse agonists
Method: X-RAY DIFFRACTION / Resolution: 1.77 Å

Chemicals

ChemComp-Q6Y:
~{N}-[8-[[(3~{S})-4-cyclopentylcarbonyl-3-methyl-piperazin-1-yl]methyl]-7-methyl-imidazo[1,2-a]pyridin-6-yl]-2-methyl-pyrimidine-5-carboxamide

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSCRIPTION / nuclear hormone receptor / ligand-binding domain / inverse agonist

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