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Title3-Substituted Quinolines as ROR gamma t Inverse Agonists.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 29, Page 1463-1470, Year 2019
Publish dateDec 5, 2018 (structure data deposition date)
AuthorsTanis, V.M. / Venkatesan, H. / Cummings, M.D. / Albers, M. / Kent Barbay, J. / Herman, K. / Kummer, D.A. / Milligan, C. / Nelen, M.I. / Nishimura, R. ...Tanis, V.M. / Venkatesan, H. / Cummings, M.D. / Albers, M. / Kent Barbay, J. / Herman, K. / Kummer, D.A. / Milligan, C. / Nelen, M.I. / Nishimura, R. / Schlueter, T. / Scott, B. / Spurlino, J. / Wolin, R. / Woods, C. / Xue, X. / Edwards, J.P. / Fourie, A.M. / Leonard, K.
External linksBioorg. Med. Chem. Lett. / PubMed:31010722
MethodsX-ray diffraction
Resolution2.90197076582 Å
Structure data

PDB-6nad:
Identification and biological evaluation of tertiary ALCOHOL-based inverse agonists of RORgt
Method: X-RAY DIFFRACTION / Resolution: 2.90197076582 Å

Chemicals

ChemComp-KHY:
(S)-(4-chloro-2-methoxy-3-{[4-(trifluoromethyl)piperidin-1-yl]methyl}quinolin-6-yl)(1,2-dimethyl-1H-imidazol-5-yl)[2-(trifluoromethyl)pyridin-4-yl]methanol

Source
  • homo sapiens (human)
KeywordsNUCLEAR PROTEIN / Nuclear Receptor RORgt

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