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TitleDesign, Synthesis, and Evaluation of a Novel Series of Indole Sulfonamide Peroxisome Proliferator Activated Receptor (PPAR) alpha / gamma / delta Triple Activators: Discovery of Lanifibranor, a New Antifibrotic Clinical Candidate.
Journal, issue, pagesJ. Med. Chem., Vol. 61, Page 2246-2265, Year 2018
Publish dateOct 6, 2017 (structure data deposition date)
AuthorsBoubia, B. / Poupardin, O. / Barth, M. / Binet, J. / Peralba, P. / Mounier, L. / Jacquier, E. / Gauthier, E. / Lepais, V. / Chatar, M. ...Boubia, B. / Poupardin, O. / Barth, M. / Binet, J. / Peralba, P. / Mounier, L. / Jacquier, E. / Gauthier, E. / Lepais, V. / Chatar, M. / Ferry, S. / Thourigny, A. / Guillier, F. / Llacer, J. / Amaudrut, J. / Dodey, P. / Lacombe, O. / Masson, P. / Montalbetti, C. / Wettstein, G. / Luccarini, J.M. / Legendre, C. / Junien, J.L. / Broqua, P.
External linksJ. Med. Chem. / PubMed:29446942
MethodsX-ray diffraction
Resolution2.2 Å
Structure data

PDB-6enq:
Structure of human PPAR gamma LBD in complex with Lanifibranor (IVA337)
Method: X-RAY DIFFRACTION / Resolution: 2.2 Å

Chemicals

ChemComp-BJB:
4-[1-(1,3-benzothiazol-6-ylsulfonyl)-5-chloro-indol-2-yl]butanoic acid

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSCRIPTION / Nuclear hormone receptor / PPARgamma modulator / Lanifibranor

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