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TitleNovel highly selective peroxisome proliferator-activated receptor delta (PPAR delta) modulators with pharmacokinetic properties suitable for once-daily oral dosing.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 27, Page 5230-5234, Year 2017
Publish dateMay 16, 2017 (structure data deposition date)
AuthorsLagu, B. / Kluge, A.F. / Fredenburg, R.A. / Tozzo, E. / Senaiar, R.S. / Jaleel, M. / Panigrahi, S.K. / Tiwari, N.K. / Krishnamurthy, N.R. / Takahashi, T. / Patane, M.A.
External linksBioorg. Med. Chem. Lett. / PubMed:29103972
MethodsX-ray diffraction
Resolution2 Å
Structure data

PDB-5xmx:
Co-crystal structure of Inhibitor compound in complex with human PPARdelta LBD
Method: X-RAY DIFFRACTION / Resolution: 2 Å

Chemicals

ChemComp-89L:
(E)-6-[2-[[[4-(furan-2-yl)phenyl]carbonyl-methyl-amino]methyl]phenoxy]-4-methyl-hex-4-enoic acid

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSCRIPTION/INHIBITOR / PPARdelta / Inhibitor compound / TRANSCRIPTION-INHIBITOR complex

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