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Ligands
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9LU 6-[2-({2-[4-(furan-2-yl)phenyl]-5-methyl-1h-imidazol-1-yl}methyl)phenoxy]hexanoic acid
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Code : 5ZXI   PDBj   RCSB PDB   PDBe
Header : TRANSCRIPTION
Title : Co-crystal structure of an Inhibitor in complex with human PPARdelta LBD
Release Data : 2019-04-03
Compound :
mol_id molecule chains synonym
1 Peroxisome proliferator-activated receptor delta A,B PPAR-delta,NUCI,Nuclear hormone receptor 1,NUC1,Nuclear receptor subfamily 1 group C member 2,Peroxisome proliferator-activated receptor beta,PPAR-beta
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Escherichia coli K-12  (taxid:83333)
gene: PPARD, NR1C2, PPARB
Authors : Rani, S.T., Laxminarasimhan, A., Senaiar, R.S., Krishnamurthy, N.
Keywords : PPARdelta, Inhibitor compound Co-Crystal structure, TRANSCRIPTION
Exp. method : X-RAY DIFFRACTION ( 2.10 Å )
Citation :

Selective PPAR delta Modulators Improve Mitochondrial Function: Potential Treatment for Duchenne Muscular Dystrophy (DMD).

Lagu, B.,Kluge, A.F.,Tozzo, E.  et al.
(2018)  ACS Med Chem Lett  9 : 935 - 940

PubMed: 30258544
DOI: 10.1021/acsmedchemlett.8b00287

Chain : A, B
UniProt : Q03181 (PPARD_HUMAN)
Reaction : -