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MMDB Description
18733Crystal Structure of the Ligand Binding Domain From Human Ppar-alpha in Complex With the Agonist AZ 242
18053The 2.5 Angstrom Resolution Crystal Structure of the Human Pparalpha Ligand Binding Domain Bound With Gw409544 and a Co-activator Peptide
71136Crystal Structure of the Human Ppar-alpha Ligand-binding Domain in Complex With an Antagonist Gw6471 and a Smrt Corepressor Motif
60106The Crystal Structure of the Human Pparaplpha Ligand Binding Domain in Complex With a A-hydroxyimino Phenylpropanoic Acid
45728a Crystal Structure of Ppar Alpha Bound With Src1 Peptide and Gw735
60944Crystal Structure of Pparalpha Ligand Binding Domain With Bms-631707
72409Human Pprr Alpha Ligand Binding Domain in Complex With a Synthetic Agonist Tipp703
69711Structure of Pparalpha With 3-[5-methoxy-1-(4-methoxy- Benzenesulfonyl)-1h-indol-3-yl]-propionic Acid
77468Design and Biological Evaluation of Novel, Balanced Dual Pparag Agonists
73050Aleglitazar, a New, Potent, and Balanced Ppar Alphagamma Agonist for the Treatment of Type II Diabetes
81691Crystal Structure of Peroxisome Proliferator-activatedecepto (Pparalpha) Complex With N-3-((2-(4-chlorophenyl)-5-methyl- Oxazol-4-yl)methoxy)benzyl)-n-(methoxycarbonyl)glycine
81692Crystal Structure of Peroxisome Proliferator-activatedecepto (Pparalpha) Complex With N-3-((2-(4-chlorophenyl)-5-methyl- Oxazol-4-yl)methoxy)benzyl)-n-((4-methylphenoxy)carbonyl)gl