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6T6B

Crystal structure of PPARgamma in complex with compound 16 (MF27)

Summary for 6T6B
Entry DOI10.2210/pdb6t6b/pdb
DescriptorPeroxisome proliferator-activated receptor gamma, (2~{R})-2-[[6-[(2,4-dichlorophenyl)sulfonylamino]-1,3-benzothiazol-2-yl]sulfanyl]octanoic acid (3 entities in total)
Functional Keywordspparg, peroxisome proliferator activated receptor gamma, inhibitor, structural genomics, structural genomics consortium, sgc, dna binding protein
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight32201.30
Authors
Chaikuad, A.,Ni, X.,Hanke, T.,Arrowsmith, C.H.,Edwards, A.M.,Bountra, C.,Merk, D.,Knapp, S.,Structural Genomics Consortium (SGC) (deposition date: 2019-10-18, release date: 2019-12-11, Last modification date: 2024-01-24)
Primary citationHanke, T.,Cheung, S.Y.,Kilu, W.,Heering, J.,Ni, X.,Planz, V.,Schierle, S.,Faudone, G.,Friedrich, M.,Wanior, M.,Werz, O.,Windbergs, M.,Proschak, E.,Schubert-Zsilavecz, M.,Chaikuad, A.,Knapp, S.,Merk, D.
A Selective Modulator of Peroxisome Proliferator-Activated Receptor gamma with an Unprecedented Binding Mode.
J.Med.Chem., 63:4555-4561, 2020
Cited by
PubMed Abstract: The nuclear peroxisome proliferator-activated receptor γ has well-validated therapeutic potential in metabolic, inflammatory, and neurodegenerative pathologies, but its activation is also associated with marked adverse effects and novel modes of PPARγ modulation are required. Here, we report the discovery and profiling of a new PPARγ modulator chemotype endowed with remarkable potency and a distinct binding mode in the orthosteric PPARγ ligand-binding site. Its -enantiomer evolved as a eutomer regarding PPARγ activation with a high eudysmic ratio. The new PPARγ modulator revealed outstanding selectivity over the PPARα and PPARδ subtypes and did not promote adipogenesis in primary human fibroblasts, discriminating it from established agonists.
PubMed: 32267688
DOI: 10.1021/acs.jmedchem.9b01786
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.8 Å)
Structure validation

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