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5G5W

Structure guided design and discovery of Indazole ethers as highly potent, non-steroidal Glucocorticoid receptor modulators

Summary for 5G5W
Entry DOI10.2210/pdb5g5w/pdb
DescriptorGLUCOCORTICOID RECEPTOR, NUCLEAR RECEPTOR COACTIVATOR 2, 1,2-ETHANEDIOL, ... (5 entities in total)
Functional Keywordshormone, glucocorticoid receptor, nuclear hormone receptor, steroid receptor, signaling protein, ligand complex, peptide complex
Biological sourceHOMO SAPIENS (HUMAN)
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Total number of polymer chains2
Total formula weight34415.56
Authors
Primary citationHemmerling, M.,Edman, K.,Lepisto, M.,Eriksson, A.,Ivanova, S.,Dahmen, J.,Rehwinkel, H.,Berger, M.,Hendrickx, R.,Dearman, M.,Jensen, T.J.,Wissler, L.,Hansson, T.
Discovery of Indazole Ethers as Novel, Potent, Non-Steroidal Glucocorticoid Receptor Modulators.
Bioorg.Med.Chem.Lett., 26:5741-, 2017
Cited by
PubMed Abstract: A structure-based design approach led to the identification of a novel class of indazole ether based, non-steroidal glucocorticoid receptor (GR) modulators. Several examples were identified that displayed cell potency in the picomolar range, inhibiting LPS-induced TNF-α release by primary peripheral blood mononuclear cells (PBMCs). Additionally, an improved steroid hormone receptor binding selectivity profile, compared to classical steroidal GR agonists, was demonstrated. The indazole ether core tolerated a broad range of substituents allowing for modulation of the physiochemical parameters. A small sub-set of indazole ethers, with pharmacokinetic properties suitable for oral administration, was investigated in a rat antigen-induced joint inflammation model and demonstrated excellent anti-inflammatory efficacy.
PubMed: 27810243
DOI: 10.1016/J.BMCL.2016.10.052
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.2 Å)
Structure validation

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