GW3965 [Ligand Id: 2754] activity data from GtoPdb and ChEMBL

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ChEMBL ligand: CHEMBL59030 (GW3965)
  • Liver X receptor-α/LXR-alpha in Human [ChEMBL: CHEMBL2808] [GtoPdb: 602] [UniProtKB: Q13133]
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  • Retinoid X receptor-α/Liver X receptor-β/Retinoic acid receptor RXR-alpha/oxysterols receptor LXR-beta in Human [ChEMBL: CHEMBL3430878] [GtoPdb: 610601] [UniProtKB: P19793P55055]
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DB Assay description Assay Type Standard value Standard parameter Original value Original units Original parameter Reference
Liver X receptor-α/LXR-alpha in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2808] [GtoPdb: 602] [UniProtKB: Q13133]
ChEMBL Binding affinity to full-length human LXRalpha by surface plasmon resonance assay B 5.16 pKd 6970 nM Kd J Med Chem (2021) 64: 9943-9959 [PMID:34251816]
ChEMBL Displacement of [N-methyl-3H]GW0438 from human biotinylated LXRalpha ligand binding domain B 6.63 pIC50 235 nM IC50 J Med Chem (2008) 51: 5758-5765 [PMID:18800767]
ChEMBL Displacement of [3H]T-0901317 from human LXR alpha receptor B 7 pIC50 100 nM IC50 J Med Chem (2006) 49: 6151-6154 [PMID:17034119]
ChEMBL Displacement of [3H]TO901317 from human recombinant LXRalpha expressed in Escherichia coli by flashplate method B 7 pIC50 100 nM IC50 J Med Chem (2008) 51: 7161-7168 [PMID:18973288]
ChEMBL Antagonist activity at LXRalpha ligand binding domain assessed as inhibition of T1317-induced transcriptional activity in african green monkey CV1 cells co-transfected with Gal4-SRC1 by luciferase reporter assay B 7 pIC50 100 nM IC50 J Med Chem (2010) 53: 3412-3416 [PMID:20345102]
ChEMBL Agonist activity at LXRalpha (unknown origin) B 5.89 pEC50 1300 nM EC50 Bioorg Med Chem Lett (2015) 25: 2668-2674 [PMID:25998501]
ChEMBL Agonist activity at Gal4-tagged LXRalpha (unknown origin) expressed in CHOK1 cells after 24 hrs by luciferase reporter gene assay B 5.89 pEC50 1300 nM EC50 Bioorg Med Chem Lett (2015) 25: 1274-1278 [PMID:25677664]
ChEMBL Agonist activity at human LXRalpha by Gal4 assay B 5.95 pEC50 1128 nM EC50 J Med Chem (2016) 59: 3264-3271 [PMID:26990539]
ChEMBL Agonist activity at LXRalpha ligand binding domain-mediated transcriptional activity in african green monkey CV1 cells co-transfected with Gal4-SRC1 by luciferase reporter assay B 6.1 pEC50 794.33 nM EC50 J Med Chem (2010) 53: 3412-3416 [PMID:20345102]
ChEMBL Agonist activity at human recombinant LXRalpha ligand binding domain in human HuH7 cells co-transfected with fused Gal4-DBD by transactivation assay B 6.18 pEC50 660 nM EC50 J Med Chem (2008) 51: 7161-7168 [PMID:18973288]
ChEMBL Agonist activity at LXRalpha LBD by HTRF cofactor peptide recruitment assay F 6.44 pEC50 367 nM EC50 Bioorg Med Chem Lett (2007) 17: 3473-3479 [PMID:17416521]
ChEMBL Agonist activity at human LXRalpha receptor after 1 hr by HTRF cofactor recruitment assay F 6.44 pEC50 367 nM EC50 Bioorg Med Chem Lett (2007) 17: 4442-4446 [PMID:17587573]
ChEMBL Agonist activity at human LXRalpha expressed in human SH-SY5Y cells co-transfected with Gal4-LBD after 24 hrs by luciferase reporter gene assay F 6.51 pEC50 310 nM EC50 Bioorg Med Chem Lett (2009) 19: 2009-2012 [PMID:19264481]
ChEMBL Agonist activity at LXRalpha ligand binding domain by FRET based SRC1 recruitment assay B 6.55 pEC50 280 nM EC50 Bioorg Med Chem Lett (2009) 19: 2009-2012 [PMID:19264481]
ChEMBL Agonist activity at human LXRalpha assessed as association of SRC1 to LXRalpha ligand binding domain by FRET based cell-free ligand sensing assay B 6.7 pEC50 200 nM EC50 Bioorg Med Chem Lett (2009) 19: 5617-5621 [PMID:19717304]
GtoPdb - - 6.7 pEC50 - - - J Med Chem (2002) 45: 1963-6 [PMID:11985463]
ChEMBL Effective concentration in LXR alpha-Gal4 receptor gene assay B 6.72 pEC50 190 nM EC50 J Med Chem (2002) 45: 1963-1966 [PMID:11985463]
ChEMBL Agonist activity at LXRalpha by FRET assay F 6.76 pEC50 175 nM EC50 Bioorg Med Chem Lett (2009) 19: 1097-1100 [PMID:19167885]
ChEMBL Ligand-dependent recruitment of steroid receptor co-activator 1 (SRC1) to Liver X receptor-alpha B 6.9 pEC50 125 nM EC50 J Med Chem (2002) 45: 1963-1966 [PMID:11985463]
ChEMBL Agonist activity at GAL-linked human LXRalpha expressed in THP1 cells assessed as stimulation of coactivator recruitment by FRET assay F 7.01 pEC50 97 nM EC50 J Med Chem (2007) 50: 4255-4259 [PMID:17665897]
ChEMBL Effective concentration for Steroid receptor coactivator-1 (SRC1) recruitment to human LXRalpha (Liver X receptor) B 7.1 pEC50 80 nM EC50 J Med Chem (2005) 48: 5419-5422 [PMID:16107141]
ChEMBL Activity at human LXRalpha by Gal4 transactivation assay B 7.18 pEC50 66 nM EC50 J Med Chem (2007) 50: 4255-4259 [PMID:17665897]
ChEMBL Binding affinity to human LXRalpha B 7.66 pEC50 22 nM EC50 J Med Chem (2016) 59: 3264-3271 [PMID:26990539]
Liver X receptor-β/LXR-beta in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4093] [GtoPdb: 601] [UniProtKB: P55055]
ChEMBL Binding affinity to recombinant human LXRbeta-LBD expressed in Escherichia coli BL21 (DE3) assessed as inhibitory constant incubated for 30 mins by fluorescence polarization binding assay B 8.66 pKi 2.2 nM Ki Eur J Med Chem (2019) 178: 458-467 [PMID:31202993]
ChEMBL Displacement of hyodeoxycholicacid-based fluorescent tracer from recombinant human LXRbeta LBD (215 to 461 residues) expressed in Escherichia coli BL21 (DE3) preincubated for 10 mins under shaking condition and measured after 30 mins by fluorescence polarization assay B 8.66 pKi 2.2 nM Ki Eur J Med Chem (2020) 194: 112240-112240 [PMID:32248003]
ChEMBL Antagonist activity at LXRbeta ligand binding domain assessed as inhibition of T1317-induced transcriptional activity in african green monkey CV1 cells co-transfected with Gal4-SRC1 by luciferase reporter assay B 7.4 pIC50 39.81 nM IC50 J Med Chem (2010) 53: 3412-3416 [PMID:20345102]
ChEMBL Displacement of [N-methyl-3H]GW0438 from human biotinylated LXRbeta ligand binding domain B 7.52 pIC50 30 nM IC50 J Med Chem (2008) 51: 5758-5765 [PMID:18800767]
ChEMBL Displacement of [3H]T-0901317 from human LXR beta receptor B 7.92 pIC50 12 nM IC50 J Med Chem (2006) 49: 6151-6154 [PMID:17034119]
ChEMBL Displacement of [3H]TO901317 from human recombinant LXRbeta expressed in Escherichia coli by flashplate method B 7.92 pIC50 12 nM IC50 J Med Chem (2008) 51: 7161-7168 [PMID:18973288]
ChEMBL Displacement of [N-methyl-3H]T1317 from human biotinylated LXRbeta LBD after 3 hrs by LEAD seeker binding assay B 8.1 pIC50 7.94 nM IC50 J Med Chem (2010) 53: 3412-3416 [PMID:20345102]
ChEMBL Agonist activity at LXRbeta ligand binding domain-mediated transcriptional activity in african green monkey CV1 cells co-transfected with Gal4-SRC1 by luciferase reporter assay B 6.3 pEC50 501.19 nM EC50 J Med Chem (2010) 53: 3412-3416 [PMID:20345102]
ChEMBL Agonist activity at Gal4-tagged LXRbeta (unknown origin) expressed in CHOK1 cells after 24 hrs by luciferase reporter gene assay B 6.38 pEC50 420 nM EC50 Bioorg Med Chem Lett (2015) 25: 1274-1278 [PMID:25677664]
ChEMBL Agonist activity at human LXR beta receptor expressed in CHO cells by reporter assay F 6.39 pEC50 410 nM EC50 J Med Chem (2006) 49: 6151-6154 [PMID:17034119]
ChEMBL Agonist activity at LXRbeta (unknown origin) B 6.4 pEC50 400 nM EC50 Bioorg Med Chem Lett (2015) 25: 2668-2674 [PMID:25998501]
ChEMBL Agonist activity at human LXRbeta by Gal4 assay B 6.41 pEC50 390 nM EC50 J Med Chem (2016) 59: 3264-3271 [PMID:26990539]
ChEMBL Agonist activity at human recombinant LXRbeta ligand binding domain in human HuH7 cells co-transfected with fused Gal4-DBD by transactivation assay B 6.51 pEC50 310 nM EC50 J Med Chem (2008) 51: 7161-7168 [PMID:18973288]
ChEMBL Agonist activity at recombinant human LXRbeta-LBD expressed in Escherichia coli BL21 (DE3) assessed as peptide D22 recruitment fluorescence polarization binding assay B 6.54 pEC50 289 nM EC50 Eur J Med Chem (2019) 178: 458-467 [PMID:31202993]
ChEMBL Agonist activity at human LXRbeta expressed in human SH-SY5Y cells co-transfected with Gal4-LBD after 24 hrs by luciferase reporter gene assay F 6.89 pEC50 130 nM EC50 Bioorg Med Chem Lett (2009) 19: 2009-2012 [PMID:19264481]
ChEMBL Agonist activity at LXRbeta ligand binding domain by FRET based SRC1 recruitment assay B 7.11 pEC50 78 nM EC50 Bioorg Med Chem Lett (2009) 19: 2009-2012 [PMID:19264481]
ChEMBL Agonist activity at human LXRbeta assessed as association of SRC1 to LXRbeta ligand binding domain by FRET based cell-free ligand sensing assay B 7.4 pEC50 40 nM EC50 Bioorg Med Chem Lett (2009) 19: 5617-5621 [PMID:19717304]
ChEMBL Agonist activity at LXRbeta LBD by HTRF cofactor peptide recruitment assay F 7.46 pEC50 35 nM EC50 Bioorg Med Chem Lett (2007) 17: 3473-3479 [PMID:17416521]
ChEMBL Agonist activity at human LXRbeta receptor after 1 hr by HTRF cofactor recruitment assay F 7.46 pEC50 35 nM EC50 Bioorg Med Chem Lett (2007) 17: 4442-4446 [PMID:17587573]
GtoPdb - - 7.52 pEC50 - - - J Med Chem (2002) 45: 1963-6 [PMID:11985463]
ChEMBL Agonist activity at GAL-linked human LXRbeta expressed in THP1 cells assessed as stimulation of co-activator recruitment by FRET assay F 7.57 pEC50 27 nM EC50 J Med Chem (2007) 50: 4255-4259 [PMID:17665897]
ChEMBL Agonist activity at LXRbeta by FRET assay F 7.6 pEC50 25 nM EC50 Bioorg Med Chem Lett (2009) 19: 1097-1100 [PMID:19167885]
ChEMBL Effective concentration for Steroid receptor coactivator-1 (SRC1) recruitment to human LXRbeta (Liver X receptor) B 7.7 pEC50 20 nM EC50 J Med Chem (2005) 48: 5419-5422 [PMID:16107141]
ChEMBL Agonist activity at human LXRbeta receptor transfected in COS7 cells after 16 hrs by reporter transactivation assay F 7.82 pEC50 15 nM EC50 Bioorg Med Chem Lett (2007) 17: 4442-4446 [PMID:17587573]
ChEMBL Activation of LXRbeta co-transfected in COS7 cells with RXRalpha by reporter transactivation assay F 7.82 pEC50 15 nM EC50 Bioorg Med Chem Lett (2007) 17: 3473-3479 [PMID:17416521]
ChEMBL Binding to human LXRbeta B 8.3 pEC50 5 nM EC50 J Med Chem (2016) 59: 3264-3271 [PMID:26990539]
ChEMBL Activity at human LXRbeta by Gal4 transactivation assay B 8.4 pEC50 4 nM EC50 J Med Chem (2007) 50: 4255-4259 [PMID:17665897]
Pregnane X receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3401] [GtoPdb: 606] [UniProtKB: O75469]
ChEMBL Binding affinity to PXR by scintillation proximity binding assay B 5.7 pKi 2000 nM Ki Bioorg Med Chem Lett (2009) 19: 5617-5621 [PMID:19717304]
Retinoid X receptor-α/Liver X receptor-β/Retinoic acid receptor RXR-alpha/oxysterols receptor LXR-beta in Human (target type: PROTEIN COMPLEX) [ChEMBL: CHEMBL3430878] [GtoPdb: 610601] [UniProtKB: P19793P55055]
GtoPdb - - 7.52 pEC50 - - - J Med Chem (2002) 45: 1963-6 [PMID:11985463]
ChEMBL Agonist activity at human RXRalpha/LXRbeta expressed in HEK293 cells measured after 20 hrs by dual luciferase reporter gene assay B 9.64 pEC50 0.23 nM EC50 Eur J Med Chem (2020) 194: 112240-112240 [PMID:32248003]

ChEMBL data shown on this page come from version 33:

Mendez D, Gaulton A, Bento AP, Chambers J, De Veij M, Félix E, Magariños MP, Mosquera JF, Mutowo P, Nowotka M, Gordillo-Marañón M, Hunter F, Junco L, Mugumbate G, Rodriguez-Lopez M, Atkinson F, Bosc N, Radoux CJ, Segura-Cabrera A, Hersey A, Leach AR. (2019) 'ChEMBL: towards direct deposition of bioassay data' Nucleic Acids Res., 47(D1). DOI: 10.1093/nar/gky1075. [EPMCID:30398643]
Davies M, Nowotka M, Papadatos G, Dedman N, Gaulton A, Atkinson F, Bellis L, Overington JP. (2015) 'ChEMBL web services: streamlining access to drug discovery data and utilities.' Nucleic Acids Res., 43(W1). DOI: 10.1093/nar/gkv352. [EPMCID:25883136]