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Found 115 with Last Name = 'fletterick' and Initial = 'rj'
TargetAndrogen receptor(Homo sapiens (Human))
The Regents of The University of California

US Patent
LigandPNGBDBM238895(US10053433, Casodex (CDX) | US10053433, FC 4.037 (...)
Affinity DataIC50:  15nMpH: 7.5Assay Description:Briefly, the AR LBD is expressed as a fusion with the Gal4 transcription factor, which binds to the Gal4 reporter DNA. Upon activation with agonist h...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetAndrogen receptor(Homo sapiens (Human))
The Regents of The University of California

US Patent
LigandPNGBDBM238895(US10053433, Casodex (CDX) | US10053433, FC 4.037 (...)
Affinity DataIC50:  190nMpH: 7.5Assay Description:An AR-response element is contained within the mmTV sequence and drives the expression of luciferase. The effect of antiandrogens (competitive antago...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetAndrogen receptor(Homo sapiens (Human))
The Regents of The University of California

US Patent
LigandPNGBDBM238895(US10053433, Casodex (CDX) | US10053433, FC 4.037 (...)
Affinity DataIC50:  360nMpH: 7.5Assay Description:Briefly, the AR LBD is expressed as a fusion with the Gal4 transcription factor, which binds to the Gal4 reporter DNA. Upon activation with agonist h...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetAndrogen receptor(Homo sapiens (Human))
The Regents of The University of California

US Patent
LigandPNGBDBM239191(US10053433, FC 3.077)
Affinity DataIC50:  490nMpH: 7.5Assay Description:Briefly, the AR LBD is expressed as a fusion with the Gal4 transcription factor, which binds to the Gal4 reporter DNA. Upon activation with agonist h...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetAndrogen receptor(Homo sapiens (Human))
The Regents of The University of California

US Patent
LigandPNGBDBM242618(US10053433, FC 4.025)
Affinity DataIC50:  580nMpH: 7.5Assay Description:Briefly, the AR LBD is expressed as a fusion with the Gal4 transcription factor, which binds to the Gal4 reporter DNA. Upon activation with agonist h...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetAndrogen receptor(Homo sapiens (Human))
The Regents of The University of California

US Patent
LigandPNGBDBM242588(US10053433, FC 4.039)
Affinity DataIC50:  750nMpH: 7.5Assay Description:Briefly, the AR LBD is expressed as a fusion with the Gal4 transcription factor, which binds to the Gal4 reporter DNA. Upon activation with agonist h...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetAndrogen receptor(Homo sapiens (Human))
The Regents of The University of California

US Patent
LigandPNGBDBM238895(US10053433, Casodex (CDX) | US10053433, FC 4.037 (...)
Affinity DataIC50:  1.00E+3nMpH: 7.5Assay Description:An AR-response element is contained within the mmTV sequence and drives the expression of luciferase. The effect of antiandrogens (competitive antago...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetGlutamate receptor 2(Homo sapiens (Human))
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50253632(6-Azido-7-nitro-1,4-dihydroquinoxaline-2,3-dione |...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibition of GluR2 receptor (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
The Regents of The University of California

US Patent
LigandPNGBDBM242618(US10053433, FC 4.025)
Affinity DataIC50:  1.29E+3nMpH: 7.5Assay Description:An AR-response element is contained within the mmTV sequence and drives the expression of luciferase. The effect of antiandrogens (competitive antago...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetThyroid hormone receptor beta [209-461](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18814(1-(4-hexylphenyl)-3-[methyl(2-phenylethyl)amino]pr...)
Affinity DataIC50:  1.50E+3nMAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor beta [209-461](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18825(1-(4-hexylphenyl)prop-2-en-1-one | Enone, 1)
Affinity DataIC50:  1.50E+3nMAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
TargetAndrogen receptor(Homo sapiens (Human))
The Regents of The University of California

US Patent
LigandPNGBDBM239363(US10053433, FC 4.126)
Affinity DataIC50:  1.55E+3nMpH: 7.5Assay Description:Briefly, the AR LBD is expressed as a fusion with the Gal4 transcription factor, which binds to the Gal4 reporter DNA. Upon activation with agonist h...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetThyroid hormone receptor beta [209-461](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18815(1-(4-hexylphenyl)-3-[(2-hydroxyethyl)(methyl)amino...)
Affinity DataIC50:  1.60E+3nMAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
The Regents of The University of California

US Patent
LigandPNGBDBM50425732(ENZALUTAMIDE | US10053433, FC 4.129 | US10806720, ...)
Affinity DataIC50:  1.94E+3nMpH: 7.5Assay Description:Briefly, the AR LBD is expressed as a fusion with the Gal4 transcription factor, which binds to the Gal4 reporter DNA. Upon activation with agonist h...More data for this Ligand-Target Pair
In DepthDetails US PatentDrugBank

TargetThyroid hormone receptor beta [209-461](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18816(3-[bis(propan-2-yl)amino]-1-(4-hexylphenyl)propan-...)
Affinity DataIC50:  2.00E+3nMAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
The Regents of The University of California

US Patent
LigandPNGBDBM239316(US10053433, FC 4.116)
Affinity DataIC50:  2.53E+3nMpH: 7.5Assay Description:Briefly, the AR LBD is expressed as a fusion with the Gal4 transcription factor, which binds to the Gal4 reporter DNA. Upon activation with agonist h...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetThyroid hormone receptor beta [209-461](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18818(1-(4-hexylphenyl)-3-(morpholin-4-yl)propan-1-one |...)
Affinity DataIC50:  2.70E+3nMAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor beta [209-461](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18817(1-(4-hexylphenyl)-3-(pyrrolidin-1-yl)propan-1-one ...)
Affinity DataIC50:  2.70E+3nMAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor beta [209-461](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18857(3-bromo-1-(4-hexylphenyl)propan-1-one | beta-bromo...)
Affinity DataIC50:  3.00E+3nMAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor alpha [148-410](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18815(1-(4-hexylphenyl)-3-[(2-hydroxyethyl)(methyl)amino...)
Affinity DataIC50:  3.00E+3nMpH: 7.2 T: 2°CAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
The Regents of The University of California

US Patent
LigandPNGBDBM50094975(956104-40-8 | ARN-509 | JNJ-56021927 | US10053433,...)
Affinity DataIC50:  3.11E+3nMpH: 7.5Assay Description:Briefly, the AR LBD is expressed as a fusion with the Gal4 transcription factor, which binds to the Gal4 reporter DNA. Upon activation with agonist h...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetAndrogen receptor(Homo sapiens (Human))
The Regents of The University of California

US Patent
LigandPNGBDBM50094975(956104-40-8 | ARN-509 | JNJ-56021927 | US10053433,...)
Affinity DataIC50:  3.28E+3nMpH: 7.5Assay Description:Briefly, the AR LBD is expressed as a fusion with the Gal4 transcription factor, which binds to the Gal4 reporter DNA. Upon activation with agonist h...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetThyroid hormone receptor alpha [148-410](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18814(1-(4-hexylphenyl)-3-[methyl(2-phenylethyl)amino]pr...)
Affinity DataIC50:  3.60E+3nMpH: 7.2 T: 2°CAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor beta [209-461](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18819(beta-Aminophenylketone, 3f | methyl 1-[3-(4-hexylp...)
Affinity DataIC50:  3.90E+3nMAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor alpha [148-410](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18816(3-[bis(propan-2-yl)amino]-1-(4-hexylphenyl)propan-...)
Affinity DataIC50:  4.10E+3nMpH: 7.2 T: 2°CAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor alpha [148-410](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18818(1-(4-hexylphenyl)-3-(morpholin-4-yl)propan-1-one |...)
Affinity DataIC50:  4.10E+3nMpH: 7.2 T: 2°CAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor beta [209-461](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18820(3-(dibutylamino)-1-(4-hexylphenyl)propan-1-one | b...)
Affinity DataIC50:  4.20E+3nMAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor alpha [148-410](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18857(3-bromo-1-(4-hexylphenyl)propan-1-one | beta-bromo...)
Affinity DataIC50:  4.20E+3nMAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor beta [209-461](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18821(3-(dimethylamino)-1-(4-hexylphenyl)propan-1-one | ...)
Affinity DataIC50:  4.30E+3nMAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor alpha [148-410](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18817(1-(4-hexylphenyl)-3-(pyrrolidin-1-yl)propan-1-one ...)
Affinity DataIC50:  4.30E+3nMpH: 7.2 T: 2°CAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor beta [209-461](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18854(4-hexylphenyl prop-2-ynoate | Propiolic acid deriv...)
Affinity DataIC50:  6.20E+3nMAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor alpha [148-410](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18819(beta-Aminophenylketone, 3f | methyl 1-[3-(4-hexylp...)
Affinity DataIC50:  6.30E+3nMpH: 7.2 T: 2°CAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor alpha [148-410](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18820(3-(dibutylamino)-1-(4-hexylphenyl)propan-1-one | b...)
Affinity DataIC50:  6.90E+3nMpH: 7.2 T: 2°CAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
The Regents of The University of California

US Patent
LigandPNGBDBM242578(US10053433, FC 4.127)
Affinity DataIC50:  7.26E+3nMpH: 7.5Assay Description:Briefly, the AR LBD is expressed as a fusion with the Gal4 transcription factor, which binds to the Gal4 reporter DNA. Upon activation with agonist h...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetGlutamate receptor 2(Homo sapiens (Human))
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50253650(CHEMBL462490 | [1,2,5]oxadiazolo[3,4-g]quinoxaline...)
Affinity DataIC50:  7.60E+3nMAssay Description:Inhibition of GluR2 receptor (unknown origin)More data for this Ligand-Target Pair
TargetThyroid hormone receptor beta [209-461](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18827((2E)-1-(4-heptylphenyl)but-2-en-1-one | Enone, 4b)
Affinity DataIC50:  7.60E+3nMAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor beta [209-461](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18843(Substituted Acrylate, 6k | hexyl 2-(prop-2-enoylox...)
Affinity DataIC50:  8.20E+3nMAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
The Regents of The University of California

US Patent
LigandPNGBDBM50425732(ENZALUTAMIDE | US10053433, FC 4.129 | US10806720, ...)
Affinity DataIC50:  8.61E+3nMpH: 7.5Assay Description:An AR-response element is contained within the mmTV sequence and drives the expression of luciferase. The effect of antiandrogens (competitive antago...More data for this Ligand-Target Pair
In DepthDetails US PatentDrugBank

TargetAndrogen receptor(Homo sapiens (Human))
The Regents of The University of California

US Patent
LigandPNGBDBM242578(US10053433, FC 4.127)
Affinity DataIC50:  8.74E+3nMpH: 7.5Assay Description:An AR-response element is contained within the mmTV sequence and drives the expression of luciferase. The effect of antiandrogens (competitive antago...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetThyroid hormone receptor beta [209-461](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18838(4-heptylphenyl prop-2-enoate | Substituted Acrylat...)
Affinity DataIC50:  1.05E+4nMAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor alpha [148-410](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18821(3-(dimethylamino)-1-(4-hexylphenyl)propan-1-one | ...)
Affinity DataIC50:  1.06E+4nMpH: 7.2 T: 2°CAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor beta [209-461](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18839(4-octylphenyl prop-2-enoate | Substituted Acrylate...)
Affinity DataIC50:  1.14E+4nMAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor beta [209-461](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18822(3-[(furan-2-ylmethyl)(methyl)amino]-1-(4-hexylphen...)
Affinity DataIC50:  1.21E+4nMAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
The Regents of The University of California

US Patent
LigandPNGBDBM239363(US10053433, FC 4.126)
Affinity DataIC50:  1.24E+4nMpH: 7.5Assay Description:An AR-response element is contained within the mmTV sequence and drives the expression of luciferase. The effect of antiandrogens (competitive antago...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetThyroid hormone receptor beta [209-461](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18823(3-(dicyclohexylamino)-1-(4-hexylphenyl)propan-1-on...)
Affinity DataIC50:  1.27E+4nMAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor beta [209-461](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18824(1-(4-hexylphenyl)-3-(propylamino)propan-1-one | be...)
Affinity DataIC50:  1.52E+4nMAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor alpha [148-410](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18823(3-(dicyclohexylamino)-1-(4-hexylphenyl)propan-1-on...)
Affinity DataIC50:  1.65E+4nMpH: 7.2 T: 2°CAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor alpha [148-410](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18854(4-hexylphenyl prop-2-ynoate | Propiolic acid deriv...)
Affinity DataIC50:  1.67E+4nMAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor alpha [148-410](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18847((2Z)-3-[(4-hexylphenyl)carbamoyl]prop-2-enoic acid...)
Affinity DataIC50:  1.75E+4nMAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThyroid hormone receptor beta [209-461](Homo sapiens (Human))
St. Jude Research Hospital

LigandPNGBDBM18826((2E)-4-(4-hexylphenyl)-4-oxobut-2-enoic acid | Eno...)
Affinity DataIC50:  1.77E+4nMAssay Description:IC50 is the concentration of each compound required to inhibit 50% of the binding between the TR LBD and the SRC2-2 peptide using fluorescence polari...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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