Compile Data Set for Download or QSAR
Report error Found 358 of affinity data for UniProtKB/TrEMBL: O00482
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50605641(CHEMBL5177743)
Affinity DataKi:  0.150nMAssay Description:Binding affinity to N-terminal 6-His tagged human LRH-1 LBD (299 to 541 residues) expressed in Escherichia coli BL21-(DE3) assessed as inhibition con...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/25/2023
Entry Details
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50511469(CHEMBL4515639)
Affinity DataKd:  1nMAssay Description:Binding affinity to human LRH1 LBD (299 to 541 residues) expressed in Escherichia coli BL21 pLysS measured after overnight incubation by fluorescence...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50511467(CHEMBL4551205)
Affinity DataKi:  1.30nMAssay Description:Binding affinity to N-terminal 6-His tagged human LRH-1 LBD (299 to 541 residues) expressed in Escherichia coli BL21-(DE3) assessed as inhibition con...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/25/2023
Entry Details
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50511467(CHEMBL4551205)
Affinity DataKi:  2.10nMAssay Description:Displacement of 6N-FAM from human LRH1 LBD (299 to 541 residues) expressed in Escherichia coli BL21 pLysS by competitive binding based fluorescence p...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50511467(CHEMBL4551205)
Affinity DataKi:  2.70nMAssay Description:Displacement of 6N-FAM from LRH1 LBD (299 to 541 residues) expressed in Escherichia coli BL21 pLysS by competitive binding based fluorescence polariz...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50511469(CHEMBL4515639)
Affinity DataKd:  4.80nMAssay Description:Binding affinity to human apo-form LRH1 LBD (299 to 541 residues) expressed in Escherichia coli BL21 pLysS measured after overnight incubation by flu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50605640(CHEMBL5198453)
Affinity DataKi:  5.30nMAssay Description:Binding affinity to N-terminal 6-His tagged human LRH-1 LBD (299 to 541 residues) expressed in Escherichia coli BL21-(DE3) assessed as inhibition con...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/25/2023
Entry Details
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM22376((3aS,6aR)-4-cyclohexyl-5-[(4E)-oct-4-en-4-yl]-N-ph...)
Affinity DataEC50:  12nMpH: 7.5 T: 2°CAssay Description:The screen utilizes a ligand mediated co-factor interaction between purified bacterial expressed ligand binding domain of human LRH1 and a TIF2-deriv...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/29/2008
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50505369(CHEMBL4440757)
Affinity DataEC50:  15nMAssay Description:Agonist activity at human full length LRH1 transfected in human HeLa cells incubated for 24 hrs by renilla luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/18/2021
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50544056(CHEMBL4644327)
Affinity DataKi:  18nMAssay Description:Displacement of 6N-FAM from human LRH1 LBD (299 to 541 residues) expressed in Escherichia coli BL21 pLysS by competitive binding based fluorescence p...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM22375((3aS,6aR)-4-butyl-5-[(4E)-oct-4-en-4-yl]-N-phenyl-...)
Affinity DataEC50:  22nMpH: 7.5 T: 2°CAssay Description:The screen utilizes a ligand mediated co-factor interaction between purified bacterial expressed ligand binding domain of human LRH1 and a TIF2-deriv...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/29/2008
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM22391((3aS,6aR)-N-(2,3-dimethylphenyl)-5-hexyl-4-phenyl-...)
Affinity DataEC50:  30nMpH: 7.5 T: 2°CAssay Description:The screen utilizes a ligand mediated co-factor interaction between purified bacterial expressed ligand binding domain of human LRH1 and a TIF2-deriv...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/29/2008
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM22385((3aS,6aR)-5-hexyl-N,4-diphenyl-1,2,3,3a,6,6a-hexah...)
Affinity DataEC50:  31.6nMAssay Description:Agonist activity at human LRH-1 receptor assessed as TIF2 737-757 peptide recruitment by TR-FRET assay relative to controlMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM22385((3aS,6aR)-5-hexyl-N,4-diphenyl-1,2,3,3a,6,6a-hexah...)
Affinity DataEC50:  34nMpH: 7.5 T: 2°CAssay Description:The screen utilizes a ligand mediated co-factor interaction between purified bacterial expressed ligand binding domain of human LRH1 and a TIF2-deriv...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/29/2008
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50544057(CHEMBL4637563)
Affinity DataKi:  38nMAssay Description:Displacement of 6N-FAM from human LRH1 LBD (299 to 541 residues) expressed in Escherichia coli BL21 pLysS by competitive binding based fluorescence p...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50505372(CHEMBL4447391)
Affinity DataEC50:  40nMAssay Description:Agonist activity at human full length LRH1 transfected in human HeLa cells incubated for 24 hrs by renilla luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/18/2021
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50605641(CHEMBL5177743)
Affinity DataEC50:  43nMAssay Description:Agonist activity at LRH-1 (unknown origin) transfected in human HeLa cells measured after 24 hrs by Dual Glo luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/25/2023
Entry Details
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50544055(CHEMBL4645796)
Affinity DataKi:  56nMAssay Description:Displacement of 6N-FAM from human LRH1 LBD (299 to 541 residues) expressed in Escherichia coli BL21 pLysS by competitive binding based fluorescence p...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM22379((3aS,6aR)-4-(naphthalen-2-yl)-5-[(4E)-oct-4-en-4-y...)
Affinity DataEC50:  60nMpH: 7.5 T: 2°CAssay Description:The screen utilizes a ligand mediated co-factor interaction between purified bacterial expressed ligand binding domain of human LRH1 and a TIF2-deriv...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/29/2008
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50511471(CHEMBL4467442)
Affinity DataKi:  64nMAssay Description:Displacement of 6N-FAM from human LRH1 LBD (299 to 541 residues) expressed in Escherichia coli BL21 pLysS by competitive binding based fluorescence p...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM22382((3aS,6aR)-5-(hexan-2-yl)-N,4-diphenyl-1,2,3,3a,6,6...)
Affinity DataEC50:  70nMpH: 7.5 T: 2°CAssay Description:The screen utilizes a ligand mediated co-factor interaction between purified bacterial expressed ligand binding domain of human LRH1 and a TIF2-deriv...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/29/2008
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50467998(CHEMBL4288877)
Affinity DataKi:  81nMAssay Description:Displacement of 6N-FAM from human LRH1 LBD (299 to 541 residues) expressed in Escherichia coli BL21 pLysS by competitive binding based fluorescence p...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM22374((3aS,6aR)-4-methyl-5-[(4E)-oct-4-en-4-yl]-N-phenyl...)
Affinity DataEC50:  90nMpH: 7.5 T: 2°CAssay Description:The screen utilizes a ligand mediated co-factor interaction between purified bacterial expressed ligand binding domain of human LRH1 and a TIF2-deriv...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/29/2008
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50418312(CHEMBL1765932)
Affinity DataEC50:  100nMAssay Description:Agonist activity at human LRH-1 receptor assessed as TIF2 737-757 peptide recruitment by TR-FRET assay relative to controlMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM22378((3aS,6aR)-4-(3-methoxyphenyl)-5-[(4E)-oct-4-en-4-y...)
Affinity DataEC50:  100nMpH: 7.5 T: 2°CAssay Description:The screen utilizes a ligand mediated co-factor interaction between purified bacterial expressed ligand binding domain of human LRH1 and a TIF2-deriv...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/29/2008
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50505367(CHEMBL4565513)
Affinity DataEC50:  100nMAssay Description:Agonist activity at human full length LRH1 transfected in human HeLa cells incubated for 24 hrs by renilla luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/18/2021
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50511467(CHEMBL4551205)
Affinity DataEC50:  100nMAssay Description:Agonist activity at LRH-1 (unknown origin) transfected in human HeLa cells measured after 24 hrs by Dual Glo luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/25/2023
Entry Details
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50605641(CHEMBL5177743)
Affinity DataKd:  120nMAssay Description:Binding affinity to N-terminal 6-His tagged human LRH-1 LBD (299 to 541 residues) expressed in Escherichia coli BL21-(DE3) assessed as dissociation c...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/25/2023
Entry Details
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM95538([(Z)-[amino-(5-nitrofuran-2-yl)methylidene]amino] ...)
Affinity DataIC50: 143nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/21/2013
Entry Details
PCBioAssay
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM54414(MLS001204059 | N-(4-chloro-1,3-benzothiazol-2-yl)-...)
Affinity DataIC50: 148nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/21/2013
Entry Details
PCBioAssay
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM22388((3aS,6aR)-N,4,5-triphenyl-1,2,3,3a,6,6a-hexahydrop...)
Affinity DataEC50:  150nMpH: 7.5 T: 2°CAssay Description:The screen utilizes a ligand mediated co-factor interaction between purified bacterial expressed ligand binding domain of human LRH1 and a TIF2-deriv...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/29/2008
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50418306(CHEMBL1765955)
Affinity DataEC50:  158nMAssay Description:Agonist activity at human LRH-1 receptor assessed as TIF2 737-757 peptide recruitment by TR-FRET assay relative to controlMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM22377((3aS,6aR)-4-(4-bromophenyl)-5-[(4E)-oct-4-en-4-yl]...)
Affinity DataEC50:  160nMpH: 7.5 T: 2°CAssay Description:The screen utilizes a ligand mediated co-factor interaction between purified bacterial expressed ligand binding domain of human LRH1 and a TIF2-deriv...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/29/2008
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM95592(cid_8069390 | SMR000652760 | 2-(4,7-dimethyl-2-oxo...)
Affinity DataIC50: 168nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/21/2013
Entry Details
PCBioAssay
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM95632(MLS002163358 | cid_4789729 | N-(4-bromo-2-methylph...)
Affinity DataIC50: 169nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/21/2013
Entry Details
PCBioAssay
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM95539([(Z)-[amino-(5-nitrofuran-2-yl)methylidene]amino] ...)
Affinity DataIC50: 198nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/21/2013
Entry Details
PCBioAssay
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50418304(CHEMBL1765953)
Affinity DataEC50:  200nMAssay Description:Agonist activity at human LRH-1 receptor assessed as TIF2 737-757 peptide recruitment by TR-FRET assay relative to controlMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM22386((3aS,6aR)-5-cyclohexyl-N,4-diphenyl-1,2,3,3a,6,6a-...)
Affinity DataEC50:  230nMpH: 7.5 T: 2°CAssay Description:The screen utilizes a ligand mediated co-factor interaction between purified bacterial expressed ligand binding domain of human LRH1 and a TIF2-deriv...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/29/2008
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50418310(CHEMBL1765962)
Affinity DataEC50:  251nMAssay Description:Agonist activity at human LRH-1 receptor assessed as TIF2 737-757 peptide recruitment by TR-FRET assay relative to controlMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50418308(CHEMBL1765933)
Affinity DataEC50:  251nMAssay Description:Agonist activity at human LRH-1 receptor assessed as TIF2 737-757 peptide recruitment by TR-FRET assay relative to controlMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50418309(CHEMBL1765956)
Affinity DataEC50:  251nMAssay Description:Agonist activity at human LRH-1 receptor assessed as TIF2 737-757 peptide recruitment by TR-FRET assay relative to controlMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50418303(CHEMBL1765959)
Affinity DataEC50:  251nMAssay Description:Agonist activity at human LRH-1 receptor assessed as TIF2 737-757 peptide recruitment by TR-FRET assay relative to controlMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50418313(CHEMBL1765945)
Affinity DataEC50:  251nMAssay Description:Agonist activity at human LRH-1 receptor assessed as TIF2 737-757 peptide recruitment by TR-FRET assay relative to controlMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50544054(CHEMBL4638625)
Affinity DataKi:  280nMAssay Description:Displacement of 6N-FAM from human LRH1 LBD (299 to 541 residues) expressed in Escherichia coli BL21 pLysS by competitive binding based fluorescence p...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM95583(N-cyclopropyl-2-(4-ethyl-7-methyl-2-oxidanylidene-...)
Affinity DataIC50: 292nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/21/2013
Entry Details
PCBioAssay
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50418325(CHEMBL1765958)
Affinity DataEC50:  316nMAssay Description:Agonist activity at human LRH-1 receptor assessed as TIF2 737-757 peptide recruitment by TR-FRET assay relative to controlMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50418307(CHEMBL1765934)
Affinity DataEC50:  316nMAssay Description:Agonist activity at human LRH-1 receptor assessed as TIF2 737-757 peptide recruitment by TR-FRET assay relative to controlMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50511467(CHEMBL4551205)
Affinity DataKd:  320nMAssay Description:Binding affinity to N-terminal 6-His tagged human LRH-1 LBD (299 to 541 residues) expressed in Escherichia coli BL21-(DE3) assessed as dissociation c...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/25/2023
Entry Details
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM22383((3aS,6aR)-5-(decan-2-yl)-N,4-diphenyl-1,2,3,3a,6,6...)
Affinity DataEC50:  320nMpH: 7.5 T: 2°CAssay Description:The screen utilizes a ligand mediated co-factor interaction between purified bacterial expressed ligand binding domain of human LRH1 and a TIF2-deriv...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/29/2008
Entry Details Article
PubMed
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50417872(CHEMBL4303467)
Affinity DataIC50: 320nMAssay Description:Inhibition of full length LRH1 transfected in HEK293T cells incubated for 20 hrs by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/19/2024
Entry Details
PubMed
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