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TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bologna

LigandPNGBDBM9914(3-[(R)-1H-imidazol-1-yl(4-nitrophenyl)methyl]-4H-c...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/13/2006
Entry Details Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bologna

LigandPNGBDBM9915(3-[(S)-1H-imidazol-1-yl(4-nitrophenyl)methyl]-4H-c...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/13/2006
Entry Details Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bologna

LigandPNGBDBM9916(CHEMBL522917 | 3-[(R)-(4-bromophenyl)(1H-imidazol-...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/13/2006
Entry Details Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bologna

LigandPNGBDBM9917(3-[(S)-(4-bromophenyl)(1H-imidazol-1-yl)methyl]-4H...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/13/2006
Entry Details Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bologna

LigandPNGBDBM9918(CHEMBL225079 | 4-[(R)-1H-imidazol-1-yl(4-oxo-4H-ch...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/13/2006
Entry Details Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bologna

LigandPNGBDBM9919(CHEMBL451201 | 4-[(S)-1H-imidazol-1-yl(4-oxo-4H-ch...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/13/2006
Entry Details Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
University of Bologna

LigandPNGBDBM9920(CHEMBL31215 | 4-[(5S)-5H,6H,7H,8H-imidazo[1,5-a]py...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/13/2006
Entry Details Article
PubMed
TargetPolycomb protein EED(Human)
Novartis Institutes For Biomedical Research

LigandPNGBDBM225230(EED226 | US11013745, Compound EED226)
Affinity DataKd:  82nMpH: 8.0 T: 2°CAssay Description:ITC experiments were performed by Auto ITC200 (Microcal) at 25 °C. ITC sample cell was filled with 10 μM PRC2 in titration buffer (25 mM HEPES p...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/9/2017
Entry Details Article
PubMed
LigandPNGBDBM225230(EED226 | US11013745, Compound EED226)
Affinity DataKd:  114nMpH: 8.0 T: 2°CAssay Description:ITC experiments were performed by Auto ITC200 (Microcal) at 25 °C. ITC sample cell was filled with 10 μM PRC2 in titration buffer (25 mM HEPES p...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/9/2017
Entry Details Article
PubMed
TargetGrowth hormone secretagogue receptor type 1(Rat)
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50066812((E)-5-Amino-5-methyl-hex-2-enoic acid ((R)-1-{[(R)...)
Affinity DataEC50:  8.90nMAssay Description:Tested for GH-releasing property using classical rat pituitary cell assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGrowth hormone secretagogue receptor type 1(Rat)
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50066809((E)-5-Amino-5-methyl-hex-2-enoic acid {(R)-2-benzo...)
Affinity DataEC50:  35nMAssay Description:Tested for GH-releasing property using classical rat pituitary cell assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGrowth hormone secretagogue receptor type 1(Rat)
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50066810((E)-5-Amino-5-methyl-hex-2-enoic acid {(R)-1-[((R)...)
Affinity DataEC50:  13nMAssay Description:Tested for GH-releasing property using classical rat pituitary cell assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGrowth hormone secretagogue receptor type 1(Rat)
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50066811((E)-5-Amino-5-methyl-hex-2-enoic acid {(R)-2-benzy...)
Affinity DataEC50:  5nMAssay Description:Tested for GH-releasing property using classical rat pituitary cell assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGrowth hormone secretagogue receptor type 1(Rat)
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50066812((E)-5-Amino-5-methyl-hex-2-enoic acid ((R)-1-{[(R)...)
Affinity DataEC50:  8.90nMAssay Description:Tested for GH-releasing property using classical rat pituitary cell assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGrowth hormone secretagogue receptor type 1(Rat)
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50066814((E)-5-Amino-5-methyl-hex-2-enoic acid [(R)-1-{[(R)...)
Affinity DataEC50:  6nMAssay Description:Tested for GH-releasing property using classical rat pituitary cell assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGrowth hormone secretagogue receptor type 1(Rat)
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50066813((E)-5-Amino-5-methyl-hex-2-enoic acid ((R)-1-{[(R)...)
Affinity DataEC50:  45nMAssay Description:Tested for GH-releasing property using classical rat pituitary cell assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGrowth hormone secretagogue receptor type 1(Rat)
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50066819((E)-5-Amino-5-methyl-hex-2-enoic acid {(R)-2-biphe...)
Affinity DataEC50:  3nMAssay Description:Tested for GH-releasing property using classical rat pituitary cell assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGrowth hormone secretagogue receptor type 1(Rat)
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50066816((E)-5-Amino-5-methyl-hex-2-enoic acid methyl-{(R)-...)
Affinity DataEC50:  18nMAssay Description:Tested for GH-releasing property using classical rat pituitary cell assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGrowth hormone secretagogue receptor type 1(Rat)
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50066817((E)-5-Amino-5-methyl-hex-2-enoic acid ((R)-1-{[(R)...)
Affinity DataEC50:  5nMAssay Description:Tested for GH-releasing property using classical rat pituitary cell assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGrowth hormone secretagogue receptor type 1(Rat)
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50066818((E)-5-Amino-5-methyl-hex-2-enoic acid methyl-[(R)-...)
Affinity DataEC50:  21nMAssay Description:Tested for GH-releasing property using classical rat pituitary cell assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGrowth hormone secretagogue receptor type 1(Rat)
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50066820((E)-5-Amino-5-methyl-hex-2-enoic acid ((R)-1-{[(R)...)
Affinity DataEC50:  20nMAssay Description:Tested for GH-releasing property using classical rat pituitary cell assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGrowth hormone secretagogue receptor type 1(Rat)
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50066823((E)-5-Amino-5-methyl-hex-2-enoic acid ((R)-1-{[(R)...)
Affinity DataEC50:  17nMAssay Description:Tested for GH-releasing property using classical rat pituitary cell assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGrowth hormone secretagogue receptor type 1(Rat)
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50066822((E)-5-Amino-5-methyl-hex-2-enoic acid methyl-[(R)-...)
Affinity DataEC50:  16nMAssay Description:Tested for GH-releasing property using classical rat pituitary cell assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGrowth hormone secretagogue receptor type 1(Rat)
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50066821((E)-5-Amino-5-methyl-hex-2-enoic acid ((R)-1-{[(R)...)
Affinity DataEC50:  8nMAssay Description:Tested for GH-releasing property using classical rat pituitary cell assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGrowth hormone secretagogue receptor type 1(Rat)
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50066824((E)-5-Amino-5-methyl-hex-2-enoic acid methyl-{(R)-...)
Affinity DataEC50:  24nMAssay Description:Tested for GH-releasing property using classical rat pituitary cell assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGrowth hormone secretagogue receptor type 1(Rat)
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50066825((E)-5-Amino-5-methyl-hex-2-enoic acid [(R)-1-{[(R)...)
Affinity DataEC50:  1.5nMAssay Description:Tested for GH-releasing property using classical rat pituitary cell assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGrowth hormone secretagogue receptor type 1(Rat)
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50066826((E)-5-Amino-5-methyl-hex-2-enoic acid ((R)-1-{[(R)...)
Affinity DataEC50:  1.80nMAssay Description:Tested for GH-releasing property using classical rat pituitary cell assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGrowth hormone secretagogue receptor type 1(Rat)
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50066827((E)-5-Amino-5-methyl-hex-2-enoic acid methyl-{(R)-...)
Affinity DataEC50:  2nMAssay Description:Tested for GH-releasing property using classical rat pituitary cell assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVitamin D3 receptor(Human)
Tokyo Medical and Dental University

Curated by ChEMBL
LigandPNGBDBM50198705(CHEMBL226435 | (2Z)-(20R)-1alpha,25-dihydroxy-2-[(...)
Affinity DataEC50:  2.20nMAssay Description:Inhibition of human VDR induced-transcriptional transactivation of luciferase reporter gene in COS7 cells after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVitamin D3 receptor(Human)
Tokyo Medical and Dental University

Curated by ChEMBL
LigandPNGBDBM50198705(CHEMBL226435 | (2Z)-(20R)-1alpha,25-dihydroxy-2-[(...)
Affinity DataEC50:  0.5nMAssay Description:Inhibition of human VDR induced-transcriptional transactivation of luciferase reporter gene in COS7 cells after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVitamin D3 receptor(Human)
Tokyo Medical and Dental University

Curated by ChEMBL
LigandPNGBDBM50198707((2Z)-(20S)-1alpha,25-dihydroxy-2-[2''''-(fluoroeth...)
Affinity DataEC50:  1.10nMAssay Description:Inhibition of human VDR induced-transcriptional transactivation of luciferase reporter gene in COS7 cells after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVitamin D3 receptor(Human)
Tokyo Medical and Dental University

Curated by ChEMBL
LigandPNGBDBM50198707((2Z)-(20S)-1alpha,25-dihydroxy-2-[2''''-(fluoroeth...)
Affinity DataEC50:  0.0700nMAssay Description:Inhibition of human VDR induced-transcriptional transactivation of luciferase reporter gene in COS7 cells after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVitamin D3 receptor(Mouse)
Tokyo Medical and Dental University

Curated by ChEMBL
LigandPNGBDBM50244240((20S)-(2E)-1-alpha-25-Dihydroxy-2-[2-(hydroxy)-eth...)
Affinity DataEC50:  0.0260nMAssay Description:Increase in mouse VDR-mediated transcriptional activity in african green monkey COS7 cells after 24 hrs by luciferase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetVitamin D3 receptor(Mouse)
Tokyo Medical and Dental University

Curated by ChEMBL
LigandPNGBDBM50412385(CHEMBL2021488)
Affinity DataEC50:  0.0900nMAssay Description:Increase in mouse VDR-mediated transcriptional activity in african green monkey COS7 cells after 24 hrs by luciferase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetVitamin D3 receptor(Mouse)
Tokyo Medical and Dental University

Curated by ChEMBL
LigandPNGBDBM50005618(CHEMBL2021484)
Affinity DataEC50:  0.00210nMAssay Description:Increase in mouse VDR-mediated transcriptional activity in african green monkey COS7 cells after 24 hrs by luciferase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetVitamin D3 receptor(Mouse)
Tokyo Medical and Dental University

Curated by ChEMBL
LigandPNGBDBM50244241((20R)-(2E)-1-alpha-25-Dihydroxy-2-[2-(hydroxy)-eth...)
Affinity DataEC50:  0.200nMAssay Description:Increase in mouse VDR-mediated transcriptional activity in african green monkey COS7 cells after 24 hrs by luciferase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetVitamin D3 receptor(Mouse)
Tokyo Medical and Dental University

Curated by ChEMBL
LigandPNGBDBM50244165(CHEMBL514116 | (20R)-1-alpha,25-Dihydroxy-2-alpha-...)
Affinity DataEC50:  0.0240nMAssay Description:Increase in mouse VDR-mediated transcriptional activity in african green monkey COS7 cells after 24 hrs by luciferase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetVitamin D3 receptor(Mouse)
Tokyo Medical and Dental University

Curated by ChEMBL
LigandPNGBDBM50244269(CHEMBL513573 | (20R)-1-alpha-2-alpha-25-Trihydroxy...)
Affinity DataEC50:  0.120nMAssay Description:Increase in mouse VDR-mediated transcriptional activity in african green monkey COS7 cells after 24 hrs by luciferase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetVitamin D3 receptor(Mouse)
Tokyo Medical and Dental University

Curated by ChEMBL
LigandPNGBDBM50412386(CHEMBL2021486)
Affinity DataEC50:  0.0580nMAssay Description:Increase in mouse VDR-mediated transcriptional activity in african green monkey COS7 cells after 24 hrs by luciferase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetVitamin D3 receptor(Mouse)
Tokyo Medical and Dental University

Curated by ChEMBL
LigandPNGBDBM50244241((20R)-(2E)-1-alpha-25-Dihydroxy-2-[2-(hydroxy)-eth...)
Affinity DataEC50:  0.0290nMAssay Description:Increase in mouse VDR-mediated transcriptional activity in african green monkey COS7 cells after 24 hrs by luciferase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetVitamin D3 receptor(Mouse)
Tokyo Medical and Dental University

Curated by ChEMBL
LigandPNGBDBM50244165(CHEMBL514116 | (20R)-1-alpha,25-Dihydroxy-2-alpha-...)
Affinity DataEC50:  0.115nMAssay Description:Increase in mouse VDR-mediated transcriptional activity in african green monkey COS7 cells after 24 hrs by luciferase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetVitamin D3 receptor(Mouse)
Tokyo Medical and Dental University

Curated by ChEMBL
LigandPNGBDBM50244268((20S)-1-alpha-2-alpha-25-Trihydroxy-2beta-methyl-1...)
Affinity DataEC50:  1.90nMAssay Description:Increase in mouse VDR-mediated transcriptional activity in african green monkey COS7 cells after 24 hrs by luciferase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetVitamin D3 receptor(Mouse)
Tokyo Medical and Dental University

Curated by ChEMBL
LigandPNGBDBM50244269(CHEMBL513573 | (20R)-1-alpha-2-alpha-25-Trihydroxy...)
Affinity DataEC50:  4.5nMAssay Description:Increase in mouse VDR-mediated transcriptional activity in african green monkey COS7 cells after 24 hrs by luciferase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetVitamin D3 receptor(Human)
Tokyo Medical and Dental University

Curated by ChEMBL
LigandPNGBDBM50292704((25R)-26-adamantyl-1R,25-hydroxy-2-methylene-22,23...)
Affinity DataEC50:  24nMAssay Description:Agonist activity at VDR assessed as receptor transactivation by transient transcription assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetVitamin D3 receptor(Human)
Tokyo Medical and Dental University

Curated by ChEMBL
LigandPNGBDBM50292705((25R)-25-Adamantyl-1alpha,25-dihydroxy-2-methylene...)
Affinity DataEC50:  1nMAssay Description:Agonist activity at VDR assessed as receptor transactivation by transient transcription assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetVitamin D3 receptor(Human)
Tokyo Medical and Dental University

Curated by ChEMBL
LigandPNGBDBM50292706((24R)-24-Adamantyl-1r,24-dihydroxy-2-methylene-22,...)
Affinity DataEC50:  0.0200nMAssay Description:Agonist activity at VDR assessed as receptor transactivation by transient transcription assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetVitamin D3 receptor(Rat)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50200182((1S,3R,5Z,7E)-9,10-secocholesta-5,7,10(19)-triene-...)
Affinity DataEC50:  0.200nMAssay Description:Activity at rat recombinant full length VDR expressed in rat ROS 17/2.8 cells transfected with 24-hydroxylase gene promoter assessed as transcription...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetVitamin D3 receptor(Rat)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50292630((5R)-5-{(2R)-2-[(1R,3R,7E)-1,3-Dihydroxy-2-methyle...)
Affinity DataEC50:  100nMAssay Description:Activity at rat recombinant full length VDR expressed in rat ROS 17/2.8 cells transfected with 24-hydroxylase gene promoter assessed as transcription...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetVitamin D3 receptor(Rat)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50292629((23S)-25-dehydro-2-methylene-19-nor-1alpha-hydroxy...)
Affinity DataEC50:  2nMAssay Description:Activity at rat recombinant full length VDR expressed in rat ROS 17/2.8 cells transfected with 24-hydroxylase gene promoter assessed as transcription...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetVitamin D3 receptor(Rat)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50200182((1S,3R,5Z,7E)-9,10-secocholesta-5,7,10(19)-triene-...)
Affinity DataEC50:  0.200nMAssay Description:Activity at VDR in rat ROS 17/2.8 cells assessed as transcriptional activation of 24-hydroxylase gene promoter after 16 hrs by luciferase reporter ge...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
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