Compile Data Set for Download or QSAR
maximum 50k data
Found 40 with Last Name = 'villafranca' and Initial = 'j'
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50403490(CHEMBL312157)
Affinity DataKi:  2.80nMAssay Description:Inhibitory activity of compound against FK506 binding protein 12 was determinedMore data for this Ligand-Target Pair
In DepthDetails Article
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50403488(CHEMBL81439)
Affinity DataKi:  68nMAssay Description:Inhibitory activity of compound against FK506 binding protein 12 was determinedMore data for this Ligand-Target Pair
In DepthDetails Article
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50403487(CHEMBL82511)
Affinity DataKi:  81nMAssay Description:Inhibitory activity of compound against FK506 binding protein 12 was determinedMore data for this Ligand-Target Pair
In DepthDetails Article
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50403489(CHEMBL79747)
Affinity DataKi:  112nMAssay Description:Inhibitory activity of compound against FK506 binding protein 12 was determinedMore data for this Ligand-Target Pair
In DepthDetails Article
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50408099(CHEMBL57087)
Affinity DataKi:  120nMAssay Description:Apparent inhibition constant of Wild-type human recombinant FK506 binding protein 12More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50408102(CHEMBL55646)
Affinity DataKi:  150nMAssay Description:Apparent inhibition constant of Wild-type human recombinant FK506 binding protein 12More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50408104(CHEMBL292238)
Affinity DataKi:  200nMAssay Description:Apparent inhibition constant of Wild-type human recombinant FK506 binding protein 12More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288769((S)-1-[2-((1S,2R,5R)-1-Hydroxy-5-isopropyl-2-methy...)
Affinity DataKi:  210nMAssay Description:Inhibitory activity of compound against FK506 binding protein 12 was determinedMore data for this Ligand-Target Pair
In DepthDetails Article
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50408110(CHEMBL293284)
Affinity DataKi:  220nMAssay Description:Apparent inhibition constant of Wild-type human recombinant FK506 binding protein 12More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50403486(CHEMBL82427)
Affinity DataKi:  258nMAssay Description:Inhibitory activity of compound against FK506 binding protein 12 was determinedMore data for this Ligand-Target Pair
In DepthDetails Article
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288762((1S,10R)-14-[2-Oxo-2-(3,4,5-trimethoxy-phenyl)-ace...)
Affinity DataKi:  280nMAssay Description:Compound was evaluated for inhibitory activity against human FKBP-12 rotamaseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50408096(CHEMBL301025)
Affinity DataKi:  350nMAssay Description:Apparent inhibition constant of Wild-type human recombinant FK506 binding protein 12More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50408101(CHEMBL293519)
Affinity DataKi:  370nMAssay Description:Apparent inhibition constant of Wild-type human recombinant FK506 binding protein 12More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50408094(CHEMBL59256)
Affinity DataKi:  390nMAssay Description:Apparent inhibition constant of Wild-type human recombinant FK506 binding protein 12More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50408105(CHEMBL294146)
Affinity DataKi:  550nMAssay Description:Apparent inhibition constant of Wild-type human recombinant FK506 binding protein 12More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50408100(CHEMBL57674)
Affinity DataKi:  570nMAssay Description:Apparent inhibition constant of Wild-type human recombinant FK506 binding protein 12More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50408103(CHEMBL293294)
Affinity DataKi:  790nMAssay Description:Apparent inhibition constant of Wild-type human recombinant FK506 binding protein 12More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288763((1S,9R)-5-Benzyloxymethyl-13-[2-oxo-2-(3,4,5-trime...)
Affinity DataKi:  1.20E+3nMAssay Description:Compound was evaluated for inhibitory activity against human FKBP-12 rotamaseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288765((1S,9R)-5-(tert-Butyl-dimethyl-silanyloxymethyl)-1...)
Affinity DataKi:  1.50E+3nMAssay Description:Compound was evaluated for inhibitory activity against human FKBP-12 rotamaseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetDopamine beta-hydroxylase(Bos taurus)
Pennsylvania State University

Curated by ChEMBL
LigandPNGBDBM50017831(2-[1,3]Dithiolan-2-ylidene-ethylamine | CHEMBL1635...)
Affinity DataKi:  5.00E+3nMAssay Description:Compound was evaluated for the ability to bind to dopamine beta-hydroxylase of bovineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50408107(CHEMBL56789)
Affinity DataKi:  6.50E+3nMAssay Description:Apparent inhibition constant of Wild-type human recombinant FK506 binding protein 12More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50408097(CHEMBL56270)
Affinity DataKi:  7.20E+3nMAssay Description:Apparent inhibition constant of Wild-type human recombinant FK506 binding protein 12More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288764((1S,9R)-13-[2-((1S,2R,5R)-1-Hydroxy-5-isopropyl-2-...)
Affinity DataKi:  8.10E+3nMAssay Description:Compound was evaluated for inhibitory activity against human FKBP-12 rotamaseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288768((1R,10S)-14-(3,3-Dimethyl-2-oxo-pentanoyl)-3,8-dio...)
Affinity DataKi:  8.30E+3nMAssay Description:Compound was evaluated for inhibitory activity against human FKBP-12 rotamaseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50408109(CHEMBL54055)
Affinity DataKi:  8.40E+3nMAssay Description:Apparent inhibition constant of Wild-type human recombinant FK506 binding protein 12More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288767((1R,9S)-13-(3,3-Dimethyl-2-oxo-pentanoyl)-3,7-diox...)
Affinity DataKi:  1.00E+4nMAssay Description:Compound was evaluated for inhibitory activity against human FKBP-12 rotamaseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50408106(CHEMBL56927)
Affinity DataKi:  1.40E+4nMAssay Description:Apparent inhibition constant of Wild-type human recombinant FK506 binding protein 12More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50408098(CHEMBL298828)
Affinity DataKi:  2.40E+4nMAssay Description:Apparent inhibition constant of Wild-type human recombinant FK506 binding protein 12More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDopamine beta-hydroxylase(Bos taurus)
Pennsylvania State University

Curated by ChEMBL
LigandPNGBDBM50017830(Benzofuran-6-ol | CHEMBL351630)
Affinity DataKi:  4.00E+4nMAssay Description:Compound was evaluated for the ability to bind to dopamine beta-hydroxylase of bovineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288766((1S,9R)-13-{2-[(1S,2R,5R)-1-Hydroxy-5-(2-methoxy-1...)
Affinity DataKi: >5.00E+4nMAssay Description:Compound was evaluated for inhibitory activity against human FKBP-12 rotamaseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetDopamine beta-hydroxylase(Bos taurus)
Pennsylvania State University

Curated by ChEMBL
LigandPNGBDBM50017834(4-(1-Aminomethyl-prop-2-ynyl)-phenol | CHEMBL16312...)
Affinity DataKi:  5.70E+4nMAssay Description:Compound was evaluated for the ability to bind to dopamine beta-hydroxylase of bovineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50408095(CHEMBL292166)
Affinity DataKi:  6.70E+4nMAssay Description:Apparent inhibition constant of Wild-type human recombinant FK506 binding protein 12More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50408108(CHEMBL299276)
Affinity DataKi:  8.30E+4nMAssay Description:Apparent inhibition constant of Wild-type human recombinant FK506 binding protein 12More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288769((S)-1-[2-((1S,2R,5R)-1-Hydroxy-5-isopropyl-2-methy...)
Affinity DataKi:  2.10E+5nMAssay Description:Compound was evaluated for inhibitory activity against human FKBP-12 rotamaseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetDopamine beta-hydroxylase(Bos taurus)
Pennsylvania State University

Curated by ChEMBL
LigandPNGBDBM50017827(4-(1-Aminomethyl-vinyl)-phenol | CHEMBL330118)
Affinity DataKi:  5.20E+5nMAssay Description:Compound was evaluated for the ability to bind to dopamine beta-hydroxylase of bovineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDopamine beta-hydroxylase(Bos taurus)
Pennsylvania State University

Curated by ChEMBL
LigandPNGBDBM50017833(4-Hydroxystyrene | 4-Vinylphenol | 4-ethenylphenol...)
Affinity DataKi:  7.00E+5nMAssay Description:Compound was evaluated for the ability to bind to dopamine beta-hydroxylase of bovineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDopamine beta-hydroxylase(Bos taurus)
Pennsylvania State University

Curated by ChEMBL
LigandPNGBDBM50017829(Benzofuran-5-ol | CHEMBL349283)
Affinity DataKi:  1.90E+6nMAssay Description:Compound was evaluated for the ability to bind to dopamine beta-hydroxylase of bovineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDopamine beta-hydroxylase(Bos taurus)
Pennsylvania State University

Curated by ChEMBL
LigandPNGBDBM50017828(Benzofuran-7-ol | CHEMBL351411)
Affinity DataKi:  3.20E+6nMAssay Description:Compound was evaluated for the ability to bind to dopamine beta-hydroxylase of bovineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDopamine beta-hydroxylase(Bos taurus)
Pennsylvania State University

Curated by ChEMBL
LigandPNGBDBM50017832(4-Propenyl-phenol | CHEMBL163297)
Affinity DataKi: >2.00E+7nMAssay Description:Compound was evaluated for the ability to bind to dopamine beta-hydroxylase of bovineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbamoyl-phosphate synthase small chain(Escherichia coli (strain K12))
Pennsylvania State University

LigandPNGBDBM100279(Etheno-AMP | US11185100, TABLE 7.4 | [(2R,3S,4R,5R...)
Affinity DataKd:  3.30E+4nMpH: 7.5 T: 2°CMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed