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Found 39 with Last Name = 'wakselman' and Initial = 'm'
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50064657(CHEMBL277390 | Cyclo(Lys(alphaH2+)-Pro-Aba-[CH2SMe...)
Affinity DataKi:  85nMAssay Description:Inhibitory activity against hydrolysis of Gly-Pro-pNa by CD26 (dipeptidylpeptidase 4) purified from CEM H01 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50064657(CHEMBL277390 | Cyclo(Lys(alphaH2+)-Pro-Aba-[CH2SMe...)
Affinity DataKi:  470nMAssay Description:Inhibitory kinetic constant against Dipeptidyl peptidase IV purified from CD26-negative C8166 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Cnrs-Cercoa

Curated by ChEMBL
LigandPNGBDBM50021959(CHEMBL777 | MM 14151 | US9120808, Clavulanic acid ...)
Affinity DataKi:  800nMAssay Description:Inhibition constant (Ki) for TEM-1 beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Cnrs-Cercoa

Curated by ChEMBL
LigandPNGBDBM50021954((2S,5R)-3,3-Dimethyl-4,4,7-trioxo-4lambda*6*-thia-...)
Affinity DataKi:  800nMAssay Description:Inhibition constant (Ki) for TEM-1 beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Cnrs-Cercoa

Curated by ChEMBL
LigandPNGBDBM50022785(4-Methyl-3-(2-oxo-azetidin-1-yl)-benzoic acid | CH...)
Affinity DataKi:  1.00E+4nMAssay Description:Inhibition constant (Ki) for TEM-1 beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Bos taurus (bovine))
Cnrs-Cercoa

Curated by ChEMBL
LigandPNGBDBM50368614(CHEMBL540392)
Affinity DataKi:  1.20E+4nMAssay Description:Apparent binding constant against bovine trypsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Cnrs-Cercoa

Curated by ChEMBL
LigandPNGBDBM50022788((2S,5R,6R)-6-(3-(2-chlorophenyl)-5-methylisoxazole...)
Affinity DataKi:  1.30E+4nMAssay Description:Inhibition constant (Ki) for TEM-1 beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Cnrs-Cercoa

Curated by ChEMBL
LigandPNGBDBM50022787((+)-3,3-Dimethyl-7-oxo-6-phenylacetylamino-4-thia-...)
Affinity DataKi:  2.00E+4nMAssay Description:Inhibition constant (Ki) for TEM-1 beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Cnrs-Cercoa

Curated by ChEMBL
LigandPNGBDBM50022786(3-(3-Fluoro-2-oxo-azetidin-1-yl)-4-methyl-benzoic ...)
Affinity DataKi:  2.00E+4nMAssay Description:Inhibition constant (Ki) for TEM-1 beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAnionic trypsin(Bos taurus)
Cnrs-Cercoa

Curated by ChEMBL
LigandPNGBDBM50047473(CHEMBL38512 | N-[3-(11-Bromomethyl-3,6,9-trioxo-2,...)
Affinity DataKi:  2.00E+4nMAssay Description:Apparent binding constant against porcine trypsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Cnrs-Cercoa

Curated by ChEMBL
LigandPNGBDBM50022790(1-Oxo-2,2a,3,4-tetrahydro-1H-azeto[1,2-a]quinoline...)
Affinity DataKi:  2.00E+4nMAssay Description:Inhibition constant (Ki) for TEM-1 beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Cnrs-Cercoa

Curated by ChEMBL
LigandPNGBDBM50022789(4-Fluoro-1-oxo-2,2a,3,4-tetrahydro-1H-azeto[1,2-a]...)
Affinity DataKi:  3.90E+4nMAssay Description:Inhibition constant (Ki) for TEM-1 beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Cnrs-Cercoa

Curated by ChEMBL
LigandPNGBDBM50022794(3-(3-Bromo-2-oxo-azetidin-1-yl)-4-methyl-benzoic a...)
Affinity DataKi:  4.00E+4nMAssay Description:Inhibition constant (Ki) for TEM-1 beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Cnrs-Cercoa

Curated by ChEMBL
LigandPNGBDBM50368615(CHEMBL553244)
Affinity DataKi:  4.10E+4nMAssay Description:Apparent binding constant against Human urokinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Cnrs-Cercoa

Curated by ChEMBL
LigandPNGBDBM50022792(4-Chloro-1-oxo-2,2a,3,4-tetrahydro-1H-azeto[1,2-a]...)
Affinity DataKi:  5.00E+4nMAssay Description:Inhibition constant (Ki) for TEM-1 beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Bos taurus (bovine))
Cnrs-Cercoa

Curated by ChEMBL
LigandPNGBDBM50047473(CHEMBL38512 | N-[3-(11-Bromomethyl-3,6,9-trioxo-2,...)
Affinity DataKi:  5.50E+4nMAssay Description:Apparent binding constant against bovine trypsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Cnrs-Cercoa

Curated by ChEMBL
LigandPNGBDBM50022795(3-(3-Bromo-3-fluoro-2-oxo-azetidin-1-yl)-4-methyl-...)
Affinity DataKi:  6.00E+4nMAssay Description:Inhibition constant (Ki) for TEM-1 beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Bos taurus (bovine))
Cnrs-Cercoa

Curated by ChEMBL
LigandPNGBDBM50047476(4-(4-Amino-butyl)-11-bromomethyl-2,5,8-triaza-bicy...)
Affinity DataKi:  8.00E+4nMAssay Description:Apparent binding constant against bovine trypsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Cnrs-Cercoa

Curated by ChEMBL
LigandPNGBDBM50022793(3-(3,3-Difluoro-2-oxo-azetidin-1-yl)-4-methyl-benz...)
Affinity DataKi:  8.30E+4nMAssay Description:Inhibition constant (Ki) for TEM-1 beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Bos taurus (bovine))
Cnrs-Cercoa

Curated by ChEMBL
LigandPNGBDBM50368613(CHEMBL557221)
Affinity DataKi:  8.70E+4nMAssay Description:Apparent binding constant against bovine trypsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Cnrs-Cercoa

Curated by ChEMBL
LigandPNGBDBM50368614(CHEMBL540392)
Affinity DataKi:  9.00E+4nMAssay Description:Apparent binding constant against Human urokinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Cnrs-Cercoa

Curated by ChEMBL
LigandPNGBDBM50047473(CHEMBL38512 | N-[3-(11-Bromomethyl-3,6,9-trioxo-2,...)
Affinity DataKi:  9.20E+4nMAssay Description:Apparent binding constant against Human urokinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Cnrs-Cercoa

Curated by ChEMBL
LigandPNGBDBM50022791(3-(3,3-Dibromo-2-oxo-azetidin-1-yl)-4-methyl-benzo...)
Affinity DataKi:  1.60E+5nMAssay Description:Inhibition constant (Ki) for TEM-1 beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Cnrs-Cercoa

Curated by ChEMBL
LigandPNGBDBM50368613(CHEMBL557221)
Affinity DataKi:  5.00E+5nMAssay Description:Apparent binding constant against Human urokinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandPNGBDBM50014144(CHEMBL83462 | {(S)-1-[(1S,2R,3R,4S)-1-Benzyl-4-((R...)
Affinity DataIC50: <1nMAssay Description:Inhibitory concentration against HIV-1 proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandPNGBDBM50014147(A-74704 | CHEMBL430891 | {(S)-1-[(1S,3S)-1-Benzyl-...)
Affinity DataIC50:  3nMAssay Description:Inhibitory concentration against HIV-1 proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50064660(CHEMBL302602 | Cyclo(Lys(alphaH2+)-Pro-Aba-[CH2SMe...)
Affinity DataIC50:  3nMAssay Description:Inhibitory activity against hydrolysis of Gly-Pro-pNa by CD26 (Dipeptidyl peptidase IV) purified from CEM H01 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandPNGBDBM50282083((S)-2-((S)-2-{(2R,6R)-2-Benzyl-4-hydroxy-6-[(S)-1-...)
Affinity DataIC50:  5nMAssay Description:Concentration required for inhibitory activity against HIV-1 proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50064657(CHEMBL277390 | Cyclo(Lys(alphaH2+)-Pro-Aba-[CH2SMe...)
Affinity DataIC50:  12nMAssay Description:Inhibitory activity against hydrolysis of Gly-Pro-pNa by CD26 (Dipeptidyl peptidase IV) purified from CEM H01 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50064661(CHEMBL67679 | Cyclo(Lys(alphaH2+)-Pro-Aba-[CH2SBu2...)
Affinity DataIC50:  20nMAssay Description:Inhibitory activity against hydrolysis of Gly-Pro-pNa by CD26 (Dipeptidyl peptidase IV) purified from CEM H01 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50064656(CHEMBL67680 | Cyclo(Lys(alphaH2+)-Pro-Aba-[CH2SOct...)
Affinity DataIC50:  30nMAssay Description:Inhibitory activity against hydrolysis of Gly-Pro-pNa by CD26 (Dipeptidyl peptidase IV) purified from CEM H01 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50064661(CHEMBL67679 | Cyclo(Lys(alphaH2+)-Pro-Aba-[CH2SBu2...)
Affinity DataIC50:  570nMAssay Description:Inhibitory activity against hydrolysis of Gly-Pro-pNa by Dipeptidyl peptidase IV purified from CD26-negative C8166 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50064660(CHEMBL302602 | Cyclo(Lys(alphaH2+)-Pro-Aba-[CH2SMe...)
Affinity DataIC50:  610nMAssay Description:Inhibitory activity against hydrolysis of Gly-Pro-pNa by Dipeptidyl peptidase IV purified from CD26-negative C8166 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50064656(CHEMBL67680 | Cyclo(Lys(alphaH2+)-Pro-Aba-[CH2SOct...)
Affinity DataIC50:  630nMAssay Description:Inhibitory activity against hydrolysis of Gly-Pro-pNa by Dipeptidyl peptidase IV purified from CD26-negative C8166 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50064657(CHEMBL277390 | Cyclo(Lys(alphaH2+)-Pro-Aba-[CH2SMe...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibitory activity against hydrolysis of Gly-Pro-pNa by Dipeptidyl peptidase IV purified from CD26-negative C8166 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50064658(Cyclo(Lys(alphaH2+)-Pro-Aba-[CH2OAc]-Gly2-), CF3CO...)
Affinity DataIC50:  1.50E+3nMAssay Description:Inhibitory activity against hydrolysis of Gly-Pro-pNa by CD26 (Dipeptidyl peptidase IV) purified from CEM H01 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50064658(Cyclo(Lys(alphaH2+)-Pro-Aba-[CH2OAc]-Gly2-), CF3CO...)
Affinity DataIC50:  3.50E+3nMAssay Description:Inhibitory activity against hydrolysis of Gly-Pro-pNa by Dipeptidyl peptidase IV purified from CD26-negative C8166 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50064659((4S,10S)-10-Amino-24-phenoxymethyl-2,8,15,18,21-pe...)
Affinity DataIC50:  1.00E+4nMAssay Description:Inhibitory activity against hydrolysis of Gly-Pro-pNa by CD26 (Dipeptidyl peptidase IV) purified from CEM H01 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50064659((4S,10S)-10-Amino-24-phenoxymethyl-2,8,15,18,21-pe...)
Affinity DataIC50:  2.50E+4nMAssay Description:Inhibitory activity against hydrolysis of Gly-Pro-pNa by Dipeptidyl peptidase IV purified from CD26-negative C8166 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed