Compile Data Set for Download or QSAR
Report error Found 33 of ic50 data for polymerid = 4430,49000709
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148534(2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...)
Affinity DataIC50: 5nMAssay Description:Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancerMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148543(2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...)
Affinity DataIC50: 6nMAssay Description:Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancerMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148531(CHEMBL326292 | CHEMBL334279 | 2-[(1-Amino-2-cycloh...)
Affinity DataIC50: 8nMAssay Description:Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancerMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148532(CHEMBL420537 | CHEMBL333841 | 2-[(1-Amino-2-cycloh...)
Affinity DataIC50: 10nMAssay Description:Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancerMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148534(2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...)
Affinity DataIC50: 15nMAssay Description:Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancerMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148533(CHEMBL119118 | CHEMBL332970 | 2-[(1-Amino-2-cycloh...)
Affinity DataIC50: 20nMAssay Description:Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancerMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148531(CHEMBL326292 | CHEMBL334279 | 2-[(1-Amino-2-cycloh...)
Affinity DataIC50: 25nMAssay Description:Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancerMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148543(2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...)
Affinity DataIC50: 30nMAssay Description:Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancerMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148530(CHEMBL119392 | CHEMBL334143 | 2-[(1-Amino-2-cycloh...)
Affinity DataIC50: 30nMAssay Description:Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancerMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148528(CHEMBL332290 | 2-[(1-Amino-2-cyclohexyl-ethyl)-hyd...)
Affinity DataIC50: 40nMAssay Description:Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancerMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148541(2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...)
Affinity DataIC50: 45nMAssay Description:Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancerMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148536(2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...)
Affinity DataIC50: 70nMAssay Description:Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancerMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148529(2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...)
Affinity DataIC50: 100nMAssay Description:Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancerMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148529(2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...)
Affinity DataIC50: 100nMAssay Description:Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancerMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148536(2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...)
Affinity DataIC50: 150nMAssay Description:Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancerMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148533(CHEMBL119118 | CHEMBL332970 | 2-[(1-Amino-2-cycloh...)
Affinity DataIC50: 200nMAssay Description:Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancerMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148532(CHEMBL420537 | CHEMBL333841 | 2-[(1-Amino-2-cycloh...)
Affinity DataIC50: 200nMAssay Description:Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancerMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148541(2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...)
Affinity DataIC50: 250nMAssay Description:Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancerMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148530(CHEMBL119392 | CHEMBL334143 | 2-[(1-Amino-2-cycloh...)
Affinity DataIC50: 350nMAssay Description:Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancerMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148528(CHEMBL332290 | 2-[(1-Amino-2-cyclohexyl-ethyl)-hyd...)
Affinity DataIC50: 3.00E+3nMAssay Description:Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancerMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM36644(L-159,906)
Affinity DataIC50: 1.00E+5nMpH: 7.0 T: 2°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using dehydropeptidase 1 (DPH-1).More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM36642(L-809,370)
Affinity DataIC50: 1.00E+5nMpH: 7.0 T: 2°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using dehydropeptidase 1 (DPH-1).More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM36641(L-809,339)
Affinity DataIC50: 1.00E+5nMpH: 7.0 T: 2°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using dehydropeptidase 1 (DPH-1).More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM36640(CHEMBL26514 | L-159,061)
Affinity DataIC50: 1.00E+5nMpH: 7.0 T: 2°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using dehydropeptidase 1 (DPH-1).More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM36639(L-158-817)
Affinity DataIC50: 1.00E+5nMpH: 7.0 T: 2°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using dehydropeptidase 1 (DPH-1).More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM36643(L-161,189)
Affinity DataIC50: 1.20E+5nMpH: 7.0 T: 2°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using dehydropeptidase 1 (DPH-1).More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM36645(CHEMBL291582 | L-707,581)
Affinity DataIC50: 1.90E+5nMpH: 7.0 T: 2°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using dehydropeptidase 1 (DPH-1).More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM36638(L-158-678)
Affinity DataIC50: 2.40E+5nMpH: 7.0 T: 2°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using dehydropeptidase 1 (DPH-1).More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM36637(L-809-558)
Affinity DataIC50: 2.50E+5nMpH: 7.0 T: 2°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using dehydropeptidase 1 (DPH-1).More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM36636(L-809-559)
Affinity DataIC50: 2.50E+5nMpH: 7.0 T: 2°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using dehydropeptidase 1 (DPH-1).More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM36635(L-808,509)
Affinity DataIC50: 5.00E+5nMpH: 7.0 T: 2°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using dehydropeptidase 1 (DPH-1).More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM36634(L-158,507)
Affinity DataIC50: 1.00E+6nMpH: 7.0 T: 2°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using dehydropeptidase 1 (DPH-1).More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetDipeptidase 1(Human)
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM36633(L-809,022)
Affinity DataIC50: 1.00E+6nMpH: 7.0 T: 2°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using dehydropeptidase 1 (DPH-1).More data for this Ligand-Target Pair
In DepthDetails Article
PubMed