Compile Data Set for Download or QSAR
maximum 50k data
Found 33 of ic50 for UniProtKB: A0A140VJI3
TargetDipeptidase 1(Homo sapiens (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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (Human))
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148531(2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...)
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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (Human))
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148532(2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...)
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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (Human))
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148533(2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...)
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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (Human))
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148531(2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...)
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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (Human))
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148530(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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (Human))
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148528(2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...)
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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (Human))
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148532(2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...)
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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (Human))
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148533(2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...)
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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (Human))
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148530(2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...)
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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (Human))
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

Curated by ChEMBL
LigandPNGBDBM50148528(2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...)
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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (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
In DepthDetails ArticlePubMed
TargetDipeptidase 1(Homo sapiens (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
In DepthDetails ArticlePubMed
TargetDipeptidase 1(Homo sapiens (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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (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
In DepthDetails ArticlePubMed
TargetDipeptidase 1(Homo sapiens (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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (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
In DepthDetails ArticlePubMed
TargetDipeptidase 1(Homo sapiens (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
In DepthDetails ArticlePubMed
TargetDipeptidase 1(Homo sapiens (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
In DepthDetails ArticlePubMed
TargetDipeptidase 1(Homo sapiens (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
In DepthDetails ArticlePubMed
TargetDipeptidase 1(Homo sapiens (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 ArticlePubMed
TargetDipeptidase 1(Homo sapiens (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 ArticlePubMed