Compile Data Set for Download or QSAR
Report error Found 63 Enz. Inhib. hit(s) with all data for entry = 50040727
TargetHistone deacetylase 1(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399006(CHEMBL2177587)
Affinity DataIC50: 60nMAssay Description:Inhibition of HDAC1 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistone deacetylase 1(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50334366(N-(2-aminophenyl)-3-(4-(1-(2-morpholinoethylamino)...)
Affinity DataIC50: 60nMAssay Description:Inhibition of HDAC1 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistone deacetylase 1(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399004(CHEMBL2177582)
Affinity DataIC50: 100nMAssay Description:Inhibition of HDAC1 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistone deacetylase 1(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399005(CHEMBL2177588)
Affinity DataIC50: 140nMAssay Description:Inhibition of HDAC1 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399005(CHEMBL2177588)
Affinity DataIC50: 200nMAssay Description:Inhibition of HDAC3 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistone deacetylase 2(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399004(CHEMBL2177582)
Affinity DataIC50: 220nMAssay Description:Inhibition of HDAC2 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399006(CHEMBL2177587)
Affinity DataIC50: 230nMAssay Description:Inhibition of HDAC3 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399004(CHEMBL2177582)
Affinity DataIC50: 230nMAssay Description:Inhibition of HDAC3 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistone deacetylase 2(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399006(CHEMBL2177587)
Affinity DataIC50: 250nMAssay Description:Inhibition of HDAC2 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistone deacetylase 2(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399005(CHEMBL2177588)
Affinity DataIC50: 270nMAssay Description:Inhibition of HDAC2 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetCytochrome P450 2D6(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399008(CHEMBL2178223)
Affinity DataIC50: 700nMAssay Description:Inhibition of CYP2D6 in human liver microsomes in presence of NADPH by LC-MS/MS methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistone deacetylase 5(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399005(CHEMBL2177588)
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of HDAC5 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetPolyamine deacetylase HDAC10(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399005(CHEMBL2177588)
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of HDAC10 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetCytochrome P450 3A4(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399007(CHEMBL2178221)
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of CYP3A4 in human liver microsomes in presence of NADPH by LC-MS/MS methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetCytochrome P450 2D6(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399007(CHEMBL2178221)
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of CYP2D6 in human liver microsomes in presence of NADPH by LC-MS/MS methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetCytochrome P450 3A4(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399008(CHEMBL2178223)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of CYP3A4 in human liver microsomes in presence of NADPH by LC-MS/MS methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetCytochrome P450 2C9(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399007(CHEMBL2178221)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of CYP2C9 in human liver microsomes in presence of NADPH by LC-MS/MS methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetPolyamine deacetylase HDAC10(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399006(CHEMBL2177587)
Affinity DataIC50: 3.40E+3nMAssay Description:Inhibition of HDAC10 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistone deacetylase 5(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399006(CHEMBL2177587)
Affinity DataIC50: 3.50E+3nMAssay Description:Inhibition of HDAC5 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetCytochrome P450 3A4(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399004(CHEMBL2177582)
Affinity DataIC50: 4.00E+3nMAssay Description:Inhibition of CYP3A4 in human liver microsomes in presence of NADPH by LC-MS/MS methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetCytochrome P450 2C9(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399008(CHEMBL2178223)
Affinity DataIC50: 4.00E+3nMAssay Description:Inhibition of CYP2C9 in human liver microsomes in presence of NADPH by LC-MS/MS methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399005(CHEMBL2177588)
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of human ERG expressed in CHO cells by patch clamp methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetPolyamine deacetylase HDAC10(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399004(CHEMBL2177582)
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of HDAC10 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetCytochrome P450 2D6(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399006(CHEMBL2177587)
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of CYP2D6 in human liver microsomes in presence of NADPH by LC-MS/MS methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistone deacetylase 5(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399004(CHEMBL2177582)
Affinity DataIC50: 5.30E+3nMAssay Description:Inhibition of HDAC5 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetCytochrome P450 1A2(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399008(CHEMBL2178223)
Affinity DataIC50: 7.00E+3nMAssay Description:Inhibition of CYP1A2 in human liver microsomes in presence of NADPH by LC-MS/MS methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetCytochrome P450 2C19(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399008(CHEMBL2178223)
Affinity DataIC50: 7.00E+3nMAssay Description:Inhibition of CYP2C19 in human liver microsomes in presence of NADPH by LC-MS/MS methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399004(CHEMBL2177582)
Affinity DataIC50: 7.00E+3nMAssay Description:Inhibition of human ERG expressed in CHO cells by patch clamp methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetCytochrome P450 2D6(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399004(CHEMBL2177582)
Affinity DataIC50: 9.00E+3nMAssay Description:Inhibition of CYP2D6 in human liver microsomes in presence of NADPH by LC-MS/MS methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetCytochrome P450 2C19(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399007(CHEMBL2178221)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP2C19 in human liver microsomes in presence of NADPH by LC-MS/MS methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399006(CHEMBL2177587)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human ERG expressed in CHO cells by patch clamp methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetCytochrome P450 2C9(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399004(CHEMBL2177582)
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibition of CYP2C9 in human liver microsomes in presence of NADPH by LC-MS/MS methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistone deacetylase 9(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399005(CHEMBL2177588)
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibition of HDAC9 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistone deacetylase 4(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399006(CHEMBL2177587)
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibition of HDAC4 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetCytochrome P450 3A4(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399006(CHEMBL2177587)
Affinity DataIC50: 1.40E+4nMAssay Description:Inhibition of CYP3A4 in human liver microsomes in presence of NADPH by LC-MS/MS methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistone deacetylase 11(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399006(CHEMBL2177587)
Affinity DataIC50: 1.40E+4nMAssay Description:Inhibition of HDAC11 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399007(CHEMBL2178221)
Affinity DataIC50: 1.50E+4nMAssay Description:Inhibition of human ERG expressed in CHO cells by patch clamp methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistone deacetylase 9(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399006(CHEMBL2177587)
Affinity DataIC50: 1.60E+4nMAssay Description:Inhibition of HDAC9 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistone deacetylase 11(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399005(CHEMBL2177588)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of HDAC11 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetCytochrome P450 3A4(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399005(CHEMBL2177588)
Affinity DataIC50: 2.10E+4nMAssay Description:Inhibition of CYP3A4 in human liver microsomes in presence of NADPH by LC-MS/MS methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetCytochrome P450 2C19(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399004(CHEMBL2177582)
Affinity DataIC50: 2.10E+4nMAssay Description:Inhibition of CYP2C19 in human liver microsomes in presence of NADPH by LC-MS/MS methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetCytochrome P450 2C9(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399005(CHEMBL2177588)
Affinity DataIC50: 2.30E+4nMAssay Description:Inhibition of CYP2C9 in human liver microsomes in presence of NADPH by LC-MS/MS methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetCytochrome P450 1A2(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399007(CHEMBL2178221)
Affinity DataIC50: 2.60E+4nMAssay Description:Inhibition of CYP1A2 in human liver microsomes in presence of NADPH by LC-MS/MS methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetCytochrome P450 1A2(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399004(CHEMBL2177582)
Affinity DataIC50: 2.80E+4nMAssay Description:Inhibition of CYP1A2 in human liver microsomes in presence of NADPH by LC-MS/MS methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetCytochrome P450 2C9(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399006(CHEMBL2177587)
Affinity DataIC50: 2.90E+4nMAssay Description:Inhibition of CYP2C9 in human liver microsomes in presence of NADPH by LC-MS/MS methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistone deacetylase 8(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399004(CHEMBL2177582)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of HDAC8 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistone deacetylase 6(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399006(CHEMBL2177587)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of HDAC6 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistone deacetylase 6(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399004(CHEMBL2177582)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of HDAC6 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistone deacetylase 6(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399005(CHEMBL2177588)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of HDAC6 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistone deacetylase 7(Human)
Roche R & D Center China

Curated by ChEMBL
LigandPNGBDBM50399006(CHEMBL2177587)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of HDAC7 using p53 (379 to 382 residues) based fluorogenic peptide substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
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