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Found 17 Enz. Inhib. hit(s) with Target = 'Glycylpeptide N-tetradecanoyltransferase 2'
TargetGlycylpeptide N-tetradecanoyltransferase 2(Homo sapiens (Human))
Imperial College

Curated by ChEMBL
LigandPNGBDBM50384914(CHEMBL2036496 | CHEMBL2079453)
Affinity DataKi:  1.14E+4nMAssay Description:Inhibition of human N-myristoyltransferase 2 using human pp60Src92-16 amino acids) as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycylpeptide N-tetradecanoyltransferase 2(Homo sapiens (Human))
Imperial College

Curated by ChEMBL
LigandPNGBDBM50384911(CHEMBL2036500)
Affinity DataKi:  2.32E+4nMAssay Description:Inhibition of human N-myristoyltransferase 2 using human pp60Src92-16 amino acids) as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycylpeptide N-tetradecanoyltransferase 2(Homo sapiens (Human))
Imperial College

Curated by ChEMBL
LigandPNGBDBM50384923(CHEMBL2036636)
Affinity DataKi:  3.75E+4nMAssay Description:Inhibition of human N-myristoyltransferase 2 using human pp60Src92-16 amino acids) as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycylpeptide N-tetradecanoyltransferase 2(Homo sapiens (Human))
Imperial College

Curated by ChEMBL
LigandPNGBDBM50384916(CHEMBL2036504)
Affinity DataKi:  4.15E+4nMAssay Description:Inhibition of human N-myristoyltransferase 2 using human pp60Src92-16 amino acids) as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycylpeptide N-tetradecanoyltransferase 2(Homo sapiens (Human))
Imperial College

Curated by ChEMBL
LigandPNGBDBM50384920(CHEMBL2036508)
Affinity DataKi:  4.61E+4nMAssay Description:Inhibition of human N-myristoyltransferase 2 using human pp60Src92-16 amino acids) as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycylpeptide N-tetradecanoyltransferase 2(Homo sapiens (Human))
Imperial College

Curated by ChEMBL
LigandPNGBDBM50384917(CHEMBL2036505)
Affinity DataKi:  9.42E+4nMAssay Description:Inhibition of human N-myristoyltransferase 2 using human pp60Src92-16 amino acids) as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycylpeptide N-tetradecanoyltransferase 2(Homo sapiens (Human))
Imperial College

Curated by ChEMBL
LigandPNGBDBM50384922(CHEMBL1339047)
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of human N-myristoyltransferase 2 using human pp60Src92-16 amino acids) as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycylpeptide N-tetradecanoyltransferase 2(Homo sapiens (Human))
Imperial College

Curated by ChEMBL
LigandPNGBDBM33749(3-(6-Bromo-3-butyl-2-methyl-quinolin-4-ylsulfanyl)...)
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of human N-myristoyltransferase 2 using human pp60Src92-16 amino acids) as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycylpeptide N-tetradecanoyltransferase 2(Homo sapiens (Human))
Imperial College

Curated by ChEMBL
LigandPNGBDBM50384921(CHEMBL2036510)
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of human N-myristoyltransferase 2 using human pp60Src92-16 amino acids) as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycylpeptide N-tetradecanoyltransferase 2(Homo sapiens (Human))
Imperial College

Curated by ChEMBL
LigandPNGBDBM50384919(CHEMBL2036507)
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of human N-myristoyltransferase 2 using human pp60Src92-16 amino acids) as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycylpeptide N-tetradecanoyltransferase 2(Homo sapiens (Human))
Imperial College

Curated by ChEMBL
LigandPNGBDBM50384925(CHEMBL2036638)
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of human N-myristoyltransferase 2 using human pp60Src92-16 amino acids) as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycylpeptide N-tetradecanoyltransferase 2(Homo sapiens (Human))
Imperial College

Curated by ChEMBL
LigandPNGBDBM50384915(CHEMBL2036503)
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of human N-myristoyltransferase 2 using human pp60Src92-16 amino acids) as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycylpeptide N-tetradecanoyltransferase 2(Homo sapiens (Human))
Imperial College

Curated by ChEMBL
LigandPNGBDBM50384912(CHEMBL2036502)
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of human N-myristoyltransferase 2 using human pp60Src92-16 amino acids) as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycylpeptide N-tetradecanoyltransferase 2(Homo sapiens (Human))
Imperial College

Curated by ChEMBL
LigandPNGBDBM50384913(CHEMBL2036501)
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of human N-myristoyltransferase 2 using human pp60Src92-16 amino acids) as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycylpeptide N-tetradecanoyltransferase 2(Homo sapiens (Human))
Imperial College

Curated by ChEMBL
LigandPNGBDBM50384918(CHEMBL2036506)
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of human N-myristoyltransferase 2 using human pp60Src92-16 amino acids) as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycylpeptide N-tetradecanoyltransferase 2(Homo sapiens (Human))
Imperial College

Curated by ChEMBL
LigandPNGBDBM50384924(CHEMBL2036637)
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of human N-myristoyltransferase 2 using human pp60Src92-16 amino acids) as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycylpeptide N-tetradecanoyltransferase 2(Homo sapiens (Human))
Imperial College

Curated by ChEMBL
LigandPNGBDBM50364113(CHEMBL1230468)
Affinity DataIC50:  3nMAssay Description:Inhibition of human N-myristoyltransferase 2 assessed as transfer of [3H]-myristic acid to a biotinylated substrate peptide (GCGGSKVKPQPPQAK(biotin)-...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed