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Found 79 with Last Name = 'albert' and Initial = 'mr'
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241226(CHEMBL4079863)
Affinity DataKi:  6.40E+3nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241220(CHEMBL4062721)
Affinity DataKi:  6.70E+3nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241237(CHEMBL4084407)
Affinity DataKi:  8.80E+3nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241228(CHEMBL4093689)
Affinity DataKi:  8.90E+3nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241225(CHEMBL4067612)
Affinity DataKi:  9.10E+3nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241219(CHEMBL4061658)
Affinity DataKi:  1.04E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241224(CHEMBL4092161)
Affinity DataKi:  1.10E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241234(CHEMBL4104504)
Affinity DataKi:  1.12E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241218(CHEMBL4103395)
Affinity DataKi:  1.29E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241239(CHEMBL4072990)
Affinity DataKi:  1.34E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241223(CHEMBL4071367)
Affinity DataKi:  1.47E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50400625(CHEMBL2203469)
Affinity DataKi:  1.74E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241230(CHEMBL4064406)
Affinity DataKi:  2.00E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241232(CHEMBL4097427)
Affinity DataKi:  2.34E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241216(CHEMBL4079148)
Affinity DataKi:  2.35E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by double reciprocal plot methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241241(CHEMBL4102452)
Affinity DataKi:  2.71E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by double reciprocal plot methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50400644(CHEMBL2203460)
Affinity DataKi:  2.89E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241215(CHEMBL4084496)
Affinity DataKi:  3.05E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by double reciprocal plot methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241231(CHEMBL4102329)
Affinity DataKi:  3.21E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241217(CHEMBL4099998)
Affinity DataKi:  3.39E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241214(CHEMBL4094701)
Affinity DataKi:  3.51E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by double reciprocal plot methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241238(CHEMBL4088837)
Affinity DataKi:  3.60E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241229(CHEMBL4085939)
Affinity DataKi:  3.66E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241233(CHEMBL4069260)
Affinity DataKi:  3.87E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241236(CHEMBL4074199)
Affinity DataKi:  4.00E+4nMAssay Description:Binding affinity for human placental microsome cytochrome P450 19A1 with 1 uM [1-beta-3H]-androstenedioneMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241227(CHEMBL4098628)
Affinity DataKi:  4.01E+4nMAssay Description:Binding affinity for human placental microsome cytochrome P450 19A1 with 1 uM [1-beta-3H]-androstenedioneMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241246(CHEMBL4089771)
Affinity DataKi:  4.77E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by double reciprocal plot methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241235(CHEMBL4073135)
Affinity DataKi:  4.81E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50241240(CHEMBL4078058)
Affinity DataKi:  5.21E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-glutamine gamma-glutamyltransferase 2(Homo sapiens (Human))
University Of Ottawa

Curated by ChEMBL
LigandPNGBDBM50400618(CHEMBL2203477)
Affinity DataKi:  6.03E+4nMAssay Description:Irreversible inhibition of human TG2 using AL5 as substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAurora kinase B(Homo sapiens (Human))
Osi Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50437161(CHEMBL2401832)
Affinity DataIC50:  11nMAssay Description:Inhibition of aurora-B (unknown origin) autophosphorylationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMacrophage-stimulating protein receptor(Homo sapiens (Human))
Osi Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50437161(CHEMBL2401832)
Affinity DataIC50:  25nMAssay Description:Inhibition of RON (unknown origin) autophosphorylationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Osi Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50437161(CHEMBL2401832)
Affinity DataIC50:  26nMAssay Description:Inhibition of cMET (unknown origin) using biotinylated poly(Glu,Tyr) as substrate after 60 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Osi Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50437186(CHEMBL2401825)
Affinity DataIC50:  30nMAssay Description:Inhibition of cMET (unknown origin) using biotinylated poly(Glu,Tyr) as substrate after 60 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
Osi Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50437161(CHEMBL2401832)
Affinity DataIC50:  40nMAssay Description:Inhibition of ALK (unknown origin) autophosphorylationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Osi Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50437161(CHEMBL2401832)
Affinity DataIC50:  42nMAssay Description:Inhibition of cMET in human MKN45 cells assessed as phosphorylated MET levels after 4 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Osi Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50437185(CHEMBL2401810)
Affinity DataIC50:  42nMAssay Description:Inhibition of cMET (unknown origin) using biotinylated poly(Glu,Tyr) as substrate after 60 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Osi Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50437171(CHEMBL2401813)
Affinity DataIC50:  47nMAssay Description:Inhibition of cMET (unknown origin) using biotinylated poly(Glu,Tyr) as substrate after 60 minsMore data for this Ligand-Target Pair
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Osi Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50437168(CHEMBL2401818)
Affinity DataIC50:  70nMAssay Description:Inhibition of cMET (unknown origin) using biotinylated poly(Glu,Tyr) as substrate after 60 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Osi Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50437157(CHEMBL2401814)
Affinity DataIC50:  86nMAssay Description:Inhibition of cMET (unknown origin) using biotinylated poly(Glu,Tyr) as substrate after 60 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Osi Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50437184(CHEMBL2401811)
Affinity DataIC50:  89nMAssay Description:Inhibition of cMET (unknown origin) using biotinylated poly(Glu,Tyr) as substrate after 60 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Osi Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50437158(CHEMBL2401740)
Affinity DataIC50:  92nMAssay Description:Inhibition of cMET (unknown origin) using biotinylated poly(Glu,Tyr) as substrate after 60 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Osi Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50437159(CHEMBL2401817)
Affinity DataIC50:  110nMAssay Description:Inhibition of cMET (unknown origin) using biotinylated poly(Glu,Tyr) as substrate after 60 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Osi Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50437183(CHEMBL2401808)
Affinity DataIC50:  110nMAssay Description:Inhibition of cMET (unknown origin) using biotinylated poly(Glu,Tyr) as substrate after 60 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Osi Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50437181(CHEMBL2401816)
Affinity DataIC50:  130nMAssay Description:Inhibition of cMET (unknown origin) using biotinylated poly(Glu,Tyr) as substrate after 60 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Osi Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50437182(CHEMBL2401812)
Affinity DataIC50:  130nMAssay Description:Inhibition of cMET (unknown origin) using biotinylated poly(Glu,Tyr) as substrate after 60 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMacrophage-stimulating protein receptor(Homo sapiens (Human))
Osi Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50437157(CHEMBL2401814)
Affinity DataIC50:  130nMAssay Description:Inhibition of short-form RON (unknown origin) expressed in human HeLa cells assessed as phosphorylated RON levels after 4 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Osi Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50437180(CHEMBL2401820)
Affinity DataIC50:  190nMAssay Description:Inhibition of cMET (unknown origin) using biotinylated poly(Glu,Tyr) as substrate after 60 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMacrophage-stimulating protein receptor(Homo sapiens (Human))
Osi Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50437161(CHEMBL2401832)
Affinity DataIC50:  200nMAssay Description:Inhibition of short-form RON (unknown origin) expressed in human HeLa cells assessed as phosphorylated RON levels after 4 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Osi Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50437179(CHEMBL2401826)
Affinity DataIC50:  200nMAssay Description:Inhibition of cMET (unknown origin) using biotinylated poly(Glu,Tyr) as substrate after 60 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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