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Found 361 with Last Name = 'grädler' and Initial = 'u'
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Nycomed

Curated by ChEMBL
LigandPNGBDBM50386178(CHEMBL1800346 | ONO-1714)
Affinity DataKi:  1.86nMAssay Description:Inhibition of human iNOS assessed as inhibition of [3H]L-arginine to [3H]L-citrulline conversion by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, endothelial(Homo sapiens (Human))
Nycomed

Curated by ChEMBL
LigandPNGBDBM50386178(CHEMBL1800346 | ONO-1714)
Affinity DataKi:  18.6nMAssay Description:Inhibition of human eNOS assessed as inhibition of [3H]L-arginine to [3H]L-citrulline conversion by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetQueuine tRNA-ribosyltransferase(Zymomonas mobilis)
Philipps-UniversitäT Marburg

Curated by ChEMBL
LigandPNGBDBM50125769(2,6-Diamino-8-phenylsulfanylmethyl-3H-quinazolin-4...)
Affinity DataKi:  100nMAssay Description:Inhibitory activity against eubacterial tRNA guanine transglycosylase (TGT) from Zymomonas mobilisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetQueuine tRNA-ribosyltransferase(Zymomonas mobilis)
Philipps-UniversitäT Marburg

Curated by ChEMBL
LigandPNGBDBM50125773(2-Amino-6-methyl-3H-pteridin-4-one | CHEMBL14913)
Affinity DataKi:  250nMAssay Description:Inhibitory activity against eubacterial tRNA guanine transglycosylase (TGT) from Zymomonas mobilisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetQueuine tRNA-ribosyltransferase(Zymomonas mobilis)
Philipps-UniversitäT Marburg

Curated by ChEMBL
LigandPNGBDBM50125771(6-Amino-2,3-dihydro-benzo[g]phthalazine-1,4-dione ...)
Affinity DataKi:  300nMAssay Description:Inhibitory activity against eubacterial tRNA guanine transglycosylase (TGT) from Zymomonas mobilisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetQueuine tRNA-ribosyltransferase(Zymomonas mobilis)
Philipps-UniversitäT Marburg

Curated by ChEMBL
LigandPNGBDBM50125772(2-amino-4-hydroxypteridine | 2-aminopteridin-4-ol ...)
Affinity DataKi:  600nMAssay Description:Inhibitory activity against eubacterial tRNA guanine transglycosylase (TGT) from Zymomonas mobilisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetQueuine tRNA-ribosyltransferase(Zymomonas mobilis)
Philipps-UniversitäT Marburg

Curated by ChEMBL
LigandPNGBDBM50125760(2-Amino-8-(4-chloro-benzylsulfanyl)-1,9-dihydro-pu...)
Affinity DataKi:  2.70E+3nMAssay Description:Inhibitory activity against eubacterial tRNA guanine transglycosylase (TGT) from Zymomonas mobilisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetQueuine tRNA-ribosyltransferase(Zymomonas mobilis)
Philipps-UniversitäT Marburg

Curated by ChEMBL
LigandPNGBDBM50125766(2-Amino-7-phenyl-3H-pteridin-4-one | CHEMBL277561)
Affinity DataKi:  3.80E+3nMAssay Description:Inhibitory activity against eubacterial tRNA guanine transglycosylase (TGT) from Zymomonas mobilisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetQueuine tRNA-ribosyltransferase(Zymomonas mobilis)
Philipps-UniversitäT Marburg

Curated by ChEMBL
LigandPNGBDBM50125761(3-Methyl-6,7-dihydro-4H-1-thia-4,6,7-triaza-cyclop...)
Affinity DataKi:  4.70E+3nMAssay Description:Inhibitory activity against eubacterial tRNA guanine transglycosylase (TGT) from Zymomonas mobilisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetQueuine tRNA-ribosyltransferase(Zymomonas mobilis)
Philipps-UniversitäT Marburg

Curated by ChEMBL
LigandPNGBDBM50125768(6,7-Dihydro-4H-1-thia-4,6,7-triaza-cyclopenta[b]na...)
Affinity DataKi:  5.00E+3nMAssay Description:Inhibitory activity against eubacterial tRNA guanine transglycosylase (TGT) from Zymomonas mobilisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetQueuine tRNA-ribosyltransferase(Zymomonas mobilis)
Philipps-UniversitäT Marburg

Curated by ChEMBL
LigandPNGBDBM50125765(3-Amino-6-hydroxy-2-(2-hydroxy-ethyl)-2,5-dihydro-...)
Affinity DataKi:  8.10E+3nMAssay Description:Inhibitory activity against eubacterial tRNA guanine transglycosylase (TGT) from Zymomonas mobilisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetQueuine tRNA-ribosyltransferase(Zymomonas mobilis)
Philipps-UniversitäT Marburg

Curated by ChEMBL
LigandPNGBDBM50125767(4-AMINOPHTHALHYDRAZIDE | 6-Amino-2,3-dihydro-phtha...)
Affinity DataKi:  8.30E+3nMAssay Description:Inhibitory activity against eubacterial tRNA guanine transglycosylase (TGT) from Zymomonas mobilisMore data for this Ligand-Target Pair
TargetQueuine tRNA-ribosyltransferase(Zymomonas mobilis)
Philipps-UniversitäT Marburg

Curated by ChEMBL
LigandPNGBDBM50125759(5-Amino-2,3-dihydro-phthalazine-1,4-dione | CHEMBL...)
Affinity DataKi:  3.60E+4nMAssay Description:Inhibitory activity against eubacterial tRNA guanine transglycosylase (TGT) from Zymomonas mobilisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetQueuine tRNA-ribosyltransferase(Zymomonas mobilis)
Philipps-UniversitäT Marburg

Curated by ChEMBL
LigandPNGBDBM50125775(2-Amino-8-piperidin-1-yl-1,9-dihydro-purin-6-one |...)
Affinity DataKi:  3.70E+4nMAssay Description:Inhibitory activity against eubacterial tRNA guanine transglycosylase (TGT) from Zymomonas mobilisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetQueuine tRNA-ribosyltransferase(Zymomonas mobilis)
Philipps-UniversitäT Marburg

Curated by ChEMBL
LigandPNGBDBM50125774(5-Fluoro-1H-indole-2-carboxylic acid hydrazide | C...)
Affinity DataKi:  7.20E+4nMAssay Description:Inhibitory activity against eubacterial tRNA guanine transglycosylase (TGT) from Zymomonas mobilisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetQueuine tRNA-ribosyltransferase(Zymomonas mobilis)
Philipps-UniversitäT Marburg

Curated by ChEMBL
LigandPNGBDBM50125763(2-BUTYL-5,6-DIHYDRO-1H-IMIDAZO[4,5-D]PYRIDAZINE-4,...)
Affinity DataKi:  8.30E+4nMAssay Description:Inhibitory activity against eubacterial tRNA guanine transglycosylase (TGT) from Zymomonas mobilisMore data for this Ligand-Target Pair
TargetQueuine tRNA-ribosyltransferase(Zymomonas mobilis)
Philipps-UniversitäT Marburg

Curated by ChEMBL
LigandPNGBDBM50125770(6-Methyl-2H-pyrazolo[3,4-b]quinolin-3-ylamine | CH...)
Affinity DataKi:  1.56E+5nMAssay Description:Inhibitory activity against eubacterial tRNA guanine transglycosylase (TGT) from Zymomonas mobilisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetQueuine tRNA-ribosyltransferase(Zymomonas mobilis)
Philipps-UniversitäT Marburg

Curated by ChEMBL
LigandPNGBDBM50125762(5,6-Dihydro-1H-imidazo[4,5-d]pyridazine-4,7-dione ...)
Affinity DataKi:  2.00E+5nMAssay Description:Inhibitory activity against eubacterial tRNA guanine transglycosylase (TGT) from Zymomonas mobilisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetQueuine tRNA-ribosyltransferase(Zymomonas mobilis)
Philipps-UniversitäT Marburg

Curated by ChEMBL
LigandPNGBDBM50125764(3-Amino-6-phenyl-2,7-dihydro-pyrazolo[3,4-d]pyrimi...)
Affinity DataKi:  2.49E+5nMAssay Description:Inhibitory activity against eubacterial tRNA guanine transglycosylase (TGT) from Zymomonas mobilisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50318884(CHEMBL1084546 | CHEMBL2430359 | N-methyl-N-(3-((2-...)
Affinity DataIC50:  1.5nMAssay Description:Competitive binding affinity to FAK kinase domain (410 to 689) (unknown origin) assessed as phosphorylation of p(Glu/Tyr) in presence of ATPMore data for this Ligand-Target Pair
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50425681(CHEMBL2315564)
Affinity DataIC50:  37nMAssay Description:Inhibition of FAK (unknown origin) using biotinylated His-TEV-hsFAK(31-686)(K454R) substrate after 2 hrs by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50425672(CHEMBL2315584)
Affinity DataIC50:  37nMAssay Description:Inhibition of FAK (unknown origin) using biotinylated His-TEV-hsFAK(31-686)(K454R) substrate after 2 hrs by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Nycomed

Curated by ChEMBL
LigandPNGBDBM50124535(1-(6-CYANO-3-PYRIDYLCARBONYL)-5',8'-DIFLUOROSPIRO[...)
Affinity DataIC50:  37.1nMAssay Description:Inhibition of human iNOS assessed as inhibition of [3H]L-arginine to [3H]L-citrulline conversion by scintillation countingMore data for this Ligand-Target Pair
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Nycomed

Curated by ChEMBL
LigandPNGBDBM50418856(CHEMBL1800534)
Affinity DataIC50:  38.9nMAssay Description:Inhibition of human iNOS assessed as inhibition of [3H]L-arginine to [3H]L-citrulline conversion by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, endothelial(Homo sapiens (Human))
Nycomed

Curated by ChEMBL
LigandPNGBDBM50091805(2-amino-4,6-dimethylpyridine | 4,6-Dimethyl-pyridi...)
Affinity DataIC50:  44.7nMAssay Description:Inhibition of human eNOS assessed as inhibition of [3H]L-arginine to [3H]L-citrulline conversion by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50425686(CHEMBL2315566)
Affinity DataIC50:  45nMAssay Description:Inhibition of FAK (unknown origin) using biotinylated His-TEV-hsFAK(31-686)(K454R) substrate after 2 hrs by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50425687(CHEMBL2315565)
Affinity DataIC50:  45nMAssay Description:Inhibition of FAK (unknown origin) using biotinylated His-TEV-hsFAK(31-686)(K454R) substrate after 2 hrs by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50425679(CHEMBL2315562)
Affinity DataIC50:  51nMAssay Description:Inhibition of FAK (unknown origin) using biotinylated His-TEV-hsFAK(31-686)(K454R) substrate after 2 hrs by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Nycomed

Curated by ChEMBL
LigandPNGBDBM50418855(CHEMBL1800533)
Affinity DataIC50:  55.0nMAssay Description:Inhibition of human iNOS assessed as inhibition of [3H]L-arginine to [3H]L-citrulline conversion by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50425688(CHEMBL2315563)
Affinity DataIC50:  57nMAssay Description:Inhibition of FAK (unknown origin) using biotinylated His-TEV-hsFAK(31-686)(K454R) substrate after 2 hrs by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-beta(Homo sapiens (Human))
Merck Serono

Curated by ChEMBL
LigandPNGBDBM50386043(CHEMBL2042883)
Affinity DataIC50:  60nMAssay Description:Displacement of [3H]17AAG from human recombinant Hsp90 after 30 mins by beta scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Nycomed

Curated by ChEMBL
LigandPNGBDBM50418844(CHEMBL1800347)
Affinity DataIC50:  70.8nMAssay Description:Inhibition of human iNOS assessed as inhibition of [3H]L-arginine to [3H]L-citrulline conversion by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Nycomed

Curated by ChEMBL
LigandPNGBDBM50418849(CHEMBL1738840)
Affinity DataIC50:  81.3nMAssay Description:Inhibition of human iNOS assessed as inhibition of [3H]L-arginine to [3H]L-citrulline conversion by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50425687(CHEMBL2315565)
Affinity DataIC50:  83nMAssay Description:Inhibition of FAK in human HT-29 cells assessed as phosphorylation at tyrosine 397 after 45 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50425686(CHEMBL2315566)
Affinity DataIC50:  107nMAssay Description:Inhibition of FAK in human HT-29 cells assessed as phosphorylation at tyrosine 397 after 45 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Nycomed

Curated by ChEMBL
LigandPNGBDBM50091805(2-amino-4,6-dimethylpyridine | 4,6-Dimethyl-pyridi...)
Affinity DataIC50:  110nMAssay Description:Inhibition of human iNOS assessed as inhibition of [3H]L-arginine to [3H]L-citrulline conversion by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Nycomed

Curated by ChEMBL
LigandPNGBDBM50418845(CHEMBL1800348)
Affinity DataIC50:  115nMAssay Description:Inhibition of human iNOS assessed as inhibition of [3H]L-arginine to [3H]L-citrulline conversion by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50425685(CHEMBL2315572)
Affinity DataIC50:  130nMAssay Description:Inhibition of FAK (unknown origin) using biotinylated His-TEV-hsFAK(31-686)(K454R) substrate after 2 hrs by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Nycomed

Curated by ChEMBL
LigandPNGBDBM50418851(CHEMBL1800528)
Affinity DataIC50:  145nMAssay Description:Inhibition of human iNOS assessed as inhibition of [3H]L-arginine to [3H]L-citrulline conversion by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-beta(Homo sapiens (Human))
Merck Serono

Curated by ChEMBL
LigandPNGBDBM50386053(CHEMBL2042769)
Affinity DataIC50:  150nMAssay Description:Displacement of [3H]17AAG from human recombinant Hsp90 after 30 mins by beta scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Nycomed

Curated by ChEMBL
LigandPNGBDBM50418847(CHEMBL1800523)
Affinity DataIC50:  155nMAssay Description:Inhibition of human iNOS assessed as inhibition of [3H]L-arginine to [3H]L-citrulline conversion by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50425684(CHEMBL2315571)
Affinity DataIC50:  170nMAssay Description:Inhibition of FAK (unknown origin) using biotinylated His-TEV-hsFAK(31-686)(K454R) substrate after 2 hrs by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-beta(Homo sapiens (Human))
Merck Serono

Curated by ChEMBL
LigandPNGBDBM50386047(CHEMBL2042764)
Affinity DataIC50:  170nMAssay Description:Displacement of [3H]17AAG from human recombinant Hsp90 after 30 mins by beta scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50425673(CHEMBL2315580)
Affinity DataIC50:  177nMAssay Description:Inhibition of FAK (unknown origin) using biotinylated His-TEV-hsFAK(31-686)(K454R) substrate after 2 hrs by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Nycomed

Curated by ChEMBL
LigandPNGBDBM50418860(CHEMBL1800526)
Affinity DataIC50:  186nMAssay Description:Inhibition of human iNOS assessed as inhibition of [3H]L-arginine to [3H]L-citrulline conversion by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50425675(CHEMBL2315579)
Affinity DataIC50:  195nMAssay Description:Inhibition of FAK (unknown origin) using biotinylated His-TEV-hsFAK(31-686)(K454R) substrate after 2 hrs by scintillation counting analysisMore data for this Ligand-Target Pair
TargetHeat shock protein HSP 90-beta(Homo sapiens (Human))
Merck Serono

Curated by ChEMBL
LigandPNGBDBM50386051(CHEMBL2042767)
Affinity DataIC50:  200nMAssay Description:Displacement of [3H]17AAG from human recombinant Hsp90 after 30 mins by beta scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50425667(CHEMBL2315583)
Affinity DataIC50:  220nMAssay Description:Inhibition of FAK (unknown origin) using biotinylated His-TEV-hsFAK(31-686)(K454R) substrate after 2 hrs by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-beta(Homo sapiens (Human))
Merck Serono

Curated by ChEMBL
LigandPNGBDBM50386005(CHEMBL2042895)
Affinity DataIC50:  230nMAssay Description:Displacement of [3H]17AAG from human recombinant Hsp90 after 30 mins by beta scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-beta(Homo sapiens (Human))
Merck Serono

Curated by ChEMBL
LigandPNGBDBM50386031(CHEMBL2042870)
Affinity DataIC50:  250nMAssay Description:Displacement of [3H]17AAG from human recombinant Hsp90 after 30 mins by beta scintillation countingMore data for this Ligand-Target Pair
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