Compile Data Set for Download or QSAR
maximum 50k data
Found 39 Enz. Inhib. hit(s) with all data for entry = 50039341
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335107(5-(4-aminopyridin-3-yl)-1,3,4-thiadiazol-2-amine |...)
Affinity DataKi:  2.00E+3nMAssay Description:Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335105(2-(5-Amino-[1,3,4]thiadiazol-2-yl)-4H-chromen-4-on...)
Affinity DataKi:  2.00E+3nMAssay Description:Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335104(3-(5-Amino-[1,3,4]thiadiazol-2-yl)-1-(thiophen-2-y...)
Affinity DataKi:  2.00E+3nMAssay Description:Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335098(6-Nitro-benzothiazol-2-ylamine | 6-nitrobenzo[d]th...)
Affinity DataKi:  3.00E+3nMAssay Description:Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM30705(CHEMBL744 | MLS000069369 | RILUZOLE | SMR000058231...)
Affinity DataKi:  4.00E+3nMAssay Description:Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335102(3-Chloro-N-[5-(2-chloroethyl)-[1,3,4]thiadiazol-2-...)
Affinity DataKi:  7.00E+3nMAssay Description:Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335103(3-(5-Amino-[1,3,4]thiadiazol-2-yl)-1-(4-chlorophen...)
Affinity DataKi:  7.00E+3nMAssay Description:Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335101(2-(1,3-Dioxoisoindolin-2-yl)-N-5-(1,3-dioxoisoindo...)
Affinity DataKi:  9.00E+3nMAssay Description:Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335097(6-(methylsulfonyl)benzo[d]thiazol-2-amine | 6-Meth...)
Affinity DataKi:  1.60E+4nMAssay Description:Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335106(5-(1H-benzo[d][1,2,3]triazol-5-yl)-[1,3,4]thiadiaz...)
Affinity DataKi:  2.40E+4nMAssay Description:Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335099(4-chlorobenzo[d]thiazol-2-amine | CHEMBL1413383 | ...)
Affinity DataKi:  7.90E+4nMAssay Description:Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335100(1,3-benzothiazol-2-amine | 2-Aminobenzothiazole, 6...)
Affinity DataKi:  1.43E+5nMAssay Description:Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335110(CHEMBL1650237 | [1,3,4]Thiadiazol-2-ylamine)
Affinity DataKi:  4.36E+5nMAssay Description:Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335105(2-(5-Amino-[1,3,4]thiadiazol-2-yl)-4H-chromen-4-on...)
Affinity DataIC50:  2.20E+4nMAssay Description:Inhibition of Leishmania major PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335104(3-(5-Amino-[1,3,4]thiadiazol-2-yl)-1-(thiophen-2-y...)
Affinity DataIC50:  2.90E+4nMAssay Description:Inhibition of Leishmania major PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335107(5-(4-aminopyridin-3-yl)-1,3,4-thiadiazol-2-amine |...)
Affinity DataIC50:  3.10E+4nMAssay Description:Inhibition of Leishmania major PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335098(6-Nitro-benzothiazol-2-ylamine | 6-nitrobenzo[d]th...)
Affinity DataIC50:  4.00E+4nMAssay Description:Inhibition of Leishmania major PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM30705(CHEMBL744 | MLS000069369 | RILUZOLE | SMR000058231...)
Affinity DataIC50:  5.00E+4nMAssay Description:Inhibition of Leishmania major PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335103(3-(5-Amino-[1,3,4]thiadiazol-2-yl)-1-(4-chlorophen...)
Affinity DataIC50:  8.90E+4nMAssay Description:Inhibition of Leishmania major PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335102(3-Chloro-N-[5-(2-chloroethyl)-[1,3,4]thiadiazol-2-...)
Affinity DataIC50:  9.30E+4nMAssay Description:Inhibition of Leishmania major PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335101(2-(1,3-Dioxoisoindolin-2-yl)-N-5-(1,3-dioxoisoindo...)
Affinity DataIC50:  1.16E+5nMAssay Description:Inhibition of Leishmania major PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional dihydrofolate reductase-thymidylate synthase(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335104(3-(5-Amino-[1,3,4]thiadiazol-2-yl)-1-(thiophen-2-y...)
Affinity DataIC50:  1.39E+5nMAssay Description:Inhibition of Leishmania major DHFRMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335097(6-(methylsulfonyl)benzo[d]thiazol-2-amine | 6-Meth...)
Affinity DataIC50:  2.12E+5nMAssay Description:Inhibition of Leishmania major PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydrofolate reductase(Homo sapiens (Human))
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335104(3-(5-Amino-[1,3,4]thiadiazol-2-yl)-1-(thiophen-2-y...)
Affinity DataIC50:  3.00E+5nMAssay Description:Inhibition of human DHFRMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335106(5-(1H-benzo[d][1,2,3]triazol-5-yl)-[1,3,4]thiadiaz...)
Affinity DataIC50:  3.09E+5nMAssay Description:Inhibition of Leishmania major PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydrofolate reductase(Homo sapiens (Human))
Rutgers University

Curated by ChEMBL
LigandPNGBDBM30705(CHEMBL744 | MLS000069369 | RILUZOLE | SMR000058231...)
Affinity DataIC50:  3.12E+5nMAssay Description:Inhibition of human DHFRMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM10443(2-methylquinolin-4-amine | 4-Aminoquinaldine 4)
Affinity DataIC50:  3.90E+5nMAssay Description:Inhibition of Leishmania major PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335099(4-chlorobenzo[d]thiazol-2-amine | CHEMBL1413383 | ...)
Affinity DataIC50:  1.00E+6nMAssay Description:Inhibition of Leishmania major PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335109(1-methyl-1H-indazol-5-amine | CHEMBL1650263)
Affinity DataIC50:  1.00E+6nMAssay Description:Inhibition of Leishmania major PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydrofolate reductase(Homo sapiens (Human))
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335097(6-(methylsulfonyl)benzo[d]thiazol-2-amine | 6-Meth...)
Affinity DataIC50:  1.04E+6nMAssay Description:Inhibition of human DHFRMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50182880(CHEMBL147741 | indole-3-carboxaldehyde)
Affinity DataIC50:  1.10E+6nMAssay Description:Inhibition of Leishmania major PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional dihydrofolate reductase-thymidylate synthase(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335105(2-(5-Amino-[1,3,4]thiadiazol-2-yl)-4H-chromen-4-on...)
Affinity DataIC50:  1.30E+6nMAssay Description:Inhibition of Leishmania major DHFRMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional dihydrofolate reductase-thymidylate synthase(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335099(4-chlorobenzo[d]thiazol-2-amine | CHEMBL1413383 | ...)
Affinity DataIC50:  1.39E+6nMAssay Description:Inhibition of Leishmania major DHFRMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional dihydrofolate reductase-thymidylate synthase(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335097(6-(methylsulfonyl)benzo[d]thiazol-2-amine | 6-Meth...)
Affinity DataIC50:  1.79E+6nMAssay Description:Inhibition of Leishmania major DHFRMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335100(1,3-benzothiazol-2-amine | 2-Aminobenzothiazole, 6...)
Affinity DataIC50:  1.80E+6nMAssay Description:Inhibition of Leishmania major PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM10458(4-AP | 4-Aminopyridine 10 | CHEMBL284348 | DALFAMP...)
Affinity DataIC50:  1.90E+6nMAssay Description:Inhibition of Leishmania major PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional dihydrofolate reductase-thymidylate synthase(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50182880(CHEMBL147741 | indole-3-carboxaldehyde)
Affinity DataIC50:  2.00E+6nMAssay Description:Inhibition of Leishmania major DHFRMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335108((4-Fluorophenyl)-(4-hydroxy-phenyl)-methanone | CH...)
Affinity DataIC50:  2.30E+6nMAssay Description:Inhibition of Leishmania major PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPteridine reductase 1(Leishmania major)
Rutgers University

Curated by ChEMBL
LigandPNGBDBM50335110(CHEMBL1650237 | [1,3,4]Thiadiazol-2-ylamine)
Affinity DataIC50:  5.60E+6nMAssay Description:Inhibition of Leishmania major PTR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed