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Found 21 Enz. Inhib. hit(s) with all data for entry = 50040325
TargetDihydrofolate reductase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50392653(CHEMBL2153707)
Affinity DataIC50:  18nMAssay Description:Inhibition of human recombinant DHFR using dihydrofolate as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydrofolate reductase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50392656(CHEMBL2153711)
Affinity DataIC50:  32nMAssay Description:Inhibition of human recombinant DHFR using dihydrofolate as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydrofolate reductase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50392658(CHEMBL2151066)
Affinity DataIC50:  33nMAssay Description:Inhibition of human recombinant DHFR using dihydrofolate as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydrofolate reductase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50392654(CHEMBL2153709)
Affinity DataIC50:  33nMAssay Description:Inhibition of human recombinant DHFR using dihydrofolate as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydrofolate reductase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50392657(CHEMBL2153705)
Affinity DataIC50:  420nMAssay Description:Inhibition of human recombinant DHFR using dihydrofolate as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydrofolate reductase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50392650(CHEMBL2153704)
Affinity DataIC50:  800nMAssay Description:Inhibition of human recombinant DHFR using dihydrofolate as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydrofolate reductase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50392655(CHEMBL2153710)
Affinity DataIC50:  1.07E+3nMAssay Description:Inhibition of human recombinant DHFR using dihydrofolate as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMethionine synthase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50392652(CHEMBL2153714)
Affinity DataIC50:  1.43E+3nMAssay Description:Inhibition of methionine synthase in human HL60 cells using L-homocysteine as substrate incubated for 3 hrs prior to substrate addition measured afte...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMethionine synthase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50392649(CHEMBL2153712)
Affinity DataIC50:  1.73E+3nMAssay Description:Inhibition of methionine synthase in human HL60 cells using L-homocysteine as substrate incubated for 3 hrs prior to substrate addition measured afte...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMethionine synthase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50392656(CHEMBL2153711)
Affinity DataIC50:  8.11E+3nMAssay Description:Inhibition of methionine synthase in human HL60 cells using L-homocysteine as substrate incubated for 3 hrs prior to substrate addition measured afte...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMethionine synthase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50392661(CHEMBL2153703)
Affinity DataIC50:  1.59E+4nMAssay Description:Inhibition of methionine synthase in human HL60 cells using L-homocysteine as substrate incubated for 3 hrs prior to substrate addition measured afte...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMethionine synthase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50392651(CHEMBL2153713)
Affinity DataIC50:  2.10E+4nMAssay Description:Inhibition of methionine synthase in human HL60 cells using L-homocysteine as substrate incubated for 3 hrs prior to substrate addition measured afte...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMethionine synthase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50392660(CHEMBL2153706)
Affinity DataIC50:  2.78E+4nMAssay Description:Inhibition of methionine synthase in human HL60 cells using L-homocysteine as substrate incubated for 3 hrs prior to substrate addition measured afte...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMethionine synthase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50392655(CHEMBL2153710)
Affinity DataIC50:  5.50E+4nMAssay Description:Inhibition of methionine synthase in human HL60 cells using L-homocysteine as substrate incubated for 3 hrs prior to substrate addition measured afte...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMethionine synthase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50392650(CHEMBL2153704)
Affinity DataIC50:  6.64E+4nMAssay Description:Inhibition of methionine synthase in human HL60 cells using L-homocysteine as substrate incubated for 3 hrs prior to substrate addition measured afte...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMethionine synthase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50392659(CHEMBL2153708)
Affinity DataIC50:  8.79E+4nMAssay Description:Inhibition of methionine synthase in human HL60 cells using L-homocysteine as substrate incubated for 3 hrs prior to substrate addition measured afte...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMethionine synthase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50392657(CHEMBL2153705)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of methionine synthase in human HL60 cells using L-homocysteine as substrate incubated for 3 hrs prior to substrate addition measured afte...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydrofolate reductase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50392649(CHEMBL2153712)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human recombinant DHFR using dihydrofolate as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMethionine synthase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50392654(CHEMBL2153709)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of methionine synthase in human HL60 cells using L-homocysteine as substrate incubated for 3 hrs prior to substrate addition measured afte...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMethionine synthase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50392653(CHEMBL2153707)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of methionine synthase in human HL60 cells using L-homocysteine as substrate incubated for 3 hrs prior to substrate addition measured afte...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMethionine synthase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50392658(CHEMBL2151066)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of methionine synthase in human HL60 cells using L-homocysteine as substrate incubated for 3 hrs prior to substrate addition measured afte...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed