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Found 20 with Last Name = 'shim' and Initial = 'jh'
TargetTrans-sialidase(Trypanosoma cruzi)
University of British Columbia

LigandPNGBDBM84698(Quinolinone derivative, 9)
Affinity DataKi:  400nM ΔG°:  -37.7kJ/mole IC50:  600nMpH: 7.6 T: 2°CAssay Description:Inhibition assay using trans-sialidase, a membrane-associated protein.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTrans-sialidase(Trypanosoma cruzi)
University of British Columbia

LigandPNGBDBM50174833(CHEMBL199442 | N-(3-(3-(3,4-dihydroxyphenyl)acrylo...)
Affinity DataKi:  3.70E+3nM ΔG°:  -32.0kJ/mole IC50:  2.50E+3nMpH: 7.6 T: 2°CAssay Description:Inhibition assay using trans-sialidase, a membrane-associated protein.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTrans-sialidase(Trypanosoma cruzi)
University of British Columbia

LigandPNGBDBM50174837(4'-(p-toluenesulfonamide)-3,4-dihydroxy chalcone |...)
Affinity DataKi:  4.60E+3nM ΔG°:  -31.5kJ/mole IC50:  900nMpH: 7.6 T: 2°CAssay Description:Inhibition assay using trans-sialidase, a membrane-associated protein.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional purine biosynthesis protein ATIC(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50089572(2-{4-[(2-Amino-4-oxo-3,4-dihydro-quinazolin-6-ylme...)
Affinity DataKi:  1.70E+4nMAssay Description:In vitro inhibitory activity against Aminoimidazole carboxamide ribonucleotide transformylaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTrifunctional purine biosynthetic protein adenosine-3(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50089585(2,6-Diamino-5-[2-(4,5-difluoro-2-nitro-phenylamino...)
Affinity DataKi:  3.50E+4nMAssay Description:In vitro inhibitory activity against Glycinamide ribonucleotide transformylase (GAR Tfase) after 3 min at 250 uMMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTrifunctional purine biosynthetic protein adenosine-3(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50089594(2-{4-[(2-Amino-4-oxo-3,4-dihydro-quinazolin-6-ylme...)
Affinity DataKi:  4.50E+4nMAssay Description:In vitro inhibitory activity against Glycinamide ribonucleotide transformylase (GAR Tfase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional purine biosynthesis protein ATIC(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50089594(2-{4-[(2-Amino-4-oxo-3,4-dihydro-quinazolin-6-ylme...)
Affinity DataKi:  5.20E+4nMAssay Description:In vitro inhibitory activity against Aminoimidazole carboxamide ribonucleotide transformylaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTrifunctional purine biosynthetic protein adenosine-3(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50089572(2-{4-[(2-Amino-4-oxo-3,4-dihydro-quinazolin-6-ylme...)
Affinity DataKi: >1.00E+5nMAssay Description:In vitro inhibitory activity against Glycinamide ribonucleotide transformylase (GAR Tfase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRNA-directed RNA polymerase(Hepatitis C virus)
Valeant Pharmaceuticals International

Curated by ChEMBL
LigandPNGBDBM50410390(CHEMBL1161754)
Affinity DataKi:  2.01E+5nMAssay Description:Inhibition constant against ATP binding towards Hepatitis C Virus NS5BRdRpMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRNA-directed RNA polymerase(Hepatitis C virus)
Valeant Pharmaceuticals International

Curated by ChEMBL
LigandPNGBDBM50410391(CHEMBL1161753)
Affinity DataKi:  2.29E+5nMAssay Description:Inhibition constant against ATP binding towards Hepatitis C Virus NS5BRdRpMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRNA-directed RNA polymerase(Hepatitis C virus)
Valeant Pharmaceuticals International

Curated by ChEMBL
LigandPNGBDBM50410392(CHEMBL1161773)
Affinity DataKi:  3.27E+5nMAssay Description:Inhibition constant against ATP binding towards Hepatitis C Virus NS5BRdRpMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Valeant Research And Development

Curated by ChEMBL
LigandPNGBDBM50476133(CHEMBL373571 | VRX-480773)
Affinity DataIC50:  4nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetBifunctional purine biosynthesis protein ATIC(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50369444(CHEMBL608337)
Affinity DataIC50:  125nMAssay Description:Inhibitory activity against AICAR formyltransferaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional purine biosynthesis protein ATIC(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50080319(10-Formyl-8-deazafolic acid | CHEMBL114215)
Affinity DataIC50:  6.40E+3nMAssay Description:Inhibitory activity against AICAR formyltransferaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional purine biosynthesis protein ATIC(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM22579(AICAR | Aminoimidazole-4-carboxamide ribonucleotid...)
Affinity DataIC50:  2.50E+4nMAssay Description:Inhibitory activity against AICAR formyltransferaseMore data for this Ligand-Target Pair
TargetTrans-sialidase(Trypanosoma cruzi)
University of British Columbia

LigandPNGBDBM84697(Quinolinone derivative, 8)
Affinity DataIC50:  3.00E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition assay using trans-sialidase, a membrane-associated protein.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTrans-sialidase(Trypanosoma cruzi)
University of British Columbia

LigandPNGBDBM50174834(CHEMBL382280 | N-(3-(3-(4-hydroxyphenyl)acryloyl)p...)
Affinity DataIC50:  3.70E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition assay using trans-sialidase, a membrane-associated protein.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional purine biosynthesis protein ATIC(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50080320((2R)-2-{[4-(N-{[(6R)-2-amino-4-oxo-1,4,4a,5,6,7,8,...)
Affinity DataIC50:  5.00E+4nMAssay Description:Inhibitory activity against AICAR formyltransferaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTrans-sialidase(Trypanosoma cruzi)
University of British Columbia

LigandPNGBDBM50174835(4'-(4-toluenesulfonamido)-4-hydroxychalcone | 4'-(...)
Affinity DataIC50:  7.30E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition assay using trans-sialidase, a membrane-associated protein.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional purine biosynthesis protein ATIC(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50369444(CHEMBL608337)
Affinity DataKd:  20nMAssay Description:Binding affinity towards AICAR formyltransferaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed