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Found 602 with Last Name = 'maj' and Initial = 'r'
LigandPNGBDBM92649(EPZ004777)
Affinity DataKi:  0.300nM Kd:  0.100nMAssay Description:Assay of DOT1L enzymatic activity were performed under balanced conditions using a radiometric assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM92648(EPZ004450)
Affinity DataKi:  4nMAssay Description:Assay of DOT1L enzymatic activity were performed under balanced conditions using a radiometric assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM92647(EPZ003696)
Affinity DataKi:  13nMAssay Description:Assay of DOT1L enzymatic activity were performed under balanced conditions using a radiometric assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Sib Swiss Institute Of Bioinformatics

Curated by ChEMBL
LigandPNGBDBM34233(2-Phenyl-benzo[d]isoselenazol-3-one | 2-Phenyl-ben...)
Affinity DataKi:  94nMAssay Description:Inhibition of human recombinant IDO1 using L-tryptophan as substrate preincubated for 5 mins followed by substrate addition measured after 10 mins by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Sib Swiss Institute Of Bioinformatics

Curated by ChEMBL
LigandPNGBDBM81348(β-Lapachone (A3) | Beta lapachone | R115 (Rea...)
Affinity DataKi:  100nMAssay Description:Noncompetitive inhibition of human recombinant IDO1 expressed in Escherichia coli by Michaelis-Menton nonlinear regression plot analysis in presence ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM92642(SAH)
Affinity DataKi:  320nM Kd:  71nMAssay Description:Assay of DOT1L enzymatic activity were performed under balanced conditions using a radiometric assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM92646(EPZ003647)
Affinity DataKi:  845nM Kd:  167nMAssay Description:Assay of DOT1L enzymatic activity were performed under balanced conditions using a radiometric assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Sib Swiss Institute Of Bioinformatics

Curated by ChEMBL
LigandPNGBDBM50183456(CHEMBL425403 | N-methyl-N'-9-phenanthrylimidodicar...)
Affinity DataKi:  1.50E+3nMAssay Description:Inhibition of human recombinant IDO1 expressed in yeast IS20-2B using tryptophan as substrate by methylene blue/ascorbate assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Sib Swiss Institute Of Bioinformatics

Curated by ChEMBL
LigandPNGBDBM50279937(CHEMBL1985550)
Affinity DataKi:  4.30E+3nMAssay Description:Inhibition of human recombinant IDO1 using L-tryptophan as substrate after 15 mins by Dixon plot analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Sib Swiss Institute Of Bioinformatics

Curated by ChEMBL
LigandPNGBDBM36371(5-(1H-indol-3-ylmethyl)-3-methyl-2-thioxo-4-Imidaz...)
Affinity DataKi:  1.20E+4nMAssay Description:Competitive inhibition of 6His-tagged human recombinant IDO expressed in Escherichia coli BL21DE3pLysMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM92644(EPZ002446)
Affinity DataKi:  1.20E+4nMAssay Description:Assay of DOT1L enzymatic activity were performed under balanced conditions using a radiometric assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM92645(EPZ003144)
Affinity DataKi:  2.00E+4nMAssay Description:Assay of DOT1L enzymatic activity were performed under balanced conditions using a radiometric assay.More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
LigandPNGBDBM92643(EPZ000004)
Affinity DataKi:  3.80E+4nMAssay Description:Assay of DOT1L enzymatic activity were performed under balanced conditions using a radiometric assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Sib Swiss Institute Of Bioinformatics

Curated by ChEMBL
LigandPNGBDBM50024210(1H-indole-3-ethanamine | 2-(1H-indol-3-yl)ethanami...)
Affinity DataKi:  1.60E+5nMAssay Description:Noncompetitive inhibition of human recombinant IDO1 expressed in Escherichia coli BL21 by Lineweaver-Burk double-reciprocal plot analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Sib Swiss Institute Of Bioinformatics

Curated by ChEMBL
LigandPNGBDBM168435(US9675571, 129)
Affinity DataIC50:  0.5nMAssay Description:Inhibition of human IDO1 in HEK293 cells after 20 hrs by plate reader assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Mus musculus)
Ludwig Center For Cancer Research Of The University Of Lausanne

Curated by ChEMBL
LigandPNGBDBM50391363(CHEMBL2148074)
Affinity DataIC50:  2nMAssay Description:Inhibition of mouse IDO1 in P815 clone 6 cells by HPLC analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
The M.S. University Of Baroda

Curated by ChEMBL
LigandPNGBDBM50478032(CHEMBL275658 | GW4511 | GW564511 | GW69564)
Affinity DataIC50: <2nMAssay Description:Inhibition of wild-type HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The M.S University Of Baroda

Curated by ChEMBL
LigandPNGBDBM50049642(3-Chloro-4,4',5'-trifluoro-4''-methanesulfonyl-[1,...)
Affinity DataIC50:  2nMAssay Description:Inhibition of recombinant human COX-2 expressed in Baculovirus infected sf9 cells using arachidonic acid as substrate preincubated for 10 mins follow...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The M.S University Of Baroda

Curated by ChEMBL
LigandPNGBDBM50288291(3-(4-Methanesulfonyl-phenyl)-4,4-dimethyl-2-phenyl...)
Affinity DataIC50:  2.80nMAssay Description:Inhibition of COX-2 in human whole bloodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Sib Swiss Institute Of Bioinformatics

Curated by ChEMBL
LigandPNGBDBM340834(US9765018, Example 287)
Affinity DataIC50:  3nMAssay Description:Inhibition of human IDO1 in HEK293 cells after 20 hrs by plate reader assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Sib Swiss Institute Of Bioinformatics

Curated by ChEMBL
LigandPNGBDBM317549(3-(3-(3-(2,4- difluorophenyl)ureido)-4- (diisobuty...)
Affinity DataIC50:  3nMAssay Description:Inhibition of human IDO1 in HEK293 cells after 20 hrs by plate reader assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetPeptidase 1(Dermatophagoides pteronyssinus (European house dus...)
Domainex

Curated by ChEMBL
LigandPNGBDBM50031688(CHEMBL3360299)
Affinity DataIC50:  3nMAssay Description:Inhibition of house dust mite Derp-1 after 20 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein arginine N-methyltransferase 5(Homo sapiens (Human))
Epizyme

Curated by ChEMBL
LigandPNGBDBM178085(US10307413, Compound 188 | US10391089, Compound 18...)
Affinity DataIC50:  3nMAssay Description:Inhibition of PRMT5 in human Z138 cells assessed as reduction in symmetrical dimethylation of arginine containing substrate using SmD3 as substrate i...More data for this Ligand-Target Pair
TargetProstaglandin G/H synthase 1(Mus musculus)
The M.S University Of Baroda

Curated by ChEMBL
LigandPNGBDBM50474760(CG-100649 | CG100649 | Polmacoxib)
Affinity DataIC50:  3nMAssay Description:Inhibition of COX-1 in LPS-induced mouse peritoneal macrophagesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The M.S University Of Baroda

Curated by ChEMBL
LigandPNGBDBM50153982(2-(4-Ethoxy-phenyl)-3-(4-methanesulfonyl-phenyl)-p...)
Affinity DataIC50:  3nMAssay Description:Inhibition of human COX-2 expressed in human COS cells using arachidonic acid as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The M.S University Of Baroda

Curated by ChEMBL
LigandPNGBDBM50289328(5-(4-Methanesulfonyl-phenyl)-6-phenyl-2-trifluorom...)
Affinity DataIC50:  3nMAssay Description:Inhibition of recombinant human COX-2 expressed in CHO-K1 cells using arachidonic acid as substrate preincubated for 15 mins followed by substrate ad...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidase 1(Dermatophagoides pteronyssinus (European house dus...)
Domainex

Curated by ChEMBL
LigandPNGBDBM50031689(CHEMBL3360298)
Affinity DataIC50:  3nMAssay Description:Inhibition of house dust mite Derp-1 after 20 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidase 1(Dermatophagoides pteronyssinus (European house dus...)
Domainex

Curated by ChEMBL
LigandPNGBDBM50031684(CHEMBL3360302)
Affinity DataIC50:  4nMAssay Description:Inhibition of house dust mite Derp-1 after 20 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidase 1(Dermatophagoides pteronyssinus (European house dus...)
Domainex

Curated by ChEMBL
LigandPNGBDBM50031685(CHEMBL3360301)
Affinity DataIC50:  4nMAssay Description:Inhibition of house dust mite Derp-1 after 20 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMethylosome protein 50/Protein arginine N-methyltransferase 5(Homo sapiens (Human))
Epizyme

Curated by ChEMBL
LigandPNGBDBM178085(US10307413, Compound 188 | US10391089, Compound 18...)
Affinity DataIC50:  4nMAssay Description:Inhibition of human full length FLAG-tagged PRMT5/human His6-tagged MEP50 expressed in baculovirus-infected Sf9 cells assessed as reduction in tritiu...More data for this Ligand-Target Pair
TargetPeptidase 1(Dermatophagoides pteronyssinus (European house dus...)
Domainex

Curated by ChEMBL
LigandPNGBDBM50031695(CHEMBL3360292)
Affinity DataIC50:  4nMAssay Description:Inhibition of house dust mite Derp-1 after 20 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidase 1(Dermatophagoides pteronyssinus (European house dus...)
Domainex

Curated by ChEMBL
LigandPNGBDBM50031687(CHEMBL3360300)
Affinity DataIC50:  4nMAssay Description:Inhibition of house dust mite Derp-1 after 20 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Sib Swiss Institute Of Bioinformatics

Curated by ChEMBL
LigandPNGBDBM50500137(CHEMBL3747340)
Affinity DataIC50:  5nMAssay Description:Inhibition of human IDO1 in HEK293 cells after 20 hrs by plate reader assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The M.S University Of Baroda

Curated by ChEMBL
LigandPNGBDBM50131593(4-[4-Chloro-5-(3-fluoro-4-methoxy-phenyl)-imidazol...)
Affinity DataIC50:  5nMAssay Description:Inhibition of COX-2 in human 143982 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The M.S University Of Baroda

Curated by ChEMBL
LigandPNGBDBM13063(4-(5-methyl-3-phenyl-1,2-oxazol-4-yl)benzene-1-sul...)
Affinity DataIC50:  5nMAssay Description:Inhibition of recombinant human COX-2 expressed in Baculovirus infected sf9 cells using arachidonic acid as substrate preincubated for 10 mins follow...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidase 1(Dermatophagoides pteronyssinus (European house dus...)
Domainex

Curated by ChEMBL
LigandPNGBDBM50031690(CHEMBL3360297)
Affinity DataIC50:  5nMAssay Description:Inhibition of house dust mite Derp-1 after 20 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidase 1(Dermatophagoides pteronyssinus (European house dus...)
Domainex

Curated by ChEMBL
LigandPNGBDBM50031713(CHEMBL3360282)
Affinity DataIC50:  6nMAssay Description:Inhibition of house dust mite Derp-1 after 20 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidase 1(Dermatophagoides pteronyssinus (European house dus...)
Domainex

Curated by ChEMBL
LigandPNGBDBM50031693(CHEMBL3360294)
Affinity DataIC50:  6nMAssay Description:Inhibition of house dust mite Derp-1 after 20 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidase 1(Dermatophagoides pteronyssinus (European house dus...)
Domainex

Curated by ChEMBL
LigandPNGBDBM50031635(CHEMBL3359786)
Affinity DataIC50:  6nMAssay Description:Inhibition of house dust mite Derp-1 after 20 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidase 1(Dermatophagoides pteronyssinus (European house dus...)
Domainex

Curated by ChEMBL
LigandPNGBDBM50031632(CHEMBL3359790)
Affinity DataIC50:  6nMAssay Description:Inhibition of house dust mite Derp-1 after 20 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidase 1(Dermatophagoides pteronyssinus (European house dus...)
Domainex

Curated by ChEMBL
LigandPNGBDBM103023(US8541363, PVA-039)
Affinity DataIC50:  6.30nMAssay Description:The fluorogenic substrate used for measuring Der p 1 proteolytic activity was 2-aminobenzoylvalylalanylnorleucylseryl-(3-nitro)tyrosinyl aspartamide....More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetPeptidase 1(Dermatophagoides pteronyssinus (European house dus...)
Domainex

Curated by ChEMBL
LigandPNGBDBM50031668(CHEMBL3359782)
Affinity DataIC50:  7nMAssay Description:Inhibition of house dust mite Derp-1 after 20 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Sib Swiss Institute Of Bioinformatics

Curated by ChEMBL
LigandPNGBDBM50126143(Epacadostat | INCB-024360)
Affinity DataIC50:  7.10nMAssay Description:Inhibition of IFN-gamma-stimulated IDO1 activity in human HeLa cells using L-tryptophan as substrate after 48 hrs by microplate reader analysisMore data for this Ligand-Target Pair
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The M.S University Of Baroda

Curated by ChEMBL
LigandPNGBDBM50049041(5-(4-Fluoro-phenyl)-6-(4-methanesulfonyl-phenyl)-s...)
Affinity DataIC50:  7.5nMAssay Description:Inhibition of recombinant human COX-2 expressed in Baculovirus infected sf9 cells using arachidonic acid as substrate preincubated for 10 mins follow...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidase 1(Dermatophagoides pteronyssinus (European house dus...)
Domainex

Curated by ChEMBL
LigandPNGBDBM103022(US8541363, PVA-037)
Affinity DataIC50:  7.85nMAssay Description:The fluorogenic substrate used for measuring Der p 1 proteolytic activity was 2-aminobenzoylvalylalanylnorleucylseryl-(3-nitro)tyrosinyl aspartamide....More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetPeptidase 1(Dermatophagoides pteronyssinus (European house dus...)
Domainex

Curated by ChEMBL
LigandPNGBDBM50031719(CHEMBL3359772)
Affinity DataIC50:  8nMAssay Description:Inhibition of house dust mite Derp-1 after 20 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidase 1(Dermatophagoides pteronyssinus (European house dus...)
Domainex

Curated by ChEMBL
LigandPNGBDBM50031711(CHEMBL3360284)
Affinity DataIC50:  8nMAssay Description:Inhibition of house dust mite Derp-1 after 20 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Telormedix

US Patent
LigandPNGBDBM190405(US9180183, Quinidine)
Affinity DataIC50:  9nMAssay Description:The interaction of SC12 with cytochrome P450 enzymes was tested using Fluorescent High Throughput P450 assays (Gentest); The IC50s of the compounds w...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetCytochrome P450 2D6(Homo sapiens (Human))
Telormedix

US Patent
LigandPNGBDBM190405(US9180183, Quinidine)
Affinity DataIC50:  9nMT: 2°CAssay Description:The interaction of SC12 with cytochrome P450 enzymes was tested using Fluorescent High Throughput P450 assays (Gentest); The IC50s of the compounds w...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetProtein arginine N-methyltransferase 5(Homo sapiens (Human))
Epizyme

Curated by ChEMBL
LigandPNGBDBM177922(US10307413, Compound 337 | US10391089, Compound 16...)
Affinity DataIC50:  9nMAssay Description:Inhibition of PRMT5 in human Z138 cells assessed as reduction in symmetrical dimethylation of arginine containing substrate using SmD3 as substrate i...More data for this Ligand-Target Pair
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