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Found 230 with Last Name = 'kim' and Initial = 'ch'
TargetCytidine deaminase(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50367349(CHEMBL604436)
Affinity DataKi:  0.100nMAssay Description:Compound was tested for the inhibitory constant for mouse kidney cytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50391219(CHEMBL2093931)
Affinity DataKi:  100nMAssay Description:Compound was tested for the inhibitory constant for mouse kidney cytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50367346(CHEMBL605877)
Affinity DataKi:  400nMAssay Description:Compound was tested for the inhibitory constant for mouse kidney cytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50421666(CHEMBL2311128 | US9040501, 876404)
Affinity DataKi:  400nMAssay Description:Compound was tested for the inhibitory constant for mouse kidney cytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine deaminase(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50226311(CHEBI:46938 | Zebularine)
Affinity DataKi:  1.00E+3nMAssay Description:Compound was tested for the inhibitory constant for adenosine deaminase (ADA)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50226311(CHEBI:46938 | Zebularine)
Affinity DataKi:  2.00E+3nMAssay Description:Compound was tested for the inhibitory constant for mouse kidney cytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50367344(CHEMBL1232227 | CHEMBL604639)
Affinity DataKi:  4.00E+3nMAssay Description:Compound was tested for the inhibitory constant for mouse kidney cytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50367345(CHEMBL604220)
Affinity DataKi:  4.00E+3nMAssay Description:Compound was tested for the inhibitory constant for mouse kidney cytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50367348(CHEMBL3218780 | CHEMBL604226)
Affinity DataKi:  1.00E+4nMAssay Description:Compound was tested for the inhibitory constant for mouse kidney cytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50335291(9-(beta-D-ribofuranosyl)purine | CHEMBL1399702 | n...)
Affinity DataKi:  1.00E+4nMAssay Description:Compound was tested for the inhibitory constant for mouse kidney cytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50367351(CHEMBL604221)
Affinity DataKi:  2.00E+4nMAssay Description:Compound was tested for the inhibitory constant for mouse kidney cytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50367347(CHEMBL605678)
Affinity DataKi:  1.00E+5nMAssay Description:Compound was tested for the inhibitory constant for mouse kidney cytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK3(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50193995(3-((3R,4R)-4-methyl-3-(methyl(7H-pyrrolo[2,3-d]pyr...)
Affinity DataIC50:  0.240nMAssay Description:Inhibition of JAK3 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK2(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM412676(US10399979, Compound 17c)
Affinity DataIC50:  0.890nMAssay Description:Inhibition of JAK2 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK3(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM412680(US10399979, Compound 17d)
Affinity DataIC50:  1nMAssay Description:Inhibition of JAK3 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK2(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM412674(US10399979, Compound 17a)
Affinity DataIC50:  1.10nMAssay Description:Inhibition of JAK2 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK3(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM412676(US10399979, Compound 17c)
Affinity DataIC50:  1.10nMAssay Description:Inhibition of JAK3 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK2(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50193995(3-((3R,4R)-4-methyl-3-(methyl(7H-pyrrolo[2,3-d]pyr...)
Affinity DataIC50:  1.10nMAssay Description:Inhibition of JAK2 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
TargetTyrosine-protein kinase JAK1(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM412687(US10399979, Compound 18)
Affinity DataIC50:  1.20nMAssay Description:Inhibition of JAK1 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK1(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50193995(3-((3R,4R)-4-methyl-3-(methyl(7H-pyrrolo[2,3-d]pyr...)
Affinity DataIC50:  1.40nMAssay Description:Inhibition of JAK1 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
TargetTyrosine-protein kinase JAK3(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM412675(US10399979, Compound 17b)
Affinity DataIC50:  1.70nMAssay Description:Inhibition of JAK3 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK2(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM412680(US10399979, Compound 17d)
Affinity DataIC50:  1.80nMAssay Description:Inhibition of JAK2 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK1(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM412673(US10399979, Compound 13c)
Affinity DataIC50:  1.90nMAssay Description:Inhibition of JAK1 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails ArticlePubMed
TargetNon-receptor tyrosine-protein kinase TYK2(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM412674(US10399979, Compound 17a)
Affinity DataIC50:  1.90nMAssay Description:Inhibition of TYK2 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Korea University

Curated by ChEMBL
LigandPNGBDBM50334712((R,E)-3-(2-Fluoro-benzenesulfonyl)-thiazolidine-2-...)
Affinity DataIC50:  2nMAssay Description:Inhibition of human 11beta-HSD1 expressed in CHO cells after 3 hrs by HTRF cortisol assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Korea University

Curated by ChEMBL
LigandPNGBDBM50334712((R,E)-3-(2-Fluoro-benzenesulfonyl)-thiazolidine-2-...)
Affinity DataIC50:  2nMAssay Description:Inhibition of human 11beta-HSD1 expressed in CHO cells after 3 hrs by HTRF cortisol assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNon-receptor tyrosine-protein kinase TYK2(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM412676(US10399979, Compound 17c)
Affinity DataIC50:  2.20nMAssay Description:Inhibition of TYK2 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK3(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM412687(US10399979, Compound 18)
Affinity DataIC50:  2.60nMAssay Description:Inhibition of JAK3 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK3(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM412674(US10399979, Compound 17a)
Affinity DataIC50:  2.90nMAssay Description:Inhibition of JAK3 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Korea University

Curated by ChEMBL
LigandPNGBDBM50334708((E)-3-[(2-Fluorophenyl)sulfonyl]-N-[5-(aminocarbon...)
Affinity DataIC50:  3nMAssay Description:Inhibition of human 11beta-HSD1 expressed in CHO cells after 3 hrs by HTRF cortisol assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Korea University

Curated by ChEMBL
LigandPNGBDBM50334708((E)-3-[(2-Fluorophenyl)sulfonyl]-N-[5-(aminocarbon...)
Affinity DataIC50:  3nMAssay Description:Inhibition of human 11beta-HSD1 expressed in CHO cells after 3 hrs by HTRF cortisol assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK2(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM412687(US10399979, Compound 18)
Affinity DataIC50:  3.10nMAssay Description:Inhibition of JAK2 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK1(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM412690(US10399979, Compound 20a)
Affinity DataIC50:  3.40nMAssay Description:Inhibition of JAK1 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK2(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM412675(US10399979, Compound 17b)
Affinity DataIC50:  3.60nMAssay Description:Inhibition of JAK2 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Mus musculus (mouse))
Korea University

Curated by ChEMBL
LigandPNGBDBM50334709(3-(3-Fluoro-benzenesulfonyl)-thiazolidine-2-carbox...)
Affinity DataIC50:  4nMAssay Description:Inhibition of mouse 11beta-HSD1 expressed in CHO cells after 3 hrs by HTRF cortisol assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK1(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM412674(US10399979, Compound 17a)
Affinity DataIC50:  4.20nMAssay Description:Inhibition of JAK1 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails ArticlePubMed
TargetNon-receptor tyrosine-protein kinase TYK2(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM412687(US10399979, Compound 18)
Affinity DataIC50:  4.40nMAssay Description:Inhibition of TYK2 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Korea University

Curated by ChEMBL
LigandPNGBDBM50334704(3-(3,4-Dichloro-benzenesulfonyl)-thiazolidine-2-ca...)
Affinity DataIC50:  5nMAssay Description:Inhibition of human 11beta-HSD1 expressed in CHO cells after 3 hrs by HTRF cortisol assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK1(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50466000(CHEMBL4287893)
Affinity DataIC50:  5.30nMAssay Description:Inhibition of JAK1 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Rattus norvegicus (rat))
National Institutes Of Health

Curated by ChEMBL
LigandPNGBDBM50017082((+)-trans-N-{1-[2-(4-Isothiocyanato-phenyl)-ethyl]...)
Affinity DataIC50:  6nMAssay Description:The ability of comp[ound to inhibit [3H]-DADL binding to the delta receptor of the NG108-15 cells at 10 min and 37 degree CMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Mus musculus (mouse))
Korea University

Curated by ChEMBL
LigandPNGBDBM50334705(3-Benzenesulfonyl-thiazolidine-2-carboxylic acid(5...)
Affinity DataIC50:  6nMAssay Description:Inhibition of mouse 11beta-HSD1 expressed in CHO cells after 3 hrs by HTRF cortisol assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK1(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM412676(US10399979, Compound 17c)
Affinity DataIC50:  6.60nMAssay Description:Inhibition of JAK1 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK3(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM412672(US10399979, Compound 13b)
Affinity DataIC50:  6.70nMAssay Description:Inhibition of JAK3 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Korea University

Curated by ChEMBL
LigandPNGBDBM50334706(3-(Toluene-4-sulfonyl)-thiazolidine-2-carboxylic a...)
Affinity DataIC50:  8nMAssay Description:Inhibition of human 11beta-HSD1 expressed in CHO cells after 3 hrs by HTRF cortisol assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNon-receptor tyrosine-protein kinase TYK2(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM412680(US10399979, Compound 17d)
Affinity DataIC50:  8.40nMAssay Description:Inhibition of TYK2 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK2(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50466000(CHEMBL4287893)
Affinity DataIC50:  8.90nMAssay Description:Inhibition of JAK2 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK3(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM412671(US10399979, Compound 13a)
Affinity DataIC50:  9.90nMAssay Description:Inhibition of JAK3 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK1(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM412672(US10399979, Compound 13b)
Affinity DataIC50:  9.90nMAssay Description:Inhibition of JAK1 (unknown origin) preincubated for 20 mins followed by [33P]-ATP addition measured after 2 hrs by filter-binding methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Korea University

Curated by ChEMBL
LigandPNGBDBM50334694(3-Benzenesulfonyl-thiazolidine-2-carboxylic acid a...)
Affinity DataIC50:  10nMAssay Description:Inhibition of human 11beta-HSD1 expressed in CHO cells after 3 hrs by HTRF cortisol assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Korea University

Curated by ChEMBL
LigandPNGBDBM50334701(3-(3,4-Dichloro-benzenesulfonyl)-thiazolidine-2-ca...)
Affinity DataIC50:  10nMAssay Description:Inhibition of human 11beta-HSD1 expressed in CHO cells after 3 hrs by HTRF cortisol assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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