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Found 47 with Last Name = 'sousa' and Initial = 'e'
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Ciimar

Curated by ChEMBL
LigandPNGBDBM50031612(CHEMBL3354688)
Affinity DataKi:  660nMAssay Description:Binding affinity to human ERG assessed as inhibition constantMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Ciimar

Curated by ChEMBL
LigandPNGBDBM50601401(CHEMBL5201184)
Affinity DataIC50:  1.10nMAssay Description:Inhibition of BACE1 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetC-C chemokine receptor type 1(Homo sapiens (Human))
Ciimar

Curated by ChEMBL
LigandPNGBDBM50451624(CHEMBL331897)
Affinity DataIC50:  1.20nMAssay Description:Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Ciimar

Curated by ChEMBL
LigandPNGBDBM50031612(CHEMBL3354688)
Affinity DataIC50:  2nMAssay Description:Inhibition of BACE1 (unknown origin)More data for this Ligand-Target Pair
TargetC-C chemokine receptor type 1(Homo sapiens (Human))
Ciimar

Curated by ChEMBL
LigandPNGBDBM50098641(1-Cyclooct-1-enylmethyl-1-ethyl-4-[(9H-xanthene-9-...)
Affinity DataIC50:  2nMAssay Description:Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCoagulation factor X(Homo sapiens (Human))
Universidade Do Porto (Cequimed-Up)

Curated by ChEMBL
LigandPNGBDBM7840(RIVAROXABAN | US8822458, 44 | US8822458, 97)
Affinity DataIC50:  4.59nMAssay Description:Inhibition of human factor 10a assessed as CBS 31.39 substrate hydrolysis by spectrophotometric analysisMore data for this Ligand-Target Pair
TargetC-C chemokine receptor type 1(Homo sapiens (Human))
Ciimar

Curated by ChEMBL
LigandPNGBDBM50098634(1-Cyclooctylmethyl-1-methyl-4-[(9H-xanthene-9-carb...)
Affinity DataIC50:  14nMAssay Description:Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetC-C chemokine receptor type 1(Homo sapiens (Human))
Ciimar

Curated by ChEMBL
LigandPNGBDBM50098650(9H-Xanthene-9-carboxylic acid (1-cyclooctylmethyl-...)
Affinity DataIC50:  140nMAssay Description:Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetC-C chemokine receptor type 1(Homo sapiens (Human))
Ciimar

Curated by ChEMBL
LigandPNGBDBM50098629(9H-Xanthene-9-carboxylic acid (1-cyclohexylmethyl-...)
Affinity DataIC50:  200nMAssay Description:Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetC-C chemokine receptor type 1(Homo sapiens (Human))
Ciimar

Curated by ChEMBL
LigandPNGBDBM50098625(9H-Xanthene-9-carboxylic acid (1-hexyl-piperidin-4...)
Affinity DataIC50:  510nMAssay Description:Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetC-C chemokine receptor type 1(Homo sapiens (Human))
Ciimar

Curated by ChEMBL
LigandPNGBDBM50098647(9H-Xanthene-9-carboxylic acid (1-cyclodecylmethyl-...)
Affinity DataIC50:  800nMAssay Description:Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50549267(CHEMBL4760852)
Affinity DataIC50:  1.90E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50549268(CHEMBL4762659)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50549265(CHEMBL4763799)
Affinity DataIC50:  2.24E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50549274(CHEMBL3093489)
Affinity DataIC50:  3.01E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50549271(CHEMBL4754324)
Affinity DataIC50:  3.16E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50549269(CHEMBL4792623)
Affinity DataIC50:  3.28E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50549264(CHEMBL4167922)
Affinity DataIC50:  3.37E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50155444(3-Hydroxy-4-methoxy-xanthen-9-one | CHEMBL185895)
Affinity DataIC50:  3.81E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50549276(CHEMBL4175535)
Affinity DataIC50:  4.02E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50549277(CHEMBL4060966)
Affinity DataIC50:  4.42E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50268290(1,7-Dihydroxyxanthone | CHEBI:4946 | CHEMBL389166)
Affinity DataIC50:  4.52E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50155428(3,4-Dimethoxy-xanthen-9-one | CHEMBL186020)
Affinity DataIC50:  5.12E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50269645(3,4-dihydroxyxanthone | CHEMBL446323 | US9114126, ...)
Affinity DataIC50:  5.12E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50155442(3-Methoxy-xanthen-9-one | CHEMBL186368)
Affinity DataIC50:  5.14E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50155412(1-Methoxy-xanthen-9-one | CHEMBL364619)
Affinity DataIC50:  5.14E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50155441(4-Hydroxy-3-methoxy-xanthen-9-one | CHEMBL186863)
Affinity DataIC50:  5.20E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50155416(4-Methoxy-xanthen-9-one | CHEMBL187801)
Affinity DataIC50:  5.33E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50549266(CHEMBL4762742)
Affinity DataIC50:  5.57E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50155409(2-Hydroxy-xanthen-9-one | CHEMBL185960)
Affinity DataIC50:  5.60E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50549278(CHEMBL4168741)
Affinity DataIC50:  5.70E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50549279(CHEMBL2297451)
Affinity DataIC50:  7.80E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50549275(CHEMBL1434162)
Affinity DataIC50:  8.29E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50155413(4-Hydroxy-xanthen-9-one | CHEMBL359978)
Affinity DataIC50:  8.46E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50155417(2-Methoxy-xanthen-9-one | CHEMBL186609)
Affinity DataIC50:  8.47E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50155415(1-Hydroxy-xanthen-9-one | 1-Hydroxyxanthone | 1-hy...)
Affinity DataIC50:  8.83E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50155411(9-oxoxanthene | 9-xanthenone | 9-xanthone | 9H-xan...)
Affinity DataIC50:  8.84E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50549270(CHEMBL4793245)
Affinity DataIC50:  8.93E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50155408(3-Hydroxy-xanthen-9-one | CHEMBL365640)
Affinity DataIC50:  9.26E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetC-C chemokine receptor type 1(Homo sapiens (Human))
Ciimar

Curated by ChEMBL
LigandPNGBDBM50098646(9H-Xanthene-9-carboxylic acid (1-benzyl-piperidin-...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetC-C chemokine receptor type 1(Homo sapiens (Human))
Ciimar

Curated by ChEMBL
LigandPNGBDBM50098623(9H-Xanthene-9-carboxylic acid (1-naphthalen-2-ylme...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50031467(5-HYDROXY-2-(HYDROXYMETHYL)-4H-PYRAN-4-ONE | 5-Hyd...)
Affinity DataIC50:  1.28E+4nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50549272(CHEMBL4175123)
Affinity DataIC50:  2.91E+4nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Universidade Dos A£Ores

Curated by ChEMBL
LigandPNGBDBM50549273(CHEMBL4166817)
Affinity DataIC50:  8.94E+4nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAntithrombin-III/Coagulation factor X(Homo sapiens (Human))
Universidade Do Porto (Cequimed-Up)

Curated by ChEMBL
LigandPNGBDBM50393527(CHEMBL2158198)
Affinity DataIC50:  1.90E+5nMAssay Description:Inhibition of human factor 10a/antithrombin 3 assessed as CBS 31.39 substrate hydrolysis by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Universidade Do Porto (Cequimed-Up)

Curated by ChEMBL
LigandPNGBDBM50393527(CHEMBL2158198)
Affinity DataIC50:  7.40E+5nMAssay Description:Inhibition of human factor 10a assessed as CBS 31.39 substrate hydrolysis by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Universidade Do Porto (Cequimed-Up)

Curated by ChEMBL
LigandPNGBDBM50393526(CHEMBL2158201)
Affinity DataIC50:  9.70E+5nMAssay Description:Inhibition of human factor 10a assessed as CBS 31.39 substrate hydrolysis by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed