Report error Found 171 with Last Name = 'whitman' and Initial = 'db'
Affinity DataKd: 0.0600nMAssay Description:Dissociation constant of radiolabeled compound binding to alpha-v-beta-3More data for this Ligand-Target Pair
Affinity DataIC50: 0.0700nMAssay Description:Displacement of [125I]nonpeptide ligand (compound 7) from purified human recombinant alphaV-beta3More data for this Ligand-Target Pair
Affinity DataIC50: 0.0800nMAssay Description:Displacement of [125I]nonpeptide ligand (compound 7) from purified human recombinant alphaV-beta3More data for this Ligand-Target Pair
Affinity DataIC50: 0.100nMAssay Description:Displacement of [125I]echistatin from human recombinant alpha-v beta-3 receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 0.100nMAssay Description:Inhibition of alpha v beta 3 receptor bindingMore data for this Ligand-Target Pair
Affinity DataIC50: 0.300nMAssay Description:Displacement of [125I]echistatin from human recombinant alpha-v beta-3 receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 0.300nMAssay Description:Inhibition of alpha v beta 3 receptor bindingMore data for this Ligand-Target Pair
Affinity DataIC50: 0.350nMAssay Description:Displacement of a non-peptide radioligand from human recombinant alphaV-beta3 integrinMore data for this Ligand-Target Pair
Affinity DataIC50: 0.400nMAssay Description:Inhibition of alpha v beta 3 receptor bindingMore data for this Ligand-Target Pair
Affinity DataIC50: 0.400nMAssay Description:Displacement of [125I]echistatin from human recombinant alpha-v beta-3 receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 0.440nMAssay Description:Displacement of [125I]nonpeptide ligand (compound 7) from purified human recombinant alphaV-beta3More data for this Ligand-Target Pair
Affinity DataIC50: 0.670nMAssay Description:Inhibition of binding to human alpha V beta3More data for this Ligand-Target Pair
Affinity DataIC50: 0.700nMAssay Description:Displacement of [125I]echistatin from human recombinant alpha-v beta-3 receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 0.800nMAssay Description:Inhibition of binding to alpha v beta 3 receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 0.800nMAssay Description:Inhibition of alpha v beta 3 receptor bindingMore data for this Ligand-Target Pair
Affinity DataIC50: 0.930nMAssay Description:Displacement of [125I]nonpeptide ligand (compound 7) from purified human recombinant alphaV-beta3More data for this Ligand-Target Pair
Affinity DataIC50: 0.940nMAssay Description:Displacement of a non-peptide radioligand from human recombinant alphaV-beta3 integrinMore data for this Ligand-Target Pair
Affinity DataIC50: 1.20nMAssay Description:Displacement of a non-peptide radioligand from human recombinant alphaV-beta3 integrinMore data for this Ligand-Target Pair
Affinity DataIC50: 1.30nMAssay Description:Displacement of a non-peptide radioligand from human recombinant alphaV-beta3 integrinMore data for this Ligand-Target Pair
Affinity DataIC50: 1.5nMAssay Description:Inhibition of binding to human alpha V beta3More data for this Ligand-Target Pair
Affinity DataIC50: 1.60nMAssay Description:Inhibition of binding to human alpha V beta3More data for this Ligand-Target Pair
Affinity DataIC50: 1.80nMAssay Description:Displacement of [125I]echistatin from human recombinant alpha-v beta-3 receptorMore data for this Ligand-Target Pair
TargetA disintegrin and metalloproteinase with thrombospondin motifs 5(Human)
Merck Research Laboratories
Merck Research Laboratories
Affinity DataIC50: 1.90nMpH: 7.0 T: 2°CAssay Description:The kinesin motor domain is incubated with microtubules, 1 mM ATP (1: 1 MgCl2 : Na-ATP), and compound at 23°C in buffer. After reaction was term...More data for this Ligand-Target Pair
Affinity DataIC50: 2.30nMAssay Description:Inhibition of alpha v beta 3 receptor bindingMore data for this Ligand-Target Pair
Affinity DataIC50: 2.90nMAssay Description:Displacement of a non-peptide radioligand from human recombinant alphaV-beta3 integrinMore data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:Inhibition of binding to human alpha V beta3More data for this Ligand-Target Pair
Affinity DataIC50: 3.30nMAssay Description:Inhibition of binding to human alpha V beta3More data for this Ligand-Target Pair
Affinity DataIC50: 4.70nMAssay Description:Inhibition of binding to alpha v beta 3 receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 5.80nMAssay Description:Inhibition of binding to human alpha V beta3More data for this Ligand-Target Pair
Affinity DataIC50: 5.90nMAssay Description:Inhibition of binding to human alpha V beta3More data for this Ligand-Target Pair
Affinity DataIC50: 6.10nMAssay Description:Inhibition of binding to alpha v beta 3 receptorMore data for this Ligand-Target Pair
TargetA disintegrin and metalloproteinase with thrombospondin motifs 5(Human)
Merck Research Laboratories
Merck Research Laboratories
Affinity DataIC50: 8nMpH: 7.0 T: 2°CAssay Description:The kinesin motor domain is incubated with microtubules, 1 mM ATP (1: 1 MgCl2 : Na-ATP), and compound at 23°C in buffer. After reaction was term...More data for this Ligand-Target Pair
Affinity DataIC50: 8.80nMAssay Description:Displacement of a non-peptide radioligand from human recombinant alphaV-beta3 integrinMore data for this Ligand-Target Pair
Affinity DataIC50: 10.7nMAssay Description:Displacement of [125I]nonpeptide ligand (compound 7) from purified human recombinant alphaV-beta3More data for this Ligand-Target Pair
Affinity DataIC50: 11.2nMAssay Description:Inhibition of binding to alpha v beta 3 receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 12nMAssay Description:Displacement of a non-peptide radioligand from human recombinant alphaV-beta3 integrinMore data for this Ligand-Target Pair
Affinity DataIC50: 13nMAssay Description:Inhibition of binding to human alpha V beta3More data for this Ligand-Target Pair
Affinity DataIC50: 18nMAssay Description:Antagonist activity at human OX2R expressed in CHO cells assessed as inhibition of orexin-A-induced intracellular calcium mobilization after 5 mins b...More data for this Ligand-Target Pair
Affinity DataIC50: 18.1nMAssay Description:Inhibition of binding to alpha v beta 3 receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 19.3nMpH: 7.4 T: 2°CAssay Description:The hERG IC50 values were determined by radioligand competition experiments using membrane preparations from human embryonic kidney cells that stably...More data for this Ligand-Target Pair
Affinity DataIC50: 21.3nMAssay Description:Inhibition of binding to alpha v beta 3 receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 23nMAssay Description:Inhibition of KSP in KBV1 cells overexpressing PgpMore data for this Ligand-Target Pair
Affinity DataIC50: 23nMAssay Description:Inhibition of binding to human alpha V beta3More data for this Ligand-Target Pair
Affinity DataIC50: 24nMAssay Description:Inhibition of KSP in KB31 cellsMore data for this Ligand-Target Pair







































