Report error Found 521 with Last Name = 'yao' and Initial = 'q'
Affinity DataKi: 0.0700nMAssay Description:Displacement of [3H]U69593 from human kappa opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 0.120nMAssay Description:Displacement of [3H]DAMGO from human mu opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 0.140nMAssay Description:Displacement of [3H]U69593 from human kappa opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 0.170nMAssay Description:Displacement of [3H]naltrindole from human delta opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 0.190nMAssay Description:Displacement of [3H]naltrindole from human delta opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 0.230nMAssay Description:Displacement of [3H]naltrindole from human delta opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 0.350nMAssay Description:Displacement of [3H]naltrindole from human delta opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 0.370nMAssay Description:Displacement of [3H]DAMGO from human mu opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 0.490nMAssay Description:Displacement of [3H]DAMGO from human mu opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 0.640nMAssay Description:Displacement of [3H]U69593 from human kappa opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 1nMAssay Description:Displacement of [3H]U69593 from human kappa opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 1.10nMAssay Description:Displacement of [3H]naltrindole from human delta opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 1.10nMAssay Description:Displacement of [3H]DAMGO from human mu opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 1.40nMAssay Description:Displacement of [3H]U69593 from human kappa opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 1.5nMAssay Description:Displacement of [3H]naltrindole from human delta opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 2.20nMAssay Description:Displacement of [3H]U69593 from human kappa opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 3.90nMAssay Description:Displacement of [3H]DAMGO from human mu opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 4.20nMAssay Description:Displacement of [3H]naltrindole from human delta opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 5.90nMAssay Description:Displacement of [3H]DAMGO from human mu opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 8.70nMAssay Description:Displacement of [3H]naltrindole from human delta opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: <10nMAssay Description:Antagonist activity at dopamine D5 receptor (unknown origin)More data for this Ligand-Target Pair
Affinity DataKi: <10nMAssay Description:Antagonist activity at dopamine D1 receptor (unknown origin)More data for this Ligand-Target Pair
Affinity DataKi: 14nMAssay Description:Displacement of [3H]U69593 from human kappa opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 22nMAssay Description:Displacement of [3H]DAMGO from human mu opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 35nMAssay Description:Displacement of [3H]naltrindole from human delta opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
TargetSphingosine kinase 1(Human)
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Affinity DataKi: 40nMAssay Description:Antagonistic activity against (-)-noradrenaline-induced contraction of rat prostatic vas deferens (Alpha-1A adrenergic receptor )More data for this Ligand-Target Pair
Affinity DataKi: 73nMAssay Description:Agonist activity at dopamine D1 receptor (unknown origin)More data for this Ligand-Target Pair
Affinity DataKi: 89nMAssay Description:Displacement of [3H]U69593 from human kappa opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
TargetSphingosine kinase 2(Human)
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Affinity DataKi: 300nMAssay Description:Inhibition of the cAMP-stimulated beta-galactosidase transcription in SK-N-MC cells expressing the human Histamine H3 receptorMore data for this Ligand-Target Pair
TargetSphingosine kinase 1(Human)
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Affinity DataKi: 300nMAssay Description:Antagonistic activity against (-)-noradrenaline-induced contraction of rat thoracic aorta (Alpha-1D adrenergic receptor)More data for this Ligand-Target Pair
Affinity DataKi: 330nMAssay Description:Displacement of [3H]DAMGO from human mu opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 340nMAssay Description:Displacement of [3H]DAMGO from human mu opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
Affinity DataKi: 390nMAssay Description:Displacement of [3H]U69593 from human kappa opioid receptor expressed in CHO membraneMore data for this Ligand-Target Pair
TargetSphingosine kinase 2(Mouse)
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Affinity DataKi: 400nMAssay Description:Functional Histamine H1 receptor antagonistic activity in vitro assay on guinea pig ileumMore data for this Ligand-Target Pair
TargetSphingosine kinase 2(Mouse)
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Affinity DataKi: 1.00E+3nMAssay Description:Functional Histamine H3 receptor antagonistic activity in vitro assay on guinea pig ileumMore data for this Ligand-Target Pair
TargetSphingosine kinase 2(Human)
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Affinity DataKi: 1.30E+3nMAssay Description:Functional H2 receptor antagonistic activity in vitro assay on the isolated spontaneously beating guinea-pig right atriumMore data for this Ligand-Target Pair
TargetSphingosine kinase 1(Human)
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Affinity DataKi: 3.00E+3nMAssay Description:Antagonistic activity against (-)-noradrenaline-induced contraction of rat prostatic vas deferens (alpha1A receptor)More data for this Ligand-Target Pair
TargetSphingosine kinase 1(Human)
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Affinity DataKi: 5.00E+3nMAssay Description:Antagonistic activity against (-)-phenylephrine-induced contraction of rat spleen (Alpha-1B adrenergic receptor )More data for this Ligand-Target Pair
TargetSphingosine kinase 2(Human)
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Affinity DataKi: 6.90E+3nMAssay Description:Antagonistic activity against (-)-noradrenaline-induced contraction of rat thoracic aorta (Alpha-1D adrenergic receptor)More data for this Ligand-Target Pair
TargetSphingosine kinase 2(Human)
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Affinity DataKi: 8.00E+3nMAssay Description:Functional H2 receptor antagonistic activity in vitro assay on the isolated spontaneously beating guinea-pig right atriumMore data for this Ligand-Target Pair
TargetSphingosine kinase 2(Human)
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Affinity DataKi: 9.80E+3nMAssay Description:Functional Histamine H3 receptor antagonistic activity in vitro assay on guinea pig ileumMore data for this Ligand-Target Pair
TargetSphingosine kinase 1(Human)
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Affinity DataKi: 1.20E+4nMAssay Description:Functional Histamine H1 receptor antagonistic activity in vitro assay on guinea pig ileumMore data for this Ligand-Target Pair
TargetSphingosine kinase 2(Human)
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Affinity DataKi: 1.20E+4nMAssay Description:Functional H2 receptor antagonistic activity in vitro assay on the isolated spontaneously beating guinea-pig right atriumMore data for this Ligand-Target Pair
TargetSphingosine kinase 1(Human)
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Affinity DataKi: 1.60E+4nMAssay Description:Antagonistic activity against (-)-noradrenaline-induced contraction of rat thoracic aorta (Alpha-1D adrenergic receptor)More data for this Ligand-Target Pair
TargetSphingosine kinase 1(Mouse)
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Affinity DataKi: >2.00E+4nMAssay Description:Functional H2 receptor antagonistic activity in vitro assay on the isolated spontaneously beating guinea-pig right atriumMore data for this Ligand-Target Pair
TargetSphingosine kinase 1(Mouse)
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Affinity DataKi: 2.00E+4nMAssay Description:Functional Histamine H3 receptor antagonistic activity in vitro assay on guinea pig ileumMore data for this Ligand-Target Pair
TargetSphingosine kinase 1(Human)
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Shandong First Medical University & Shandong Academy of Medical Sciences
Curated by ChEMBL
Affinity DataKi: 2.70E+4nMAssay Description:Antagonistic activity against (-)-noradrenaline-induced contraction of rat thoracic aorta (Alpha-1D adrenergic receptor)More data for this Ligand-Target Pair
Affinity DataIC50: 0.600nMAssay Description:Antagonist activity at human delta opioid receptor expressed in CHO membrane assessed as inhibition of SNC80-induced [35S]GTPgammaS bindingMore data for this Ligand-Target Pair
Affinity DataIC50: 0.800nMAssay Description:Inhibition of recombinant ALK (unknown origin) using poly (Glu, Tyr)4:1 substrate incubated for 60 mins by ELISAMore data for this Ligand-Target Pair
Affinity DataIC50: 0.900nMAssay Description:Inhibition of recombinant ALK (unknown origin) using poly (Glu, Tyr)4:1 substrate incubated for 60 mins by ELISAMore data for this Ligand-Target Pair