Report error Found 7252 with Last Name = 'jiang' and Initial = 'x'
TargetCalcitonin gene-related peptide type 1 receptor(Human)
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Affinity DataKi: 0.00500nMAssay Description:Binding affinity to CGRP receptor (unknown origin)More data for this Ligand-Target Pair
Affinity DataKi: 0.00500nMAssay Description:Inhibition of human factor 10aMore data for this Ligand-Target Pair
TargetCalcitonin gene-related peptide type 1 receptor(Human)
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Affinity DataKi: 0.00730nMAssay Description:Binding affinity to CGRP receptor (unknown origin)More data for this Ligand-Target Pair
TargetMelatonin receptor type 1B(Human)
The First Affiliated Hospital of China Medical University
Curated by ChEMBL
The First Affiliated Hospital of China Medical University
Curated by ChEMBL
Affinity DataKi: 0.0100nMAssay Description:Binding affinity to human MT2 receptor assessed as inhibition constantMore data for this Ligand-Target Pair
TargetCalcitonin gene-related peptide type 1 receptor(Human)
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Affinity DataKi: 0.0110nMAssay Description:Binding affinity to CGRP receptor (unknown origin)More data for this Ligand-Target Pair
TargetMelatonin receptor type 1A(Human)
The First Affiliated Hospital of China Medical University
Curated by ChEMBL
The First Affiliated Hospital of China Medical University
Curated by ChEMBL
Affinity DataKi: 0.0110nMAssay Description:Binding affinity to human MT1 receptor assessed as inhibition constantMore data for this Ligand-Target Pair
TargetCalcitonin gene-related peptide type 1 receptor(Human)
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Affinity DataKi: 0.0120nMAssay Description:Binding affinity to CGRP receptor (unknown origin)More data for this Ligand-Target Pair
Affinity DataKi: 0.0130nMAssay Description:Inhibition of human factor 10aMore data for this Ligand-Target Pair
TargetCalcitonin gene-related peptide type 1 receptor(Human)
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Affinity DataKi: 0.0130nMAssay Description:Binding affinity to CGRP receptor (unknown origin)More data for this Ligand-Target Pair
TargetCalcitonin gene-related peptide type 1 receptor(Human)
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Affinity DataKi: 0.0140nMAssay Description:Displacement of [125I]CGRP from human CGRP receptor in human SK-N-MC cells measured after 2 hrs by scintillation counting analysisMore data for this Ligand-Target Pair
TargetCalcitonin gene-related peptide type 1 receptor(Human)
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Affinity DataKi: 0.0150nMAssay Description:Displacement of [125I]CGRP from human CGRP receptor in human SK-N-MC cells measured after 2 hrs by scintillation counting analysisMore data for this Ligand-Target Pair
TargetCalcitonin gene-related peptide type 1 receptor(Human)
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Affinity DataKi: 0.0150nMAssay Description:Binding affinity to CGRP receptor (unknown origin)More data for this Ligand-Target Pair
TargetCalcitonin gene-related peptide type 1 receptor(Human)
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Affinity DataEC50: 0.0170nMAssay Description:Antagonist activity at CGRP receptor in human SK-N-MC cells assessed as inhibition of CCRP-induced cAMP productionMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 3-kinase catalytic subunit type 3(Human)
China Pharmaceutical University
Curated by ChEMBL
China Pharmaceutical University
Curated by ChEMBL
Affinity DataIC50: 0.0180nMAssay Description:Inhibition of Vps34 (unknown origin)More data for this Ligand-Target Pair
TargetCalcitonin gene-related peptide type 1 receptor(Human)
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Affinity DataKi: 0.0190nMAssay Description:Displacement of [125I]CGRP from human CGRP receptor in human SK-N-MC cells measured after 2 hrs by scintillation counting analysisMore data for this Ligand-Target Pair
TargetCalcitonin gene-related peptide type 1 receptor(Human)
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Affinity DataKi: 0.0200nMAssay Description:Displacement of [125I]CGRP from human CGRP receptor in human SK-N-MC cells measured after 2 hrs by scintillation counting analysisMore data for this Ligand-Target Pair
TargetMelatonin receptor type 1B(Human)
The First Affiliated Hospital of China Medical University
Curated by ChEMBL
The First Affiliated Hospital of China Medical University
Curated by ChEMBL
Affinity DataKi: 0.0200nMAssay Description:Binding affinity to human MT2 receptor assessed as inhibition constantMore data for this Ligand-Target Pair
TargetCalcitonin gene-related peptide type 1 receptor(Human)
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Affinity DataKi: 0.0230nMAssay Description:Binding affinity to CGRP receptor (unknown origin)More data for this Ligand-Target Pair
TargetCalcitonin gene-related peptide type 1 receptor(Human)
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Affinity DataKi: 0.0260nMAssay Description:Displacement of [125I]CGRP from human CGRP receptor in human SK-N-MC cells measured after 2 hrs by scintillation counting analysisMore data for this Ligand-Target Pair
Affinity DataKi: 0.0280nMAssay Description:Inhibition of human factor 10aMore data for this Ligand-Target Pair
TargetCalcitonin gene-related peptide type 1 receptor(Human)
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Affinity DataKi: 0.0320nMAssay Description:Binding affinity to CGRP receptor (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 0.0340nMAssay Description:Btk kinase activity was measured in vitro using an electrophoretic mobility shift assay (MSA). The ability of Btk to phosphorylate a fluorescent pept...More data for this Ligand-Target Pair
Affinity DataIC50: 0.0340nMAssay Description:Btk kinase activity was measured in vitro using an electrophoretic mobility shift assay (MSA). The ability of Btk to phosphorylate a fluorescent pept...More data for this Ligand-Target Pair
Affinity DataIC50: 0.0340nMAssay Description:Specifically the following was added: (1) compound buffer or control: 5 μL of 5× compound buffer [(5× compound buffer comprised of: 1× Master Buffer,...More data for this Ligand-Target Pair
TargetVascular endothelial growth factor receptor 2(Human)
Shenyang Pharmaceutical University
Curated by ChEMBL
Shenyang Pharmaceutical University
Curated by ChEMBL
Affinity DataIC50: 0.0350nMAssay Description:Inhibition of human VEGFR-2 using poly(Glu, Tyr) as substrate by AlphaScreen assayMore data for this Ligand-Target Pair
Affinity DataIC50: 0.0360nMAssay Description:Btk kinase activity was measured in vitro using an electrophoretic mobility shift assay (MSA). The ability of Btk to phosphorylate a fluorescent pept...More data for this Ligand-Target Pair
Affinity DataIC50: 0.0360nMAssay Description:Specifically the following was added: (1) compound buffer or control: 5 μL of 5× compound buffer [(5× compound buffer comprised of: 1× Master Buffer,...More data for this Ligand-Target Pair
TargetMelatonin receptor type 1A(Human)
The First Affiliated Hospital of China Medical University
Curated by ChEMBL
The First Affiliated Hospital of China Medical University
Curated by ChEMBL
Affinity DataKi: 0.0360nMAssay Description:Binding affinity to MT1 receptor (unknown origin) expressed in HEK293 cells assessed as inhibition constantMore data for this Ligand-Target Pair
Affinity DataIC50: 0.0360nMAssay Description:Btk kinase activity was measured in vitro using an electrophoretic mobility shift assay (MSA). The ability of Btk to phosphorylate a fluorescent pept...More data for this Ligand-Target Pair
TargetMelatonin receptor type 1B(Human)
The First Affiliated Hospital of China Medical University
Curated by ChEMBL
The First Affiliated Hospital of China Medical University
Curated by ChEMBL
Affinity DataKi: 0.0360nMAssay Description:Binding affinity to MT2 receptor (unknown origin) expressed in HEK293 cells assessed as inhibition constantMore data for this Ligand-Target Pair
TargetCalcitonin gene-related peptide type 1 receptor(Human)
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Affinity DataKi: 0.0390nMAssay Description:Binding affinity to CGRP receptor (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 0.0400nMAssay Description:Btk kinase activity was measured in vitro using an electrophoretic mobility shift assay (MSA). The ability of Btk to phosphorylate a fluorescent pept...More data for this Ligand-Target Pair
Affinity DataIC50: 0.0400nMAssay Description:Specifically the following was added: (1) compound buffer or control: 5 μL of 5× compound buffer [(5× compound buffer comprised of: 1× Master Buffer,...More data for this Ligand-Target Pair
Affinity DataIC50: 0.0400nMAssay Description:Btk kinase activity was measured in vitro using an electrophoretic mobility shift assay (MSA). The ability of Btk to phosphorylate a fluorescent pept...More data for this Ligand-Target Pair
TargetCalcitonin gene-related peptide type 1 receptor(Human)
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Affinity DataKi: 0.0430nMAssay Description:Displacement of [125I]CGRP from human CGRP receptor in human SK-N-MC cells measured after 2 hrs by scintillation counting analysisMore data for this Ligand-Target Pair
TargetCalcitonin gene-related peptide type 1 receptor(Human)
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Affinity DataKi: 0.0460nMAssay Description:Displacement of [125I]CGRP from human CGRP receptor in human SK-N-MC cells measured after 2 hrs by scintillation counting analysisMore data for this Ligand-Target Pair
Affinity DataKi: 0.0470nMAssay Description:Inhibition of human factor 10aMore data for this Ligand-Target Pair
TargetCalcitonin gene-related peptide type 1 receptor(Human)
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Affinity DataKi: 0.0480nMAssay Description:Binding affinity to CGRP receptor (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 0.0500nMAssay Description:Inhibition of SCD in human HepG2 cellsMore data for this Ligand-Target Pair
TargetMelatonin receptor type 1B(Human)
The First Affiliated Hospital of China Medical University
Curated by ChEMBL
The First Affiliated Hospital of China Medical University
Curated by ChEMBL
Affinity DataKi: 0.0500nMAssay Description:Binding affinity to MT2 (unknown origin) expressed in HEK293 cells assessed as inhibition constantMore data for this Ligand-Target Pair
TargetMelatonin receptor type 1B(Human)
The First Affiliated Hospital of China Medical University
Curated by ChEMBL
The First Affiliated Hospital of China Medical University
Curated by ChEMBL
Affinity DataKi: 0.0500nMAssay Description:Binding affinity to human MT2 receptor assessed as inhibition constantMore data for this Ligand-Target Pair
TargetMelatonin receptor type 1B(Human)
The First Affiliated Hospital of China Medical University
Curated by ChEMBL
The First Affiliated Hospital of China Medical University
Curated by ChEMBL
Affinity DataKi: 0.0500nMAssay Description:Binding affinity to human MT2 receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Affinity DataIC50: 0.0530nMAssay Description:Btk kinase activity was measured in vitro using an electrophoretic mobility shift assay (MSA). The ability of Btk to phosphorylate a fluorescent pept...More data for this Ligand-Target Pair
Affinity DataIC50: 0.0530nMAssay Description:Specifically the following was added: (1) compound buffer or control: 5 μL of 5× compound buffer [(5× compound buffer comprised of: 1× Master Buffer,...More data for this Ligand-Target Pair
Affinity DataIC50: 0.0530nMAssay Description:Btk kinase activity was measured in vitro using an electrophoretic mobility shift assay (MSA). The ability of Btk to phosphorylate a fluorescent pept...More data for this Ligand-Target Pair
TargetCalcitonin gene-related peptide type 1 receptor(Human)
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Affinity DataKi: 0.0550nMAssay Description:Binding affinity to CGRP receptor (unknown origin)More data for this Ligand-Target Pair
Affinity DataKi: 0.0570nMAssay Description:Inhibition of human factor 10aMore data for this Ligand-Target Pair
TargetCalcitonin gene-related peptide type 1 receptor(Human)
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Bristol-Myers Squibb Research & Development
Curated by ChEMBL
Affinity DataIC50: 0.0600nMAssay Description:Antagonist activity against human CGRP receptor in human SK-N-MC cells assessed as inhibition of CGRP-stimulated cAMP productionMore data for this Ligand-Target Pair
Affinity DataKi: 0.0600nMAssay Description:Inhibition of human factor 10aMore data for this Ligand-Target Pair
TargetMelatonin receptor type 1B(Human)
The First Affiliated Hospital of China Medical University
Curated by ChEMBL
The First Affiliated Hospital of China Medical University
Curated by ChEMBL
Affinity DataKi: 0.0600nMAssay Description:Binding affinity to human MT2 receptor assessed as inhibition constantMore data for this Ligand-Target Pair









































