TargetMelatonin receptor type 1B(Homo sapiens (Human))
Massachusetts General Hospital
Curated by PDSP Ki Database
Massachusetts General Hospital
Curated by PDSP Ki Database
TargetMelatonin receptor type 1A(Homo sapiens (Human))
Massachusetts General Hospital
Curated by PDSP Ki Database
Massachusetts General Hospital
Curated by PDSP Ki Database
TargetMelatonin receptor type 1B(Homo sapiens (Human))
Massachusetts General Hospital
Curated by PDSP Ki Database
Massachusetts General Hospital
Curated by PDSP Ki Database
TargetMelatonin receptor type 1A(Homo sapiens (Human))
Massachusetts General Hospital
Curated by PDSP Ki Database
Massachusetts General Hospital
Curated by PDSP Ki Database
TargetMelatonin receptor type 1B(Homo sapiens (Human))
Massachusetts General Hospital
Curated by PDSP Ki Database
Massachusetts General Hospital
Curated by PDSP Ki Database
TargetMelatonin receptor type 1B(Homo sapiens (Human))
Massachusetts General Hospital
Curated by PDSP Ki Database
Massachusetts General Hospital
Curated by PDSP Ki Database
TargetMelatonin receptor type 1B(Homo sapiens (Human))
Massachusetts General Hospital
Curated by PDSP Ki Database
Massachusetts General Hospital
Curated by PDSP Ki Database
TargetMelatonin receptor type 1B(Homo sapiens (Human))
Massachusetts General Hospital
Curated by PDSP Ki Database
Massachusetts General Hospital
Curated by PDSP Ki Database
TargetMelatonin receptor type 1A(Homo sapiens (Human))
Massachusetts General Hospital
Curated by PDSP Ki Database
Massachusetts General Hospital
Curated by PDSP Ki Database
TargetMelatonin receptor type 1B(Homo sapiens (Human))
Massachusetts General Hospital
Curated by PDSP Ki Database
Massachusetts General Hospital
Curated by PDSP Ki Database
TargetMelatonin receptor type 1A(Homo sapiens (Human))
Massachusetts General Hospital
Curated by PDSP Ki Database
Massachusetts General Hospital
Curated by PDSP Ki Database
TargetMelatonin receptor type 1B(Homo sapiens (Human))
Massachusetts General Hospital
Curated by PDSP Ki Database
Massachusetts General Hospital
Curated by PDSP Ki Database
TargetMelatonin receptor type 1B(Homo sapiens (Human))
Massachusetts General Hospital
Curated by PDSP Ki Database
Massachusetts General Hospital
Curated by PDSP Ki Database
TargetMelatonin receptor type 1A(Homo sapiens (Human))
Massachusetts General Hospital
Curated by PDSP Ki Database
Massachusetts General Hospital
Curated by PDSP Ki Database
TargetMelatonin receptor type 1B(Homo sapiens (Human))
Massachusetts General Hospital
Curated by PDSP Ki Database
Massachusetts General Hospital
Curated by PDSP Ki Database
TargetMelatonin receptor type 1B(Homo sapiens (Human))
Massachusetts General Hospital
Curated by PDSP Ki Database
Massachusetts General Hospital
Curated by PDSP Ki Database
TargetMelatonin receptor type 1A(Homo sapiens (Human))
Massachusetts General Hospital
Curated by PDSP Ki Database
Massachusetts General Hospital
Curated by PDSP Ki Database
TargetMelatonin receptor type 1B(Homo sapiens (Human))
Massachusetts General Hospital
Curated by PDSP Ki Database
Massachusetts General Hospital
Curated by PDSP Ki Database
TargetMelatonin receptor type 1B(Homo sapiens (Human))
Massachusetts General Hospital
Curated by PDSP Ki Database
Massachusetts General Hospital
Curated by PDSP Ki Database
TargetMelatonin receptor type 1A(Homo sapiens (Human))
Massachusetts General Hospital
Curated by PDSP Ki Database
Massachusetts General Hospital
Curated by PDSP Ki Database
Affinity DataIC50: 1nMAssay Description:Antagonistic activity against P2X7 receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 2nMAssay Description:Binding to Estrogen receptor- beta (ER beta) receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 2nMAssay Description:Binding to Estrogen receptor- alpha (ER alpha) receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 2.30nMAssay Description:Displacement of [3H]PGD2 from human CRTh2 expressed in HEK293 cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 2.60nMAssay Description:Displacement of [3H]PGD2 from human CRTh2 expressed in HEK293 cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 5.40nMAssay Description:Displacement of [3H]PGD2 from human CRTh2 expressed in HEK293 cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 6nMAssay Description:Displacement of [3H]PGD2 from human CRTh2 expressed in HEK293 cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 7nMAssay Description:Binding to Estrogen receptor- alpha (ER alpha) receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 7.10nMAssay Description:Displacement of [3H]PGD2 from human CRTh2 expressed in HEK293 cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 8nMAssay Description:Displacement of [3H]PGD2 from human CRTh2 expressed in HEK293 cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 11nMAssay Description:Displacement of [3H]PGD2 from human CRTh2 expressed in HEK293 cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 13nMAssay Description:Antagonist activity at human FPR1 in human neutrophils assessed as inhibition of fMLF-stimulated intracellular calcium mobilisation by FLIPR assayMore data for this Ligand-Target Pair
Affinity DataIC50: 18nMAssay Description:Displacement of [3H]PGD2 from human CRTh2 expressed in HEK293 cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 18nMAssay Description:Displacement of [3H]PGD2 from human CRTh2 expressed in HEK293 cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 19.9nMAssay Description:Antagonist activity at human recombinant C5a receptor in HEK cells assessed as inhibition of C5a-induced calcium mobilizationMore data for this Ligand-Target Pair
Affinity DataIC50: 21nMAssay Description:Displacement of [3H]PGD2 from human CRTh2 expressed in HEK293 cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 23nMAssay Description:Displacement of [3H]PGD2 from human CRTh2 expressed in HEK293 cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 25nMAssay Description:Antagonist activity at human FPR1 in human neutrophils assessed as inhibition of fMLF-stimulated intracellular calcium mobilisation by FLIPR assayMore data for this Ligand-Target Pair
Affinity DataIC50: 25nMAssay Description:Antagonist activity at human FPR1 in human neutrophils assessed as inhibition of fMLF-stimulated intracellular calcium mobilisation by FLIPR assayMore data for this Ligand-Target Pair
Affinity DataIC50: 25.1nMAssay Description:Antagonist activity at human recombinant C5a receptor in HEK cells assessed as inhibition of C5a-induced calcium mobilizationMore data for this Ligand-Target Pair
Affinity DataIC50: 30nMAssay Description:Binding to Estrogen receptor- alpha (ER alpha) receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 31.6nMAssay Description:Displacement of [Alexa647]C5a from human recombinant C5a receptor expressed in HEK cells by membrane binding assay in presence of [35S]GTPgammaSMore data for this Ligand-Target Pair
Affinity DataIC50: 32nMAssay Description:Antagonist activity at rat P2X7 receptor transfected in HEK cells assessed as inhibition of benzylATP-induced changes in plasma membrane pore formati...More data for this Ligand-Target Pair
Affinity DataIC50: 32nMAssay Description:Antagonist activity at rat P2X7 receptor transfected in HEK cells assessed as inhibition of benzylATP-induced changes in plasma membrane pore formati...More data for this Ligand-Target Pair