null
SMILES COc1ccc([C@H]2[C@@H]([C@H](c3ccc(NC(C)C)nc23)c2ccc3OCOc3c2)C(O)=O)c(CC(C)C(=O)N(C)C)c1
InChI Key InChIKey=IDRPGYTWDRQQOE-NBNHAXFZSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 4 hits for monomerid = 50141468
TargetEndothelin-1 receptor(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 0.0240nMAssay Description:Inhibitory activity against [125I]-ET-1 binding to human endothelin A receptorMore data for this Ligand-Target Pair
TargetEndothelin receptor type B(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 43nMAssay Description:Inhibitory activity against [125I]-ET-1 binding to human endothelin B receptorMore data for this Ligand-Target Pair
TargetEndothelin-1 receptor(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 0.0240nMAssay Description:Inhibitory activity against [125I]-ET-1 binding to human endothelin A receptorMore data for this Ligand-Target Pair
TargetEndothelin receptor type B(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 43nMAssay Description:Inhibitory activity against [125I]-ET-1 binding to human endothelin B receptorMore data for this Ligand-Target Pair