BDBM50121662 CHEMBL3616881
SMILES C[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)CC1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2CC1C(=O)N[C@@H](CCCNC(N)=N)C(O)=O
InChI Key InChIKey=PSFLEBIVFDMOMW-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 6 hits for monomerid = 50121662
Affinity DataIC50: 1.70nMAssay Description:Antagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced responseMore data for this Ligand-Target Pair
Affinity DataKi: 10nMAssay Description:Displacement of [3H]DAMGO from rat mu opiod receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 23nMAssay Description:Displacement of [3H]DAMGO from rat mu opiod receptorMore data for this Ligand-Target Pair
Affinity DataKi: 1.70E+3nMAssay Description:Displacement of [3H]DPDPE from human delta opiod receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 4.17E+3nMAssay Description:Displacement of [3H]DPDPE from human delta opiod receptorMore data for this Ligand-Target Pair
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]BK from B2R in rat brain membranes by liquid scintillation counting in based radioligand competition assayMore data for this Ligand-Target Pair
