null
SMILES CCCc1ccccc1-c1ccc(C[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)Cc2cnc[nH]2)[C@@H](C)O)[C@@H](C)O)C(=O)N[C@@H](Cc2ccc(cc2)-c2ccccc2C)C(N)=O)cc1
InChI Key InChIKey=WOMCZZQITXORRC-LCYWNNFESA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 1 hit for monomerid = 50301945
TargetGlucagon-like peptide 1 receptor(Homo sapiens (Human))
Bristol-Myers Squibb Company Research& Development
Curated by ChEMBL
Bristol-Myers Squibb Company Research& Development
Curated by ChEMBL
Affinity DataEC50: 93nMAssay Description:Agonist activity at human GLP1R expressed in CHO cells assessed as stimulation of intracellular [3H]cAMP accumulation after 30 mins by scintillation ...More data for this Ligand-Target Pair