BDBM50151290 CHEMBL3770289
SMILES [H]C(NC(=O)CNC(=O)CC(CCC(O)=O)NC(=O)C(C)NC(=O)C(N)Cc1cnc[nH]1)(C(C)O)C(=O)NC(Cc1ccccc1)C(=O)NC([H])(C(C)O)C(=O)NC(CO)C(=O)NC(CC(O)=O)C(=O)NC(C(C)C)C(=O)NC(CO)C(=O)NC(CO)C(=O)NC(Cc1ccc(O)cc1)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NCC(=O)NC(CCC(N)=O)C(=O)NC(C)C(=O)NC(C)C(=O)NC(CCCCN)C(=O)NC(CCC(O)=O)C(=O)NC(Cc1ccccc1)C(=O)NC([H])(C(C)CC)C(=O)NC(C)C(=O)NC(Cc1c[nH]c2ccccc12)C(=O)NC(CC(C)C)C(=O)NC(C(C)C)C(=O)NC(CCCCN)C(=O)NCC(=O)NC(CCCNC(N)=N)C(N)=O
InChI Key InChIKey=WABVYQCWIVRVJM-YLWONWQXSA-N
Data 1 EC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 1 hit for monomerid = 50151290
Affinity DataEC50: >1.00E+3nMAssay Description:Activation of human GLP1R expressed in HEK293 cells preincubated for 30 mins followed by addition of cAMP-d2 conjugate/cryptate conjugate incubated f...More data for this Ligand-Target Pair