BDBM50167749 Azaline B derivative::CHEMBL411987
SMILES CC(C)C[C@H](NC(=O)[C@@H](Cc1ccc(NC(N)=O)cc1)NC(=O)[C@H](Cc1ccc(NC(=O)C(N)CCN)cc1)NC(=O)[C@H](CO)NC(=O)[C@@H](Cc1cccnc1)NC(=O)[C@@H](Cc1ccc(Cl)cc1)NC(=O)[C@@H](Cc1ccc2ccccc2c1)NC(C)=O)C(=O)N[C@@H](CCCCNC(C)C)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(O)=O
InChI Key InChIKey=MFDVHDDOBORVAZ-UHFFFAOYSA-N
Data 2 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 50167749
Affinity DataIC50: 3.20nMAssay Description:In vitro inhibition of human gonadotropin-releasing hormone expressed in HEK293 cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 3.53nMAssay Description:In vitro inhibition of human gonadotropin-releasing hormone expressed in HEK293 cellsMore data for this Ligand-Target Pair
