BDBM50137720 (1S,3aR,6aS)-2-((S)-3-Methyl-2-{(S)-3-methyl-2-[(pyrazine-2-carbonyl)-amino]-butyrylamino}-butyryl)-octahydro-cyclopenta[c]pyrrole-1-carboxylic acid (1-cyclopropylaminooxalyl-butyl)-amide::(1S,5S,6R)-2-((S)-3-Methyl-2-{(S)-3-methyl-2-[(pyrazine-2-carbonyl)-amino]-butyrylamino}-butyryl)-octahydro-cyclopenta[c]pyrrole-1-carboxylic acid (1-cyclopropylaminooxalyl-butyl)-amide::CHEMBL264623
SMILES CCCC(NC(=O)[C@@H]1[C@H]2CCC[C@H]2CN1C(=O)[C@@H](NC(=O)[C@@H](NC(=O)c1cnccn1)C(C)C)C(C)C)C(=O)C(=O)NC1CC1
InChI Key InChIKey=RJUXWBNDZWRQEF-YOAIMQRKSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 12 hits for monomerid = 50137720
Affinity DataKi: 4nMAssay Description:Inhibitory activity of the compound against cathepsin BMore data for this Ligand-Target Pair
Affinity DataKi: 12nMAssay Description:Inhibitory activity of the compound against cathepsin LMore data for this Ligand-Target Pair
Affinity DataKi: 120nMAssay Description:Binding affinity of the compound towards Protease using PNA assay in ratsMore data for this Ligand-Target Pair
Affinity DataKi: 123nMAssay Description:Cytotoxic activity in rat liver Huh-7 cellsMore data for this Ligand-Target Pair
Affinity DataKi: 123nMAssay Description:Binding affinity towards Protease using PNA assay in ratsMore data for this Ligand-Target Pair
Affinity DataKi: 583nMAssay Description:Inhibitory activity of the compound against ChymotrypsinMore data for this Ligand-Target Pair
Affinity DataKi: 683nMAssay Description:Inhibitory activity of the compound against cathepsin KMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibitory activity of the compound against Protease using replicon assay in rats at 25 microM concentrationMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+5nMAssay Description:Cytotoxic activity in rat liver Huh-7 cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 7.00E+3nMAssay Description:Inhibitory activity of the compound against Protease using replicon assay in rats at 25 microM concentrationMore data for this Ligand-Target Pair
Affinity DataIC50: 7.00E+3nMAssay Description:Cytotoxic activity in rat liver Huh-7 cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 7.00E+3nMAssay Description:Inhibitory activity of the compound against Protease using replicon assay in rats at 25 microM concentrationMore data for this Ligand-Target Pair