BDBM50587443 CHEMBL5079807
SMILES CC[C@@H](C)[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCn2nncc2COC[C@H](NC1=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N1CCC[C@H]1C(C)N1CCC[C@H]1C(N)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC1=NCN=C1)NC(=O)[C@H](Cc1ccccc1)NC(C)=O
InChI Key InChIKey=IKQOWLZHFWPKEP-UHFFFAOYSA-N
Data 2 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 50587443
Affinity DataIC50: 8.60E+3nMAssay Description:Inhibition of alexa fluor 647-labeled kinase tracer 314 binding to biotinylated-KRAS G12V mutant (unknown origin) measured after 60 mins by HTRF comp...More data for this Ligand-Target Pair
Affinity DataIC50: 8.51E+3nMAssay Description:Inhibition of alexa fluor 647-labeled kinase tracer 314 binding to biotinylated-KRAS G12V mutant (unknown origin) measured after 60 mins by HTRF comp...More data for this Ligand-Target Pair