BDBM50511372 CHEMBL4450693
SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCNC(=N)NC(=O)NCCCCc1cn(CCCNC(=O)CCCCCN2\C(=C\C=C\C=C\C3=[N+](C)c4ccc5c(cc(cc5c4C3(C)C)S(O)(=O)=O)S([O-])(=O)=O)C(C)(C)c3c2ccc2c(cc(cc32)S(O)(=O)=O)S(O)(=O)=O)nn1)NC(C)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O
InChI Key InChIKey=YLKYYVQJZJRLGX-UHFFFAOYSA-N
Data 2 KI
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 50511372
Affinity DataKi: 32nMAssay Description:Displacement of [3H]UR-KK200 from human Y4R expressed in CHO cells incubated for 90 mins by microbeta scintillation counting methodMore data for this Ligand-Target Pair
Affinity DataKi: 33nMAssay Description:Displacement of [3H]UR-KK200 from human Y4R expressed in CHO cells incubated for 90 mins by microbeta scintillation counting methodMore data for this Ligand-Target Pair
