BDBM50620623 CHEMBL5431678
SMILES CC(=O)N[C@@H](CCCNC(N)=N)C(=O)NC[C@@H]1[C@@H](C[C@H]1c1ccccc1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)NC[C@@H]1[C@@H](C[C@H]1c1ccccc1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O
InChI Key InChIKey=HJLLLZPWRQTNTJ-UHFFFAOYSA-N
Data 4 KI
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 4 hits for monomerid = 50620623
Affinity DataKi: 340nMAssay Description:Displacement of [3H]UR-KK200 from human Y4 receptor expressed in CHO-Gqi5-mtAQE cells measured after 90 mins by MicroBeta plate counter based competi...More data for this Ligand-Target Pair
Affinity DataKi: >1.00E+3nMAssay Description:Displacement of [3H]UR-MK299 from human Y1 receptor expressed in human SK-N-MC cells measured after 90 mins by MicroBeta plate counter based competit...More data for this Ligand-Target Pair
Affinity DataKi: >1.00E+3nMAssay Description:Displacement of [3H]propionyl-pNPY from human Y5 receptor expressed in HEC-1B cells measured after 90 mins by MicroBeta plate counter based competiti...More data for this Ligand-Target Pair
Affinity DataKi: >3.00E+3nMAssay Description:Displacement of [3H]propionyl-pNPY from human Y2 receptor expressed in CHO cells measured after 90 mins by MicroBeta plate counter based competition ...More data for this Ligand-Target Pair