CHEMBL217692


SMILES CC(=O)N[C@@H](C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](CN[C@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O)[C@@H](C)O)C(C)C
InChIKey YCQSOBVMPTYRFR-MLVIUDRXSA-N

Chemical properties

Hydrogen bond acceptors 26
Hydrogen bond donors 29
Rotatable bonds 63
Molecular weight (Da) 1916.1

Drug properties

Molecular type Small molecule
Endogenous/Surrogate Surrogate
Approved drug No

Database connections

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
Y2 Q9ERC0 Rat Neuropeptide Y A pIC50 7.92 7.92 7.92 ChEMBL
Y1 NPY1R Human Neuropeptide Y A pIC50 5.8 5.8 5.8 ChEMBL
Y2 NPY2R Human Neuropeptide Y A pIC50 6.98 6.98 6.98 ChEMBL