BIM 23268


SMILES CC(C1C(=O)NC(C(=O)NC(CSSCC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N1)CCCCN)CC2=CNC3=CC=CC=C32)CC4=CC=CC=C4)CC5=CC=CC=C5)N)C(=O)N)CC6=CC=CC=C6)O
InChIKey JNMPZUZCPFIJGJ-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 13
Hydrogen bond donors 12
Rotatable bonds 14
Molecular weight (Da) 1077.5

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
SST1 SSR1 Human Somatostatin A pKi 6.24 7.24 7.74 PDSP Ki database
SST2 SSR2 Human Somatostatin A pKi 7.82 7.82 7.82 PDSP Ki database
SST3 SSR3 Human Somatostatin A pKi 7.21 7.21 7.21 PDSP Ki database
SST4 SSR4 Human Somatostatin A pKi 6.76 7.45 7.79 PDSP Ki database
SST5 SSR5 Human Somatostatin A pKi 8.66 9.17 9.43 PDSP Ki database
SST5 SSR5 Rat Somatostatin A pKi 8.47 8.47 8.47 PDSP Ki database
SST2 SSR2 Rat Somatostatin A pKi 7.0 7.0 7.0 PDSP Ki database
SST3 SSR3 Rat Somatostatin A pKi 8.39 8.39 8.39 PDSP Ki database
SST2 SSR2 Mouse Somatostatin A pKi 7.96 8.39 8.83 PDSP Ki database
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database