DPDPE


SMILES CC1(C(C(=O)NCC(=O)NC(C(=O)NC(C(SS1)(C)C)C(=O)O)CC2=CC=CC=C2)NC(=O)C(CC3=CC=C(C=C3)O)N)C
InChIKey MCMMCRYPQBNCPH-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 9
Hydrogen bond donors 7
Rotatable bonds 7
Molecular weight (Da) 645.2

Drug properties

Molecular type Small molecule
Physiological/Surrogate Surrogate
Approved drug No

Database connections

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
μ OPRM Mouse Opioid A pKi 7.12 7.13 7.15 PDSP Ki database
μ OPRM Human Opioid A pKi 6.37 6.37 6.37 PDSP Ki database
δ OPRD Human Opioid A pKi 7.77 8.37 9.06 PDSP Ki database
δ OPRD Mouse Opioid A pKi 8.47 8.47 8.47 PDSP Ki database
δ OPRD Rat Opioid A pKi 5.99 7.29 8.67 PDSP Ki database
μ OPRM Rat Opioid A pKi 6.42 6.42 6.42 PDSP Ki database
κ OPRK Rat Opioid A pKi 5.0 5.0 5.0 PDSP Ki database
CB1 CNR1 Human Cannabinoid A pKi 6.0 6.0 6.0 PDSP Ki database
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database