eglumegad


SMILES OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O
InChIKey VTAARTQTOOYTES-RGDLXGNYSA-N

Chemical properties

Hydrogen bond acceptors 3
Hydrogen bond donors 3
Rotatable bonds 2
Molecular weight (Da) 185.1

Drug properties

Molecular type Small molecule
Endogenous/Surrogate Surrogate
Approved drug No

Database connections

Structure pdb 7EPB 7E9G

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
κ OPRK Human Opioid A pKi 7.1 7.1 7.1 Guide to Pharmacology
κ OPRK Rat Opioid A pKd 6.08 6.08 6.08 ChEMBL
μ OPRM Rat Opioid A pKd 8.0 8.85 9.7 ChEMBL
μ OPRM Human Opioid A pKi 8.77 8.77 8.77 PDSP Ki database
δ OPRD Human Opioid A pKi 6.69 6.69 6.69 PDSP Ki database
κ OPRK Human Opioid A pKi 7.08 7.08 7.08 PDSP Ki database
δ A0A286XTF2 Guinea pig Opioid A pKi 7.33 7.37 7.4 PDSP Ki database
δ OPRD Mouse Opioid A pKi 6.9 6.9 6.9 PDSP Ki database
μ OPRM Bovine Opioid A pKi 7.88 8.76 9.64 PDSP Ki database
δ F1N083 Bovine Opioid A pKi 6.0 6.96 7.45 PDSP Ki database
κ OPRK Guinea pig Opioid A pKi 6.74 6.92 7.1 PDSP Ki database
μ OPRM Rat Opioid A pKi 6.85 8.7 9.55 PDSP Ki database
δ OPRD Human Opioid A pKi 6.7 6.7 6.7 Guide to Pharmacology
μ OPRM Human Opioid A pKi 8.8 8.8 8.8 Guide to Pharmacology
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database