BU72
Opioid analgesic drug
From Wikipedia, the free encyclopedia
BU72 is an extremely potent opioid used in pharmacological research.
| Identifiers | |
|---|---|
| |
| CAS Number | |
| PubChem CID | |
| IUPHAR/BPS | |
| ChemSpider | |
| UNII | |
| ChEMBL | |
| PDB ligand | |
| Chemical and physical data | |
| Formula | C28H32N2O2 |
| Molar mass | 428.576 g·mol−1 |
| 3D model (JSmol) | |
| |
| |
Pharmacology
BU72 is an agonist for the μ-opioid receptor with exceptionally high binding affinity and potency, comparable to carfentanil.[1] It also has extremely high efficacy, giving a stronger maximal effect than the standard full agonist DAMGO.[2] In animal studies, it was found to be a potent analgesic (giving pain relief at very low doses), with a slow onset and long duration of action.[3][4]
BU72 was used to produce the first crystal structure of the active μ-opioid receptor,[1] and is now widely used to model the activation process.[5][6][7] In the crystal structure, BU72 appears to bond to the receptor covalently,[8][9] but this seems to be an experimental artifact, since the compound binds reversibly, and preventing bond formation has no effect on affinity.[1]
Chemistry

BU72 is synthesized in several steps from thebaine.[10] Its stereochemistry has recently been revised, with the phenyl group in the (R) configuration.[11][12]