BU72

Opioid analgesic drug From Wikipedia, the free encyclopedia

BU72 is an extremely potent opioid used in pharmacological research.

CAS Number
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BU72
Identifiers
  • (2R,3S,3aR,5aR,6R,11bR,11cS)-3a-methoxy-3,14-dimethyl-2-phenyl-2,3,3a,6,7,11c-hexahydro-1H-6,11b-(epiminoethano)-3,5a-methanonaphtho[2,1-g]indol-10-ol
CAS Number
PubChem CID
IUPHAR/BPS
ChemSpider
UNII
ChEMBL
PDB ligand
Chemical and physical data
FormulaC28H32N2O2
Molar mass428.576 g·mol−1
3D model (JSmol)
  • CO[C@]12C=C[C@]34C[C@@]1(C)[C@H](N[C@H]2[C@@]35CCN(C)[C@@H]4Cc6ccc(O)cc56)c7ccccc7
  • InChI=InChI=1S/C28H32N2O2/c1-25-17-26-11-12-28(25,32-3)24(29-23(25)18-7-5-4-6-8-18)27(26)13-14-30(2)22(26)15-19-9-10-20(31)16-21(19)27/h4-12,16,22-24,29,31H,13-15,17H2,1-3H3/t22-,23-,24+,25+,26-,27+,28+/m1/s1
  • Key:RGJHUVJQGAAZLK-GKTFKBBASA-N
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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 original proposed structure ((S)-phenyl epimer)

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]

See also

References

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