Benzhydrocodone Hydrochloride
The hydrochloride salt of benzhydrocodone, a hydrocodone prodrug that releases the active opioid analgesic after oral ingestion and metabolic cleavage. The formulation is designed to reduce the potential for misuse.
Peso molecular
439,9000 g/mol
TPSA
48,00 Ų
Mecanismo de acción
Binds to mu (μ), kappa (κ), and/or delta (δ) opioid receptors in the central and peripheral nervous system, mimicking endogenous endorphins. Activation of these G-protein-coupled receptors inhibits pain signal transmission and modulates the emotional response to pain.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Binds to mu (μ), kappa (κ), and/or delta (δ) opioid receptors in the central and peripheral nervous system, mimicking endogenous endorphins. Activation of these G-protein-coupled receptors inhibits pain signal transmission …
Estructura 2D
Cite this structure
Embed this structure
SMILES
COc1ccc2c3c1O[C@H]1C(OC(=O)c4ccccc4)=CC[C@@H]4[C@@H](C2)N(C)CC[C@@]341.Cl
InChI
InChI=1S/C25H25NO4.ClH/c1-26-13-12-25-17-9-11-20(29-24(27)15-6-4-3-5-7-15)23(25)30-22-19(28-2)10-8-16(21(22)25)14-18(17)26;/h3-8,10-11,17-18,23H,9,12-14H2,1-2H3;1H/t17-,18-,23+,25+;/m1./s1
Molecular Formula
C25H26ClNO4
HBD / HBA
1 / 5
Enlaces Rotables
4
Átomos Pesados
31
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Preguntas frecuentes
The hydrochloride salt of benzhydrocodone, a hydrocodone prodrug that releases the active opioid analgesic after oral ingestion and metabolic cleavage. The formulation is designed to reduce the potential for misuse.
Binds to mu (μ), kappa (κ), and/or delta (δ) opioid receptors in the central and peripheral nervous system, mimicking endogenous endorphins. Activation of these G-protein-coupled receptors inhibits pain signal transmission and modulates the emotional response to pain.
Yes, Benzhydrocodone Hydrochloride is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL3137310. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 72736244. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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