6,7-benzomorphans
6,7-Benzomorphan derivatives are a class of synthetic opioids that exhibit significant analgesic properties while retaining structural features reminiscent of natural morphine. These compounds typically feature a benzene ring fused to a 6,7-fused piperidine ring, conferring their distinct pharmacological profile. Notably, 6,7-Benzomorphan derivatives often possess a broader therapeutic window compared to traditional opioids, offering potential for pain management with reduced risk of respiratory depression and addiction.
These drugs are synthesized through complex organic reactions, including Friedel-Crafts alkylation, amidation, and other chemical transformations. The structural diversity within this class allows for the optimization of various properties such as potency, selectivity, and tolerability. Due to their analgesic efficacy and potential in overcoming limitations associated with traditional opioids, 6,7-Benzomorphan derivatives represent a promising area of research in pharmaceuticals and pain management.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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2,6-Methano-3-benzazocin-1-ol,1,2,3,4,5,6-hexahydro-3,6-dimethyl- | 101771-74-8 | C14H19NO |
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Opioid receptor modulator 1 | 77514-44-4 | |
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1,2,3,4,5,6-Hexahydro-2,6-methano-3-benzazocine | 575-19-9 | C12H15N |
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