3-Allylfentanyl
3-Allylfentanyl[edit | edit source]
3-Allylfentanyl is a synthetic opioid analgesic that is structurally related to fentanyl. It is part of the phenylpiperidine class of opioids, which are known for their potent analgesic properties. This compound is primarily of interest in the field of medicinal chemistry and pharmacology due to its potential applications in pain management and its role in the study of opioid receptor interactions.
Chemical Structure and Properties[edit | edit source]
3-Allylfentanyl is characterized by the presence of an allyl group attached to the nitrogen atom of the piperidine ring, which distinguishes it from other fentanyl analogs. The chemical structure of 3-Allylfentanyl can be represented by the molecular formula C22H28N2O. The presence of the allyl group may influence the compound's binding affinity and activity at the mu-opioid receptor.
Pharmacology[edit | edit source]
As an opioid, 3-Allylfentanyl exerts its effects primarily through agonism of the mu-opioid receptor, which is responsible for its analgesic and euphoric effects. The modification of the fentanyl structure with an allyl group may alter its pharmacokinetic and pharmacodynamic properties, potentially affecting its potency, duration of action, and side effect profile.
Synthesis[edit | edit source]
The synthesis of 3-Allylfentanyl involves the modification of the fentanyl molecule through the introduction of an allyl group. This process typically requires advanced organic synthesis techniques and a thorough understanding of the chemical reactivity of the fentanyl scaffold. The synthesis of such analogs is often conducted in research laboratories focused on the development of new analgesics.
Legal Status[edit | edit source]
Due to its structural similarity to fentanyl, 3-Allylfentanyl is likely to be regulated under similar legal frameworks as other fentanyl analogs. These compounds are often subject to strict controls due to their potential for abuse and the risk of overdose. The legal status of 3-Allylfentanyl may vary by country and is subject to change as new regulations are enacted.
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