Ciprefadol

Ciprefadol is a synthetic opioid that was developed in the late 1970s. It is a narcotic analgesic that is primarily used in the treatment of moderate to severe pain. Ciprefadol is a member of the 4-phenylpiperidine class of opioids and is closely related to the highly potent opioid analgesic, fentanyl.

Pharmacology[edit | edit source]

Ciprefadol acts as a mu-opioid receptor agonist. It has a high affinity for the mu-opioid receptor, which is the primary site of action for most opioid drugs. The activation of these receptors in the brain and spinal cord reduces the perception of pain.

Chemistry[edit | edit source]

Ciprefadol is a synthetic opioid and is part of the 4-phenylpiperidine class of opioids. It is structurally similar to other opioids in this class, such as fentanyl and sufentanil. The chemical structure of ciprefadol includes a phenyl ring attached to a piperidine ring, which is a common feature of this class of drugs.

Clinical Use[edit | edit source]

Ciprefadol is used in the treatment of moderate to severe pain. It is often used in situations where other pain medications are not effective. Due to its potency, it is typically reserved for use in patients with severe chronic pain or in those who have developed a tolerance to other opioids.

Side Effects[edit | edit source]

Like all opioids, ciprefadol has a number of potential side effects. These can include nausea, vomiting, constipation, and respiratory depression. In addition, long-term use of ciprefadol can lead to physical dependence and addiction.

See Also[edit | edit source]

Ciprefadol Resources
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