|
Name: Allylprodine
Type: Opioid analgesic
AKA: N/A
|
|
II. Natural Derivative
Synthetic substance, no natural derivative
 |
|
III. Chemical Profile (IUPAC name)
|
|
IV. History
Allylprodine, a synthetic opioid, was developed in the late 20th century. Known for its analgesic properties, it reflects the era's interest in developing new opioid compounds. Its history includes its use in research and potential issues related to opioid addiction.
|
|
V. Legal Information
Allylprodine, a synthetic opioid, is classified as a Schedule I controlled substance in the US, making it illegal. Many countries have similarly banned it due to its high potential for abuse and lack of accepted medical use. The UNODC monitors synthetic opioids, emphasizing the need for strict controls to prevent misuse and address the opioid crisis.
US Federal Schedule - I
Schedule I drugs, substances, or chemicals are defined as drugs with no currently accepted medical use and a high potential for abuse. Some examples of Schedule I drugs are: heroin, lysergic acid diethylamide (LSD), marijuana (cannabis), 3,4-methylenedioxymethamphetamine (ecstasy), methaqualone, and peyote.
Key US Federal Policies:
Controlled Substances Act. Public Law: Public Law 91-513 (text can be found on GovInfo) (https://www.dea.gov/drug-information/csa). Date enacted: October 27, 1970.
|
|
VI. Physical Effects
Allylprodine is a synthetic opioid used for pain relief. It causes sedation and respiratory depression, acting as a downer. Short-term use is effective for managing pain, but long-term use can lead to addiction, tolerance, and severe health issues. Overdose risks include fatal respiratory depression. Safe use requires strict dosing and medical supervision. Recent research explores its efficacy and compares its risks with other opioids.  |
|
VII. Psychological Effects
Allylprodine, an opioid derivative, affects mu-opioid receptors, leading to significant euphoria and sedation. Immediate effects include mood elevation and pain relief, lasting several hours. Long-term use may result in severe addiction, cognitive impairments, and mood disturbances. Research emphasizes its potency and risks of psychological dependence and cognitive effects.
 |
|
VIII. Culture
Allylprodine, an opioid analgesic, was developed as a potential pain reliever but never became widely used. Opioids have been central to pain management, with a storied history from ancient opium use to modern pharmaceuticals. Allylprodine's cultural significance lies in its representation of the broader narrative of opioid development, including issues of pain treatment, addiction, and regulatory control. While not as prominent in media or public discourse, it highlights the complexities and challenges of opioid medications in modern healthcare. Debates about its use often intersect with larger discussions about the opioid epidemic and the need for balanced pain management strategies.
 |