6-APDB

From WikiMD's Food, Medicine & Wellness Encyclopedia

4-desoxy-MDA

6-APDB (6-(2-aminopropyl)benzofuran) is a synthetic psychoactive drug and research chemical that belongs to the substituted benzofuran and amphetamine chemical classes. It is closely related to compounds such as MDMA (3,4-methylenedioxymethamphetamine), 6-APB (6-(2-aminopropyl)benzofuran), and MDA (3,4-methylenedioxyamphetamine), sharing a similar chemical structure and pharmacological effects. 6-APDB acts primarily as a serotonin, dopamine, and norepinephrine releasing agent, which contributes to its psychoactive effects.

Chemistry[edit | edit source]

6-APDB is a benzofuran derivative of amphetamine. The molecular structure of 6-APDB consists of a benzofuran ring fused to an amphetamine backbone. This structure is similar to that of MDMA, with the main difference being the absence of the methylenedioxy group found in MDMA. The presence of the benzofuran group in 6-APDB affects its pharmacological profile, potentially making it less neurotoxic than its methylenedioxy counterparts.

Pharmacology[edit | edit source]

The pharmacological action of 6-APDB involves the release of monoamine neurotransmitters. It has been shown to promote the release of serotonin, dopamine, and norepinephrine, which are key neurotransmitters involved in mood regulation, arousal, and pleasure. The increased levels of these neurotransmitters in the synaptic cleft lead to the psychoactive effects experienced by users. The exact mechanism of action of 6-APDB, like many psychoactive substances, involves complex interactions with various neurotransmitter systems and their receptors.

Effects[edit | edit source]

The effects of 6-APDB can vary depending on the dose, method of administration, individual physiology, and environmental factors. Common reported effects include:

  • Euphoria
  • Increased empathy and sociability
  • Enhanced sensory perception
  • Mild hallucinogenic effects
  • Increased energy and alertness

However, like other psychoactive substances, 6-APDB can also produce adverse effects, which may include:

  • Anxiety and paranoia
  • Nausea and vomiting
  • Increased heart rate and blood pressure
  • Dehydration and hyperthermia
  • Potential neurotoxicity

Legal Status[edit | edit source]

The legal status of 6-APDB varies from country to country. In some jurisdictions, it is a controlled substance, making its manufacture, distribution, and possession illegal. In others, it may fall under analogue acts or temporary drug scheduling provisions, intended to prevent the distribution of novel psychoactive substances. Users and researchers should be aware of the legal implications of handling 6-APDB in their respective locations.

Research and Clinical Use[edit | edit source]

As of now, 6-APDB is primarily used for research purposes, exploring its pharmacology, toxicology, and potential therapeutic applications. There is limited clinical data on 6-APDB, and it is not approved for any medical use. Research into benzofuran compounds like 6-APDB may offer insights into developing new therapeutic agents for treating various psychiatric disorders.

Conclusion[edit | edit source]

6-APDB is a psychoactive compound with effects similar to those of MDMA and other amphetamines. While it offers potential for research into psychiatric treatment, its legal status and safety profile necessitate caution. Further research is needed to fully understand its pharmacological properties, potential therapeutic benefits, and risks.


This substance-related article is a stub. You can help WikiMD by expanding it.

Wiki.png

Navigation: Wellness - Encyclopedia - Health topics - Disease Index‏‎ - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes

Search WikiMD


Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro) available.
Advertise on WikiMD

WikiMD is not a substitute for professional medical advice. See full disclaimer.

Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.


Contributors: Prab R. Tumpati, MD