3-quinuclidinyl benzilate

From WikiMD's Wellness Encyclopedia

3-quinuclidinyl benzilate


3-Quinuclidinyl benzilate (QNB or BZ) is a potent psychoactive drug and chemical warfare agent classified as an anticholinergic compound. It was developed in the 1950s during the Cold War for military applications, including as a non-lethal incapacitating agent. Due to its high potency and psychoactive effects, BZ has been studied extensively in both military and medical contexts.

Chemistry[edit | edit source]

3-Quinuclidinyl benzilate is a synthetic compound that belongs to the benzilate esters family. Its chemical structure consists of a quinuclidine moiety linked to a benzilic acid. This structure is responsible for its anticholinergic activity, as it acts as a competitive antagonist at muscarinic acetylcholine receptors (mAChRs) in the central and peripheral nervous system.

Pharmacology[edit | edit source]

The primary mechanism of action of BZ is the inhibition of acetylcholine (ACh) by competing with it for binding sites on mAChRs. This blockade leads to a wide range of anticholinergic symptoms, including dilated pupils (mydriasis), dry mouth (xerostomia), blurred vision, urinary retention, and, at higher doses, delirium, hallucinations, and incapacitation. The effects of BZ can last for several days, making it a powerful incapacitating agent.

Military Use[edit | edit source]

During the Cold War, BZ was developed and stockpiled by various countries as a chemical warfare agent. Its intended use was as a non-lethal incapacitating agent to temporarily disable enemy forces without causing permanent harm. However, due to its unpredictable effects and the potential for long-term psychological impact, its operational use has been limited and controversial. The Chemical Weapons Convention (CWC), which came into effect in 1997, now prohibits the production, stockpiling, and use of chemical weapons like BZ.

Medical Research[edit | edit source]

In addition to its military applications, BZ has been the subject of medical research, particularly in the study of the central nervous system and disorders related to acetylcholine dysfunction. Its potent anticholinergic properties make it a useful tool in experimental pharmacology for understanding the role of mAChRs in cognition, memory, and behavior. However, due to its high toxicity and potential for severe side effects, its use in humans is highly restricted.

Safety and Toxicology[edit | edit source]

The safety profile of 3-Quinuclidinyl benzilate is a concern due to its high potency and the severity of its anticholinergic effects. Exposure to BZ can lead to a range of adverse health effects, from mild anticholinergic symptoms to severe and potentially life-threatening delirium and psychosis. Treatment of BZ exposure focuses on supportive care and the administration of anticholinesterase agents, such as physostigmine, to counteract the anticholinergic effects.

Conclusion[edit | edit source]

3-Quinuclidinyl benzilate represents a significant chapter in the history of chemical warfare and pharmacological research. While its military use is now prohibited under international law, its impact on the fields of neurology and pharmacology continues to be of interest. The study of BZ and similar compounds helps to advance our understanding of the nervous system and the complex role of neurotransmitters like acetylcholine in human health and disease.



This chemical weapon related article is a stub. You can help WikiMD by expanding it.

WikiMD
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 / Zepbound) available.
Advertise on WikiMD

WikiMD's Wellness Encyclopedia

Let Food Be Thy Medicine
Medicine Thy Food - Hippocrates

Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. 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