2F-QMPSB: Difference between revisions

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{{Short description|Synthetic cannabinoid}}
== 2F-QMPSB ==
{{Drugbox
| verifiedfields = changed
| verifiedrevid = 477002547
| IUPAC_name = (1-(4-fluorobutyl)-1H-indol-3-yl)(naphthalen-1-yl)methanone
| image = 2F-QMPSB_structure.png
| image_size = 200px
}}


'''2F-QMPSB''' is a synthetic cannabinoid that has been used in scientific research. It is a potent agonist of the [[cannabinoid receptor]]s, which are part of the [[endocannabinoid system]].
[[File:2F-QMPSB_structure.png|thumb|right|Chemical structure of 2F-QMPSB]]


==Chemical structure==
'''2F-QMPSB''' is a synthetic compound that belongs to the class of [[synthetic cannabinoids]]. These compounds are designed to mimic the effects of [[tetrahydrocannabinol]] (THC), the primary psychoactive component of [[cannabis]]. 2F-QMPSB is part of a larger group of substances known as [[designer drugs]], which are often created to circumvent drug laws.
2F-QMPSB belongs to the class of synthetic cannabinoids known as indole-3-carboxamides. Its chemical structure includes a fluorobutyl group attached to the indole core, which is a common feature in many synthetic cannabinoids. The presence of the fluorine atom is thought to influence the compound's binding affinity and metabolic stability.


==Pharmacology==
== Chemical Structure and Properties ==
2F-QMPSB acts as a full agonist at the [[CB1 receptor|CB1]] and [[CB2 receptor|CB2]] cannabinoid receptors. These receptors are part of the [[G protein-coupled receptor]] family and are involved in a variety of physiological processes, including pain sensation, mood regulation, and appetite control.


===Mechanism of action===
2F-QMPSB is chemically related to other synthetic cannabinoids, featuring a core structure that is modified to enhance its binding affinity to the [[cannabinoid receptor]]s in the brain. The presence of a fluorine atom in its structure is a distinguishing feature, which can affect its potency and metabolic stability.
The mechanism of action of 2F-QMPSB involves the activation of cannabinoid receptors, which leads to the inhibition of adenylate cyclase and a decrease in the intracellular concentration of [[cyclic adenosine monophosphate|cAMP]]. This results in the modulation of neurotransmitter release and various downstream effects.


==Legal status==
The chemical structure of 2F-QMPSB includes a quinolinyl moiety, which is a common feature in many synthetic cannabinoids. This structure is designed to interact with the [[CB1 receptor]] and [[CB2 receptor]], which are part of the [[endocannabinoid system]].
The legal status of 2F-QMPSB varies by country. In some jurisdictions, it is classified as a controlled substance due to its potential for abuse and lack of medical use. Researchers must comply with local regulations when handling this compound.


==Safety and toxicity==
== Pharmacology ==
As with many synthetic cannabinoids, the safety profile of 2F-QMPSB is not well-established. It is important for researchers to exercise caution and use appropriate safety measures when working with this compound. Potential adverse effects may include [[tachycardia]], [[hypertension]], and [[psychosis]].
 
2F-QMPSB acts as a potent agonist at the cannabinoid receptors, primarily the CB1 receptor, which is responsible for the psychoactive effects associated with cannabis use. The activation of these receptors by 2F-QMPSB can lead to effects such as euphoria, altered perception, and relaxation. However, due to its synthetic nature, the effects can be unpredictable and may include severe adverse reactions.
 
== Legal Status ==
 
The legal status of 2F-QMPSB varies by country. In many jurisdictions, it is classified as a controlled substance due to its potential for abuse and lack of medical use. The compound is often included in legislation targeting synthetic cannabinoids and other designer drugs.
 
== Health Risks and Concerns ==
 
The use of 2F-QMPSB is associated with significant health risks. Users may experience a range of adverse effects, including [[tachycardia]], [[hypertension]], [[anxiety]], [[paranoia]], and [[hallucinations]]. In severe cases, use can lead to [[seizures]], [[psychosis]], and even [[death]]. The variability in potency and purity of synthetic cannabinoids like 2F-QMPSB further complicates their safety profile.
 
== Related Pages ==


==Related pages==
* [[Synthetic cannabinoids]]
* [[Synthetic cannabinoids]]
* [[Cannabinoid receptor]]
* [[Cannabinoid receptor]]
* [[Designer drugs]]
* [[Endocannabinoid system]]
* [[Endocannabinoid system]]
* [[G protein-coupled receptor]]
==Gallery==
<gallery>
File:2F-QMPSB_structure.png|Chemical structure of 2F-QMPSB
</gallery>


[[Category:Synthetic cannabinoids]]
[[Category:Synthetic cannabinoids]]

Latest revision as of 10:51, 15 February 2025

2F-QMPSB[edit]

Chemical structure of 2F-QMPSB

2F-QMPSB is a synthetic compound that belongs to the class of synthetic cannabinoids. These compounds are designed to mimic the effects of tetrahydrocannabinol (THC), the primary psychoactive component of cannabis. 2F-QMPSB is part of a larger group of substances known as designer drugs, which are often created to circumvent drug laws.

Chemical Structure and Properties[edit]

2F-QMPSB is chemically related to other synthetic cannabinoids, featuring a core structure that is modified to enhance its binding affinity to the cannabinoid receptors in the brain. The presence of a fluorine atom in its structure is a distinguishing feature, which can affect its potency and metabolic stability.

The chemical structure of 2F-QMPSB includes a quinolinyl moiety, which is a common feature in many synthetic cannabinoids. This structure is designed to interact with the CB1 receptor and CB2 receptor, which are part of the endocannabinoid system.

Pharmacology[edit]

2F-QMPSB acts as a potent agonist at the cannabinoid receptors, primarily the CB1 receptor, which is responsible for the psychoactive effects associated with cannabis use. The activation of these receptors by 2F-QMPSB can lead to effects such as euphoria, altered perception, and relaxation. However, due to its synthetic nature, the effects can be unpredictable and may include severe adverse reactions.

Legal Status[edit]

The legal status of 2F-QMPSB varies by country. In many jurisdictions, it is classified as a controlled substance due to its potential for abuse and lack of medical use. The compound is often included in legislation targeting synthetic cannabinoids and other designer drugs.

Health Risks and Concerns[edit]

The use of 2F-QMPSB is associated with significant health risks. Users may experience a range of adverse effects, including tachycardia, hypertension, anxiety, paranoia, and hallucinations. In severe cases, use can lead to seizures, psychosis, and even death. The variability in potency and purity of synthetic cannabinoids like 2F-QMPSB further complicates their safety profile.

Related Pages[edit]