2-Me-PVP: Difference between revisions

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{{Short description|A synthetic stimulant of the pyrrolidine class}}
== 2-Me-PVP ==
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'''2-Me-PVP''' (2-methyl-_-pyrrolidinopropiophenone) is a synthetic stimulant of the [[pyrrolidine]] class. It is chemically related to other compounds such as [[_-PVP]] and [[MDPV]].
[[File:2Me-PVP_structure.png|thumb|right|Chemical structure of 2-Me-PVP]]


==Chemical structure and properties==
'''2-Me-PVP''' (2-Methyl-_-pyrrolidinopropiophenone) is a synthetic stimulant of the [[cathinone]] class. It is chemically related to [[_-PVP]] (alpha-Pyrrolidinopentiophenone) and is known for its psychoactive effects. This compound has been used in scientific research and has also appeared in the recreational drug market.
2-Me-PVP is a derivative of [[_-PVP]], where a methyl group is added to the pyrrolidine ring. This modification results in changes to its pharmacological properties. The chemical structure of 2-Me-PVP includes a phenyl ring, a pyrrolidine ring, and a ketone group, which are characteristic of the [[cathinone]] class of compounds.


==Pharmacology==
=== Chemical Properties ===
2-Me-PVP acts as a [[stimulant]] by inhibiting the reuptake of [[dopamine]] and [[norepinephrine]], leading to increased concentrations of these neurotransmitters in the synaptic cleft. This action is similar to that of other pyrrolidine derivatives, which are known for their potent stimulant effects.
2-Me-PVP is a derivative of [[pyrrolidinophenone]], characterized by the presence of a pyrrolidine ring attached to the ketone moiety. The "2-Me" prefix indicates the presence of a methyl group at the second position of the pyrrolidine ring, which distinguishes it from other similar compounds.


==Effects==
=== Pharmacology ===
The effects of 2-Me-PVP are similar to those of other synthetic stimulants. Users may experience increased alertness, euphoria, and enhanced cognitive function. However, these effects are often accompanied by adverse reactions such as anxiety, paranoia, and cardiovascular issues.
2-Me-PVP acts as a [[central nervous system]] stimulant. It is believed to exert its effects by inhibiting the reuptake of [[dopamine]] and [[norepinephrine]], leading to increased concentrations of these neurotransmitters in the synaptic cleft. This mechanism is similar to that of other stimulants such as [[amphetamine]] and [[methylphenidate]].


==Legal status==
=== Effects ===
The legal status of 2-Me-PVP varies by country. In some jurisdictions, it is classified as a controlled substance due to its potential for abuse and lack of medical use. It is important to consult local regulations to determine its legal status.
The effects of 2-Me-PVP are reported to include increased alertness, euphoria, and enhanced cognitive function. However, it can also cause adverse effects such as anxiety, paranoia, and cardiovascular issues. The intensity and duration of these effects can vary depending on the dose and route of administration.


==Safety and toxicity==
=== Legal Status ===
The safety profile of 2-Me-PVP is not well-established, and its use is associated with significant risks. Potential adverse effects include [[tachycardia]], [[hypertension]], and [[psychosis]]. Long-term use may lead to dependence and other health complications.
The legal status of 2-Me-PVP varies by country. In some jurisdictions, it is classified as a controlled substance due to its potential for abuse and lack of medical use. In others, it may be unregulated or fall under analogue laws that control substances similar to those already banned.


==Related compounds==
=== Synthesis ===
* [[_-PVP]]
The synthesis of 2-Me-PVP involves the reaction of a propiophenone derivative with a pyrrolidine compound. The process typically requires careful control of reaction conditions to ensure the correct substitution pattern on the pyrrolidine ring.
* [[MDPV]]
* [[Methcathinone]]
* [[Pyrovalerone]]


==Related pages==
== Related Pages ==
* [[Cathinone]]
* [[Stimulant]]
* [[Stimulant]]
* [[Pyrrolidine]]
* [[_-PVP]]
* [[Cathinone]]
* [[Dopamine]]
* [[Norepinephrine]]


[[Category:Cathinones]]
[[Category:Stimulants]]
[[Category:Stimulants]]
[[Category:Pyrrolidines]]
[[Category:Synthetic drugs]]

Latest revision as of 10:47, 15 February 2025

2-Me-PVP[edit]

Chemical structure of 2-Me-PVP

2-Me-PVP (2-Methyl-_-pyrrolidinopropiophenone) is a synthetic stimulant of the cathinone class. It is chemically related to _-PVP (alpha-Pyrrolidinopentiophenone) and is known for its psychoactive effects. This compound has been used in scientific research and has also appeared in the recreational drug market.

Chemical Properties[edit]

2-Me-PVP is a derivative of pyrrolidinophenone, characterized by the presence of a pyrrolidine ring attached to the ketone moiety. The "2-Me" prefix indicates the presence of a methyl group at the second position of the pyrrolidine ring, which distinguishes it from other similar compounds.

Pharmacology[edit]

2-Me-PVP acts as a central nervous system stimulant. It is believed to exert its effects by inhibiting the reuptake of dopamine and norepinephrine, leading to increased concentrations of these neurotransmitters in the synaptic cleft. This mechanism is similar to that of other stimulants such as amphetamine and methylphenidate.

Effects[edit]

The effects of 2-Me-PVP are reported to include increased alertness, euphoria, and enhanced cognitive function. However, it can also cause adverse effects such as anxiety, paranoia, and cardiovascular issues. The intensity and duration of these effects can vary depending on the dose and route of administration.

Legal Status[edit]

The legal status of 2-Me-PVP varies by country. In some jurisdictions, it is classified as a controlled substance due to its potential for abuse and lack of medical use. In others, it may be unregulated or fall under analogue laws that control substances similar to those already banned.

Synthesis[edit]

The synthesis of 2-Me-PVP involves the reaction of a propiophenone derivative with a pyrrolidine compound. The process typically requires careful control of reaction conditions to ensure the correct substitution pattern on the pyrrolidine ring.

Related Pages[edit]