3-Chloroamphetamine: Difference between revisions
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== 3-Chloroamphetamine == | |||
[[File:3-Chloroamphetamine.svg|thumb|right|Structural formula of 3-Chloroamphetamine]] | |||
3-Chloroamphetamine | |||
'''3-Chloroamphetamine''' (3-CA) is a [[chemical compound]] that belongs to the class of [[substituted amphetamines]]. It is a [[derivative]] of [[amphetamine]] where a [[chlorine]] atom is substituted at the third position of the phenyl ring. This compound is primarily of interest in [[neuropharmacology]] and [[toxicology]] due to its effects on the [[central nervous system]]. | |||
3-Chloroamphetamine | |||
=== | == Chemical Properties == | ||
3-Chloroamphetamine is characterized by the presence of a chlorine atom, which significantly alters its [[pharmacological]] properties compared to [[amphetamine]]. The molecular formula of 3-CA is C9H12ClN, and it has a [[molecular weight]] of 169.65 g/mol. The presence of the chlorine atom increases the [[lipophilicity]] of the compound, affecting its [[bioavailability]] and [[metabolism]]. | |||
3-Chloroamphetamine | |||
== | == Pharmacology == | ||
== | 3-Chloroamphetamine acts primarily as a [[serotonin]] [[neurotoxin]], which means it can cause damage to [[serotonergic neurons]]. It is known to deplete [[serotonin]] levels in the brain, leading to potential [[neurotoxicity]]. This property makes it a compound of interest in studying the effects of serotonin depletion and the mechanisms of [[neurodegeneration]]. | ||
=== Mechanism of Action === | |||
The mechanism by which 3-CA exerts its effects involves the inhibition of the [[serotonin transporter]] (SERT), leading to increased levels of serotonin in the [[synaptic cleft]]. However, prolonged exposure results in the depletion of serotonin and damage to serotonin-producing neurons. This is thought to occur through the generation of [[reactive oxygen species]] and other [[oxidative stress]] mechanisms. | |||
== Toxicology == | |||
Due to its neurotoxic effects, 3-Chloroamphetamine is not used therapeutically. Studies in [[animal models]] have shown that exposure to 3-CA can lead to long-term reductions in serotonin levels and damage to serotonin pathways. This has implications for understanding [[neurodegenerative diseases]] and the potential risks of exposure to similar compounds. | |||
== Synthesis == | |||
The synthesis of 3-Chloroamphetamine involves the chlorination of [[amphetamine]] or its precursors. This process requires careful control of reaction conditions to ensure the selective substitution of the chlorine atom at the desired position on the phenyl ring. | |||
== Related Compounds == | |||
3-Chloroamphetamine is related to other [[halogenated amphetamines]], such as [[4-chloroamphetamine]] and [[3,4-methylenedioxyamphetamine]] (MDA). These compounds share similar structural features but differ in their pharmacological and toxicological profiles. | |||
== Related Pages == | |||
* [[Amphetamine]] | * [[Amphetamine]] | ||
* [[Serotonin]] | * [[Serotonin]] | ||
* [[Neurotoxicity]] | * [[Neurotoxicity]] | ||
* [[Central nervous system]] | |||
[[Category:Substituted amphetamines]] | [[Category:Substituted amphetamines]] | ||
[[Category: | [[Category:Neurotoxins]] | ||
[[Category: | [[Category:Chlorine compounds]] | ||
Latest revision as of 05:22, 16 February 2025
3-Chloroamphetamine[edit]
3-Chloroamphetamine (3-CA) is a chemical compound that belongs to the class of substituted amphetamines. It is a derivative of amphetamine where a chlorine atom is substituted at the third position of the phenyl ring. This compound is primarily of interest in neuropharmacology and toxicology due to its effects on the central nervous system.
Chemical Properties[edit]
3-Chloroamphetamine is characterized by the presence of a chlorine atom, which significantly alters its pharmacological properties compared to amphetamine. The molecular formula of 3-CA is C9H12ClN, and it has a molecular weight of 169.65 g/mol. The presence of the chlorine atom increases the lipophilicity of the compound, affecting its bioavailability and metabolism.
Pharmacology[edit]
3-Chloroamphetamine acts primarily as a serotonin neurotoxin, which means it can cause damage to serotonergic neurons. It is known to deplete serotonin levels in the brain, leading to potential neurotoxicity. This property makes it a compound of interest in studying the effects of serotonin depletion and the mechanisms of neurodegeneration.
Mechanism of Action[edit]
The mechanism by which 3-CA exerts its effects involves the inhibition of the serotonin transporter (SERT), leading to increased levels of serotonin in the synaptic cleft. However, prolonged exposure results in the depletion of serotonin and damage to serotonin-producing neurons. This is thought to occur through the generation of reactive oxygen species and other oxidative stress mechanisms.
Toxicology[edit]
Due to its neurotoxic effects, 3-Chloroamphetamine is not used therapeutically. Studies in animal models have shown that exposure to 3-CA can lead to long-term reductions in serotonin levels and damage to serotonin pathways. This has implications for understanding neurodegenerative diseases and the potential risks of exposure to similar compounds.
Synthesis[edit]
The synthesis of 3-Chloroamphetamine involves the chlorination of amphetamine or its precursors. This process requires careful control of reaction conditions to ensure the selective substitution of the chlorine atom at the desired position on the phenyl ring.
Related Compounds[edit]
3-Chloroamphetamine is related to other halogenated amphetamines, such as 4-chloroamphetamine and 3,4-methylenedioxyamphetamine (MDA). These compounds share similar structural features but differ in their pharmacological and toxicological profiles.
