Isopropylphenidate: Difference between revisions
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== Isopropylphenidate == | |||
[[File:Isopropylphenidate_Structure.svg|thumb|right|Chemical structure of Isopropylphenidate]] | |||
'''Isopropylphenidate''' is a synthetic stimulant compound that belongs to the class of [[phenidate]]s. It is chemically related to [[methylphenidate]], a well-known medication used in the treatment of [[attention deficit hyperactivity disorder]] (ADHD) and [[narcolepsy]]. Isopropylphenidate is known for its potential use as a research chemical and has been studied for its effects on the central nervous system. | |||
== | == Chemical Structure and Properties == | ||
==Legal Status== | Isopropylphenidate is characterized by its chemical structure, which includes a phenethylamine core with an isopropyl ester group. This modification distinguishes it from methylphenidate, which has a methyl ester group instead. The presence of the isopropyl group affects the compound's pharmacokinetics and pharmacodynamics, potentially altering its potency and duration of action. | ||
The legal status of isopropylphenidate varies by country. In some | |||
== Pharmacology == | |||
Isopropylphenidate acts primarily as a [[dopamine reuptake inhibitor]], increasing the concentration of dopamine in the synaptic cleft by preventing its reabsorption into the presynaptic neuron. This mechanism of action is similar to that of methylphenidate, contributing to its stimulant effects. The compound may also have some activity as a [[norepinephrine reuptake inhibitor]], although its selectivity and efficacy in this regard are less well-characterized. | |||
== Effects and Uses == | |||
The effects of isopropylphenidate are similar to those of other stimulant drugs, including increased alertness, enhanced focus, and elevated mood. However, due to its status as a research chemical, it is not approved for medical use and lacks comprehensive clinical data. Its use is primarily limited to scientific research and experimentation. | |||
== Legal Status == | |||
The legal status of isopropylphenidate varies by country. In some jurisdictions, it may be classified as a controlled substance, while in others, it may be legal to possess and use for research purposes. It is important for researchers to be aware of and comply with local regulations regarding its use. | |||
== Safety and Toxicity == | |||
As with many research chemicals, the safety profile of isopropylphenidate is not well-established. Potential risks may include cardiovascular effects, neurotoxicity, and the potential for abuse and dependence. Caution is advised when handling and studying this compound. | |||
== Related Pages == | |||
* [[Methylphenidate]] | * [[Methylphenidate]] | ||
* [[ | * [[Dopamine reuptake inhibitor]] | ||
* [[ | * [[Attention deficit hyperactivity disorder]] | ||
* [[Stimulant]] | |||
{{Stimulants}} | |||
[[Category:Stimulants]] | [[Category:Stimulants]] | ||
[[Category:Research chemicals]] | [[Category:Research chemicals]] | ||
Latest revision as of 16:33, 16 February 2025
Isopropylphenidate[edit]
Isopropylphenidate is a synthetic stimulant compound that belongs to the class of phenidates. It is chemically related to methylphenidate, a well-known medication used in the treatment of attention deficit hyperactivity disorder (ADHD) and narcolepsy. Isopropylphenidate is known for its potential use as a research chemical and has been studied for its effects on the central nervous system.
Chemical Structure and Properties[edit]
Isopropylphenidate is characterized by its chemical structure, which includes a phenethylamine core with an isopropyl ester group. This modification distinguishes it from methylphenidate, which has a methyl ester group instead. The presence of the isopropyl group affects the compound's pharmacokinetics and pharmacodynamics, potentially altering its potency and duration of action.
Pharmacology[edit]
Isopropylphenidate acts primarily as a dopamine reuptake inhibitor, increasing the concentration of dopamine in the synaptic cleft by preventing its reabsorption into the presynaptic neuron. This mechanism of action is similar to that of methylphenidate, contributing to its stimulant effects. The compound may also have some activity as a norepinephrine reuptake inhibitor, although its selectivity and efficacy in this regard are less well-characterized.
Effects and Uses[edit]
The effects of isopropylphenidate are similar to those of other stimulant drugs, including increased alertness, enhanced focus, and elevated mood. However, due to its status as a research chemical, it is not approved for medical use and lacks comprehensive clinical data. Its use is primarily limited to scientific research and experimentation.
Legal Status[edit]
The legal status of isopropylphenidate varies by country. In some jurisdictions, it may be classified as a controlled substance, while in others, it may be legal to possess and use for research purposes. It is important for researchers to be aware of and comply with local regulations regarding its use.
Safety and Toxicity[edit]
As with many research chemicals, the safety profile of isopropylphenidate is not well-established. Potential risks may include cardiovascular effects, neurotoxicity, and the potential for abuse and dependence. Caution is advised when handling and studying this compound.
Related Pages[edit]
| Stimulants | ||||||||||
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