AP5: Difference between revisions

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{{Short description|A chemical compound used in neuroscience research}}
{{DISPLAYTITLE:AP5 (2-Amino-5-phosphonovaleric acid)}}
{{Use dmy dates|date=October 2023}}


'''AP5''' (2-Amino-5-phosphonopentanoate) is a chemical compound that acts as a selective [[NMDA receptor]] antagonist. It is commonly used in [[neuroscience]] research to study the role of NMDA receptors in synaptic plasticity and [[neurotransmission]].
== AP5 (2-Amino-5-phosphonovaleric acid) ==
[[File:AP5 2-Amino-5-phosphonovaleriansäure.svg|thumb|right|Chemical structure of AP5]]


==Chemical structure and properties==
'''AP5''', also known as '''2-Amino-5-phosphonovaleric acid''', is a chemical compound that acts as a selective [[NMDA receptor]] antagonist. It is commonly used in [[neuroscience]] research to study the role of NMDA receptors in [[synaptic plasticity]] and [[neurotransmission]].
AP5 is a derivative of [[valeric acid]], with a phosphono group attached to the fifth carbon of the pentanoic acid chain. Its chemical formula is C<sub>5</sub>H<sub>12</sub>NO<sub>5</sub>P, and it is a white crystalline powder that is soluble in water.


==Mechanism of action==
== Chemical Properties ==
AP5 functions by competitively inhibiting the binding of the neurotransmitter [[glutamate]] to NMDA receptors. This inhibition prevents the opening of the ion channel associated with the receptor, thereby blocking the influx of [[calcium ions]] (Ca<sup>2+</sup>) into the neuron. This action is crucial for studying the role of NMDA receptors in [[long-term potentiation]] (LTP) and [[long-term depression]] (LTD), which are processes involved in [[synaptic plasticity]] and memory formation.
AP5 is a [[phosphonic acid]] derivative with the chemical formula C<sub>5</sub>H<sub>12</sub>NO<sub>5</sub>P. It is a white crystalline powder that is soluble in water. The compound is characterized by the presence of an amino group and a phosphonic acid group, which are responsible for its biological activity.


==Applications in research==
== Mechanism of Action ==
AP5 is widely used in experimental settings to investigate the physiological and pathological roles of NMDA receptors. It is particularly useful in studies of [[neurodegenerative diseases]], such as [[Alzheimer's disease]], where NMDA receptor dysfunction is implicated. Additionally, AP5 is employed in research on [[epilepsy]], [[schizophrenia]], and [[chronic pain]], where altered NMDA receptor activity is observed.
AP5 functions by competitively inhibiting the binding of the neurotransmitter [[glutamate]] to the NMDA receptor. This inhibition prevents the opening of the ion channel associated with the receptor, thereby blocking the influx of [[calcium ions]] (Ca<sup>2+</sup>) into the [[neuron]]. This action is crucial for understanding the role of NMDA receptors in [[long-term potentiation]] (LTP), a cellular mechanism underlying [[learning]] and [[memory]].


==Safety and handling==
== Applications in Research ==
As with many chemical compounds used in research, AP5 should be handled with care. It is important to use appropriate [[personal protective equipment]] (PPE) and follow safety protocols to prevent exposure. AP5 should be stored in a cool, dry place, away from incompatible substances.
In [[experimental neuroscience]], AP5 is used to investigate the involvement of NMDA receptors in various physiological and pathological processes. For example, it is employed in studies of [[epilepsy]], [[ischemic brain injury]], and [[neurodegenerative diseases]] such as [[Alzheimer's disease]]. By blocking NMDA receptors, researchers can assess the contribution of these receptors to neuronal excitability and synaptic strength.


==Related pages==
== Safety and Handling ==
AP5 should be handled with care in a laboratory setting. It is important to use appropriate [[personal protective equipment]] (PPE) such as gloves and goggles when working with this compound. Although AP5 is not highly toxic, it should be used in well-ventilated areas to minimize exposure.
 
== Related Pages ==
* [[NMDA receptor]]
* [[NMDA receptor]]
* [[Glutamate (neurotransmitter)]]
* [[Glutamate]]
* [[Synaptic plasticity]]
* [[Synaptic plasticity]]
* [[Long-term potentiation]]
* [[Neurotransmission]]
* [[Neurotransmission]]
==Gallery==
<gallery>
File:2-Amino-5-phosphonovaleriansäure.svg|Chemical structure of AP5
</gallery>


[[Category:Neuroscience]]
[[Category:Neuroscience]]
[[Category:Pharmacology]]
[[Category:Pharmacology]]
[[Category:Chemical compounds]]
[[Category:Chemical compounds]]

Revision as of 11:32, 15 February 2025


AP5 (2-Amino-5-phosphonovaleric acid)

File:AP5 2-Amino-5-phosphonovaleriansäure.svg
Chemical structure of AP5

AP5, also known as 2-Amino-5-phosphonovaleric acid, is a chemical compound that acts as a selective NMDA receptor antagonist. It is commonly used in neuroscience research to study the role of NMDA receptors in synaptic plasticity and neurotransmission.

Chemical Properties

AP5 is a phosphonic acid derivative with the chemical formula C5H12NO5P. It is a white crystalline powder that is soluble in water. The compound is characterized by the presence of an amino group and a phosphonic acid group, which are responsible for its biological activity.

Mechanism of Action

AP5 functions by competitively inhibiting the binding of the neurotransmitter glutamate to the NMDA receptor. This inhibition prevents the opening of the ion channel associated with the receptor, thereby blocking the influx of calcium ions (Ca2+) into the neuron. This action is crucial for understanding the role of NMDA receptors in long-term potentiation (LTP), a cellular mechanism underlying learning and memory.

Applications in Research

In experimental neuroscience, AP5 is used to investigate the involvement of NMDA receptors in various physiological and pathological processes. For example, it is employed in studies of epilepsy, ischemic brain injury, and neurodegenerative diseases such as Alzheimer's disease. By blocking NMDA receptors, researchers can assess the contribution of these receptors to neuronal excitability and synaptic strength.

Safety and Handling

AP5 should be handled with care in a laboratory setting. It is important to use appropriate personal protective equipment (PPE) such as gloves and goggles when working with this compound. Although AP5 is not highly toxic, it should be used in well-ventilated areas to minimize exposure.

Related Pages