D-AP5 (mM/ml), NMDA glutamate site antagonist (ab144482)
Key features and details
- NMDA glutamate site antagonist. 1 ml water soluble pack.
- CAS Number: 79055-68-8
- Purity: > 99%
- Soluble in 1 ml of water to give specified mM/ml concentration
- Form / State: Solid
- Source: Synthetic
製品の概要
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製品名
D-AP5 (mM/ml), NMDA glutamate site antagonist -
製品の詳細
NMDA glutamate site antagonist. 1 ml water soluble pack. -
別名
- APV
- D-APV
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生理活性の詳細
Competitive NMDA receptor glutamate site antagonist. More active form of DL-AP5.
Soluble in 1 ml water to give specified mM/ml concentration. Find out more. -
精製度
> 99% -
CAS 番号
79055-68-8 -
構造式
製品の特性
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体系名
D-(-)-2-Amino-5-phosphonopentanoic acid -
分子量
197.13 -
分子式
C5H12NO5P -
PubChem 登録番号
135342 -
保存方法
Store at +4°C. Store under desiccating conditions. The product can be stored for up to 12 months. -
溶解性
Soluble in 1 ml of water to give specified mM/ml concentration -
使用に関する注意
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
Refer to SDS for further information
Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
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SMILES 線形表記
N[C@H](CCCP(=O)(O)O)C(=O)O -
由来
Synthetic
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研究分野
画像
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2D chemical structure image of ab144482, D-AP5 (mM/ml), NMDA glutamate site antagonist
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Functional Studies - D-AP5 (mM/ml), NMDA glutamate site antagonist (ab144482)Case et al PLoS One. 2011;6(6):e20756. doi: 10.1371/journal.pone.0020756. Epub 2011 Jun 9. Fig 3. Reproduced under the Creative Commons license http://creativecommons.org/licenses/by/4.0/
Fractional current mediated by AMPARs increases between birth and hearing onset.
A: Representative mixed glutamatergic responses from P1, P5 and P9 neurons (average of 10 recordings), scaled to peak AMPA current; distinct AMPA and NMDA components visible in each trace. B: Same traces as in A, showing the mixed glutamatergic current, the pharmacologically isolated NMDAR component, and the response after application of AMPAR and NMDAR antagonists, D-APV and CNQX, which abolishes the glutamatergic response. All recordings in Mg++-free ACSF. Note change in scalebars for P9 recordings. C: Ratios of peak AMPA/NMDA current in 39 cells from slices P1-P12. During this period, AMPA/NMDA ratio increases as a function of age (p = 0.012, Kruskal-Wallis; P1/2 vs P9/10, p = 0.048; P7/8 vs P9/10, p = 0.30; P9/10 vs P11/12 p = 0.010; linear regression slope 0.14/day, r2 = 0.32; exponential fit r2 = 0.36). Filled black circles represent means ± SEMs at two-day intervals. Filled gray circles represent cells shown in A,B. D: Increase in AMPA/NMDA ratio with age is accompanied by small increases in average AMPA current (open circles, regressed to gray line) and decreases in average NMDAR current (filled circles, regressed to black line).
プロトコール
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
参考文献 (102)
ab144482 は 102 報の論文で使用されています。
- Fan S et al. Isoliquiritigenin modulates the activity of LTS and non-LTS cells in the ventrolateral preoptic area via GABAA receptors. Heliyon 9:e20620 (2023). PubMed: 37876454
- Li A et al. Disrupted population coding in the prefrontal cortex underlies pain aversion. Cell Rep 37:109978 (2021). PubMed: 34758316
- Rojas A et al. Activation of group I metabotropic glutamate receptors potentiates heteromeric kainate receptors. Mol Pharmacol 83:106-21 (2013). PubMed: 23066089
- Budisantoso T et al. Evaluation of glutamate concentration transient in the synaptic cleft of the rat calyx of Held. J Physiol 591:219-39 (2013). PubMed: 23070699
- Maroto M et al. Chondroitin sulfate, a major component of the perineuronal net, elicits inward currents, cell depolarization, and calcium transients by acting on AMPA and kainate receptors of hippocampal neurons. J Neurochem : (2013). PubMed: 23350646