Pep2m
Pep2m is a peptide receptor inhibitor. Pep2m inhibits the interaction between the C-terminus of the AMPA-type glutamate receptor (GluA2) subunit and N-ethylmaleimide-sensitive fusion protein (NSF). Pep2m prevents synaptic long-term depression (LTD). Pep2m can reduce postsynaptic currents in neurons, AMPA-mediated currents in cultured hippocampal neurons, and AMPA receptor surface expression[1][2][3][4][5].
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- CAS 番号: 243843-42-7
- 分子式: C49H92N18O13S
- 分子量:1173.43
-
保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
iGluR アイソフォーム固有の製品をすべて表示
More
生物活性
製品説明
IC50 & Target
[1][2][3][4][5]|
AMPA Receptor |
体外実験
Pep2m reduces EPSC amplitude and blocks LTD in CA1 pyramidal cells of hippocampal slices by reducing the number of functional AMPARs[1].
Pep2m reduces the current response to locally applied AMPA in cultured hippocampal neurons[2].
Pep2m reduces the frequency of recorded AMPA-miniature excitatory postsynaptic currents (mEPSCs) in the presence of tetrodotoxin (TTX)[2].
Pep2m reduces the surface expression of AMPA receptors containing AMPA-type glutamate receptors (GluR2), but does not reduce the surface expression of NMDA receptors and the ingrowth aggregation of AMPA receptors[2].
Pep2m does not affect basal synaptic transmission and low-frequency stimulation (LFS)-induced LTD in young GluA2 KO mice, and does not affect basal synaptic transmission but restores LFS-induced LTD in mature GluA2 KO mice[3].
Pep2m reduces AMPA-induced radiolabeled norepinephrine ([3H]NA) but not AMPA-induced radiolabeled acetylcholine ([3H]Ach) release[5].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
体内実験
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Animal Model:Adult male C57B6J mice (8 weeks) [4]
-
Dosage:1 μL of 450 nM
-
Administration:ICV, once
-
Result:Impaired learning rate and long-term memory expression.
化学情報
-
CAS 番号 243843-42-7
-
分子量 1173.43
-
分子式 C49H92N18O13S
-
配列
Lys-Arg-Met-Lys-Val-Ala-Lys-Asn-Ala-Gln
-
シーケンスの短縮
KRMKVAKNAQ
-
輸送条件
Room temperature in continental US; may vary elsewhere.
-
保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
[1]. Lüthi A, et al.Hippocampal LTD expression involves a pool of AMPARs regulated by the NSF-GluR2 interaction. Neuron. 1999 Oct;24(2):389-99. [Content Brief]
[2]. Noel J, et al.Surface expression of AMPA receptors in hippocampal neurons is regulated by an NSF-dependent mechanism. Neuron. 1999 Jun;23(2):365-76. [Content Brief]
[3]. Cao F, et al. Hippocampal Long-Term Depression in the Presence of Calcium-Permeable AMPA Receptors. Front Synaptic Neurosci. 2018 Nov 13;10:41. [Content Brief]
[4]. Conboy L, et al. Stress at learning facilitates memory formation by regulating AMPA receptor trafficking through a glucocorticoid action. Neuropsychopharmacology. 2010 Feb;35(3):674-85. [Content Brief]
[5]. Pittaluga A, et al. Trafficking of presynaptic AMPA receptors mediating neurotransmitter release: neuronal selectivity and relationships with sensitivity to cyclothiazide. Neuropharmacology. 2006 Mar;50(3):286-96. [Content Brief]
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)