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Merck

P1999

Sigma-Aldrich

PEAQX 四钠 水合物

≥98% (HPLC)

别名:

NVP-AAM077 四钠 水合物, [ [[(1S)-1-(4-溴苯基)乙基] 氨基](1,2,3,4-四氢-2,3-二氧代-5-喹喔啉基)甲基] 膦酸 四钠 水合物

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About This Item

经验公式(希尔记法):
C17H13BrN3Na4O5P · xH2O
分子量:
542.14 (anhydrous basis)
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.77

品質等級

化驗

≥98% (HPLC)

形狀

powder

儲存條件

desiccated

顏色

white to beige

溶解度

water: 10 mg/mL

儲存溫度

−20°C

SMILES 字串

[Na+].[Na+].[Na+].[Na+].[H]O[H].C[C@H](NC(c1cccc2nc([O-])c([O-])nc12)P([O-])([O-])=O)c3ccc(Br)cc3

InChI

1S/C17H17BrN3O5P.4Na.H2O/c1-9(10-5-7-11(18)8-6-10)19-17(27(24,25)26)12-3-2-4-13-14(12)21-16(23)15(22)20-13;;;;;/h2-9,17,19H,1H3,(H,20,22)(H,21,23)(H2,24,25,26);;;;;1H2/q;4*+1;/p-4/t9-,17?;;;;;/m0...../s1

InChI 密鑰

SMGAGBKXHAHCGQ-VSYRWHDMSA-J

應用

PEAQX四钠水合物已被用作大鼠 和小鼠的N-甲基-D-天冬氨酸 (NMDA) 受体 2A (NR2A) 拮抗剂。

生化/生理作用

PEAQX对N-甲基-D-天冬氨酸 (NMDA) 受体2A (NR2A) 的特异性高于对N-甲基-D-天冬氨酸 (NMDA) 受体 2B (NR2B) 的特异性, 并诱导纹状体细胞凋亡。它在激活caspase-3方面的效力不如其立体异构体NVP-AAM007。
NMDA 受体拮抗剂。

特點和優勢

该化合物是受体分类及信号转导手册上谷氨酸受体(离子通道家族)页面上的特色化合物。想要浏览手册的其他页面, 请单击此处
这种化合物是神经科学研究的特色产品。点击此处发现更多特色神经科学产品。在sigma.com/discover-bsm可了解更多关于生物活性小分子的其他研究领域。

象形圖

Exclamation mark

訊號詞

Warning

危險分類

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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Adolescents display high levels of interactions with peers relative to other age groups, with these interactions further enhanced by ethanol under some circumstances. Understanding of the neural mechanisms underlying these high levels of social interactions is important given that alcohol
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Psychopharmacology, 231(8), 1797-1807 (2013-09-18)
NMDA antagonists consistently produce social inhibition in adult animals, although effects of these manipulations on social behavior of adolescents are relatively unknown. The aim of this study was to assess potential age differences in the socially inhibitory effects of the
N C Anastasio et al.
Neuroscience, 163(4), 1181-1191 (2009-08-06)
The mechanism underlying phencyclidine (PCP)-induced apoptosis in perinatal rats and the development of schizophrenia-like behaviors is incompletely understood. We used antagonists for N-methyl-D-aspartate (NMDA) receptor subunit NR2A- and NR2B-containing NMDA receptor to test the hypothesis that the behavioral and apoptotic
Yves P Auberson et al.
Bioorganic & medicinal chemistry letters, 12(7), 1099-1102 (2002-03-23)
NMDA antagonists derived from 5-phosphonomethyl-1,4-dihydroquinoxaline-2,3-dione (3a) are potent anticonvulsant agents, and display strong protective effects in the electroshock-induced convulsion assay in mice. Their preference for the human NMDAR 1A/2A over 1A/2B subunit composition was optimized, leading to (1RS,1'S)-PEAQX (9r), which
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British journal of pharmacology, 141(3), 508-516 (2004-01-14)
(2S*,3R*)-1-(biphenyl-4-carbonyl)piperazine-2,3-dicarboxylic acid (PBPD) is a moderate affinity, competitive N-methyl-d-aspartate (NMDA) receptor antagonist with an atypical pattern of selectivity among NMDA receptor 2 subunit (NR2) subunits. We now describe the activity of several derivatives of PBPD tested at both rat brain

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