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Merck
CN

165304

D-(–)-2-氨基-5-膦酰戊酸

≥97% (HPLC), solid, NMDA receptor antagonist, Calbiochem®

别名:

D-(–)-2-氨基-5-膦酰戊酸, D-AP5,NMDA拮抗剂II,APV,D-APV,2-APV,D-2-氨基-5-磷酸戊酸

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关于此项目

经验公式(希尔记法):
C5H12NO5P
化学文摘社编号:
分子量:
197.13
UNSPSC Code:
12352106
NACRES:
NA.77
MDL number:
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产品名称

D-(–)-2-氨基-5-膦酰戊酸, Active enantiomer of DL-2-amino-5-phosphonopentanoic acid (AP5) that is a commonly used as a competitive NMDA receptor antagonist.

SMILES string

[P](=O)([O-])([O-])CCC[C@@H]([N+H3])C(=O)[O-]

InChI

1S/C5H12NO5P/c6-4(5(7)8)2-1-3-12(9,10)11/h4H,1-3,6H2,(H,7,8)(H2,9,10,11)/p-2/t4-/m1/s1

InChI key

VOROEQBFPPIACJ-SCSAIBSYSA-L

assay

≥97% (HPLC)

form

solid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze
desiccated (hygroscopic)
protect from light

color

white

solubility

dilute aqueous base: 1 mg/mL
water: 1 mg/mL

shipped in

ambient

storage temp.

2-8°C

Quality Level

Biochem/physiol Actions

主要靶标
NMDA受体拮抗剂
产物不与ATP竞争。
可逆:否
细胞渗透性:否

Disclaimer

毒性:刺激性(B)

General description

一种DL-2-氨基-5-膦基戊酸(AP5)的活性对映体,通常用作竞争性NMDA受体拮抗剂。还抑制辣椒素诱导的脊髓物质P的释放。

Other Notes

Malcangio, M., et al. 1998.Br. J. Pharmacol.125, 1625.
Schulte, M.K., et al. 1994.Brain Res. 649, 203.
Davis, S., et al. 1992.J. Neurosci. 12, 21.

Preparation Note

复溶后,等分并冷冻保存(-20°C)。储备液在-20°C条件下可稳定保存6个月。

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Jing Zhou et al.
eLife, 10 (2021-03-05)
Callosal projections from primary somatosensory cortex (S1) are key for processing somatosensory inputs and integrating sensory-motor information. How the callosal innervation pattern in S1 is formed during early postnatal development is not clear. We found that the normal termination pattern
Yu-Hong Zhang et al.
Cell stem cell, 28(8), 1483-1499 (2021-04-23)
The hypothalamus contains an astounding heterogeneity of neurons that regulate endocrine, autonomic, and behavioral functions. However, its molecular developmental trajectory and origin of neuronal diversity remain unclear. Here, we profile the transcriptome of 43,261 cells derived from Rax+ hypothalamic neuroepithelium
Hitomi Abe et al.
iScience, 25(3), 103927-103927 (2022-03-15)
Understanding the molecular mechanisms of gene regulation is pivotal for understanding how cells establish and modify their identities and functions. Multiple transcription factors (TFs) coordinate to alter gene expression in cells; however, a method to quantitatively analyze the activity of

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