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Merck

A5930

N-Acetyl-Asp-Glu

≥97% (TLC), mGluR3 agonist, powder or crystals

Synonym(e):

N-Acetylaspartylglutamicacid, NAAG, Spaglumic acid

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€ 340,85

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Über diesen Artikel

Empirische Formel (Hill-System):
C11H16N2O8
CAS-Nummer:
Molekulargewicht:
304.25
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.32
MDL number:
Assay:
≥97% (TLC)
Form:
powder or crystals
Quality level:
Storage condition:
(Tightly closed. Dry)

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Produktname

N-Acetyl-Asp-Glu, ≥97% (TLC)

SMILES string

CC(=O)NC(CC(O)=O)C(=O)NC(CCC(O)=O)C(O)=O

InChI key

OPVPGKGADVGKTG-UHFFFAOYSA-N

InChI

1S/C11H16N2O8/c1-5(14)12-7(4-9(17)18)10(19)13-6(11(20)21)2-3-8(15)16/h6-7H,2-4H2,1H3,(H,12,14)(H,13,19)(H,15,16)(H,17,18)(H,20,21)

assay

≥97% (TLC)

form

powder or crystals

optical activity

[α]22/D −34.5°, c = 1.1 in H2O(lit.)

storage condition

(Tightly closed. Dry)

color

white to off-white

solubility

H2O: 50 mg/mL

storage temp.

−20°C

Quality Level

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Dieser Artikel
A2559773077A6339
assay

≥97% (TLC)

assay

≥97% (HPLC)

assay

97%

assay

~99% (HPLC)

form

powder or crystals

form

powder

form

powder or crystals

form

powder

Quality Level

200

Quality Level

100

Quality Level

100

Quality Level

200

storage temp.

−20°C

storage temp.

−20°C

storage temp.

2-8°C

storage temp.

−20°C

storage condition

(Tightly closed. Dry)

storage condition

-

storage condition

-

storage condition

-

solubility

H2O: 50 mg/mL

solubility

-

solubility

-

solubility

H2O: 1 mg/mL

General description

Research area: Neuroscience

Application

N-Acetyl-Asp-Glu has been used in N-acetylated α-linked acidic dipeptidase (NAALADase) assay and affinity experiments.[1][2]. It has also been used as a metabolite standard in liquid chromatography-mass spectrometry (LC-MS) targeted metabolomics analysis[3] and mass-spectroscopy-based stable isotope-resolved metabolomics (SIRM) with 13C515N2-labeled-glutamine.[4]

Biochem/physiol Actions

Endogenous neurotransmitter localized to neurons with high affinity for metabotropic glutamate receptors, mGluR3. It is an antagonist at NMDA receptors. Catabolized by carboxypeptidase II, which is expressed on astrocyte membranes, to N-acetylaspartate and glutamate.
Endogenous neurotransmitter localized to neurons with high affinity for metabotropic glutamate receptors, mGluR3; NMDA receptor antagonist.
N-Acetyl-Asp-Glu (NAAG) is an abundant neuropeptide and neurotransmitter found in the mammalian brain.[5] NAAG acts as an agonist for metabotropic glutamate receptors, mGluR3.[3] In addition, it also acts as an antagonist for the N-methyl d-aspartate (NMDA) receptors.[5] It yields N-acetyl aspartate and glutamate through glutamate carboxypeptidase II (GCP II) dependent pathway. Thus, it serves as a key glutamate reservoir in cancer cells. NAAG levels in plasma could be used as a non-invasive biomarker for tumor progression.[3]

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Disclaimer

Store desiccated.

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pictograms

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signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Lagerklasse

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Die Dokumentenbibliothek aufrufen

Multi-omics approaches to disease
Yehudit H, et al.
Genome Biology (2017)
Frank Jessen et al.
Schizophrenia bulletin, 39(1), 197-205 (2011-09-15)
BACKGROUND : Imbalance of glutamatergic neurotransmission has been proposed as a key mechanism underlying symptoms of schizophrenia. The neuropetide N-acetylaspartylglutamate (NAAG) modulates glutamate release. NAAG provides a component of the proton magnetic resonance spectrum (1H-MRS) in humans. The signal of NAAG
Rosane Gomez et al.
Biological psychiatry, 71(3), 239-246 (2011-08-23)
Ethanol modulates glutamate and γ-aminobutyric (GABA) function. However, little is known about the acute pharmacologic effects of ethanol on levels of GABA, glutamate, and other metabolites measurable in the human cortex in vivo with proton magnetic resonance spectroscopy ((1)H-MRS). Eleven
Preparation and affinity identification of glutamic acid-urea small molecule analogs in prostate cancer
Zhang Z, et al.
Oncology Letters, 12(2), 1001-1006 (2016)
Hyeong Hun Lee et al.
Magnetic resonance in medicine, 82(1), 33-48 (2019-03-13)
To develop a robust method for brain metabolite quantification in proton magnetic resonance spectroscopy (1 H-MRS) using a convolutional neural network (CNN) that maps in vivo brain spectra that are typically degraded by low SNR, line broadening, and spectral baseline

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