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G0141

Sigma-Aldrich

L-Glutamic acid γ-(4-methoxy-β-naphthylamide)

≥98% (TLC), powder

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About This Item

Empirical Formula (Hill Notation):
C16H18N2O4
CAS Number:
24723-50-0
Molecular Weight:
302.33
MDL number:
MFCD00037728
UNSPSC Code:
12352204
PubChem Substance ID:
24895008
NACRES:
NA.83

product name

L-Glutamic acid γ-(4-methoxy-β-naphthylamide),

Assay

≥98% (TLC)

Quality Level

200

form

powder

solubility

1 N HCl: ethanol, 1:1: 25 mg/mL, clear, colorless to faintly yellow

storage temp.

−20°C

SMILES string

OC([C@@H](N)CCC(NC1=CC2=CC=CC=C2C(OC)=C1)=O)=O

InChI

1S/C16H18N2O4/c1-22-14-9-11(8-10-4-2-3-5-12(10)14)18-15(19)7-6-13(17)16(20)21/h2-5,8-9,13H,6-7,17H2,1H3,(H,18,19)(H,20,21)

InChI key

DUNDTSUHZJULAX-UHFFFAOYSA-N

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Application

L-Glutamic acid γ-(4-methoxy-β-naphthylamide) has been used in histochemical staining of HepG2 cells for γ-glutamyl transpeptidase (GGT) subcellular localization.

Biochem/physiol Actions

L-Glutamic acid γ-(4-methoxy-β-naphthylamide) or GMNA is a synthetic substrate of γ-glutamyl transpeptidase (GGT).

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Pictograms

Health hazard
GHS08

Signal Word

Warning

Hazard Statements

H351

Precautionary Statements

P281

Hazard Classifications

Carc. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Matthew B West et al.
Archives of biochemistry and biophysics, 504(2), 177-181 (2010-09-14)
The cell surface enzyme γ-glutamyl transpeptidase (GGT) is expressed by human hepatocellular carcinomas (HCCs). HCCs arise from malignant transformation of hepatocytes and are the most common form of primary liver cancer. Identification of tumor-specific, post-translational modifications of GGT may provide
Aflatoxin B~ 1 and 2-acetylaminofluorene induced hepatic carcinogenicity and gamma-glutamyltranspeptidase expression via chronic feeding in rats
Liao JW, et al.
The American Journal of Medicine, 44(1) , 37-50 (2002)
Fatima Dahboul et al.
PloS one, 7(9), e43190-e43190 (2012-09-18)
S-nitrosoglutathione (GSNO) involved in storage and transport of nitric oxide ((•)NO) plays an important role in vascular homeostasis. Breakdown of GSNO can be catalyzed by γ-glutamyltransferase (GGT). We investigated whether vascular GGT influences the vasorelaxant effect of GSNO in isolated
Carlos David López-Torres et al.
The journal of gene medicine, 24(8), e3439-e3439 (2022-07-12)
Hepatocellular carcinoma (HCC) is one of the deadliest cancers worldwide, often preceded by cirrhosis and usually diagnosed at advanced stages; therefore, identifying molecular changes at early stages is an attractive strategy for detection and timely treatment. Here, we investigated the

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