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About This Item
Linear Formula:
C11H13N3O5
CAS Number:
Molecular Weight:
285.25
NACRES:
NA.83
PubChem Substance ID:
UNSPSC Code:
12352204
EC Number:
230-748-5
MDL number:
Beilstein/REAXYS Number:
2818758
Product Name
L-Glutamic acid γ-(4-nitroanilide), γ-glutamyl transpeptidase substrate
Quality Level
assay
≥98% (HPLC)
form
powder
solubility
formic acid: 50 mg/mL, clear to slightly hazy
storage temp.
2-8°C
SMILES string
N[C@@H](CCC(=O)Nc1ccc(cc1)[N+]([O-])=O)C(O)=O
InChI
1S/C11H13N3O5/c12-9(11(16)17)5-6-10(15)13-7-1-3-8(4-2-7)14(18)19/h1-4,9H,5-6,12H2,(H,13,15)(H,16,17)/t9-/m0/s1
InChI key
WMZTYIRRBCGARG-VIFPVBQESA-N
General description
Substrate for γ-glutamyl transpeptidase
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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L Dvoráková et al.
General physiology and biophysics, 15(5), 403-413 (1996-10-01)
The initial rate kinetics of rat kidney gamma-glutamyl transpeptidase were measured using L-gamma-glutamyl-p-nitroanilide and glycyl-glycine as the donor and the acceptor substrate, respectively. Experimental data were fitted with the initial rate equation, and the obtained results indicated that: (1) Michaelis
Gololobov MYu et al.
The Biochemical journal, 304 ( Pt 3), 869-876 (1994-12-15)
Acyl-transfer catalysed by gamma-glutamyltranspeptidase from bovine kidney was studied using gamma-L- and gamma-D-Glu-p-nitroanilide as the donor and GlyGly as the acceptor. The transfer of the gamma-Glu group to GlyGly was shown to be accompanied by transfer of the gamma-Glu group
P M Verhoeff et al.
Clinica chimica acta; international journal of clinical chemistry, 175(2), 129-134 (1988-07-15)
In this paper we compare the measurement of catalytic activity concentrations of gamma-glutamyltransferase with the non-carboxylated and the carboxylated substrate in preparations of different origin. Fresh human sera, commercial test sera and preparations of gamma-glutamyltransferase purified from human liver, porcine