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About This Item
Empirical Formula (Hill Notation):
C15H14N2O2
CAS Number:
Molecular Weight:
254.28
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
244-809-9
MDL number:
Beilstein/REAXYS Number:
5066652
Product Name
L-Pyroglutamic acid 2-naphthylamide, ≥99% (TLC)
InChI key
BZEPQNMASTUAMY-ZDUSSCGKSA-N
InChI
1S/C15H14N2O2/c18-14-8-7-13(17-14)15(19)16-12-6-5-10-3-1-2-4-11(10)9-12/h1-6,9,13H,7-8H2,(H,16,19)(H,17,18)/t13-/m0/s1
SMILES string
O=C1CC[C@H](N1)C(=O)Nc2ccc3ccccc3c2
assay
≥99% (TLC)
form
powder
technique(s)
ligand binding assay: suitable
color
white to off-white
storage temp.
2-8°C
Quality Level
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Application
A substrate for pyroglutamate aminopeptidase. Used for differentiation of Group A streptococci and enterococci from other streptococci.
Biochem/physiol Actions
Pyroglutamic acid is known to participate in the gamma-glutamyl cycle. Recent studies show that a congenital metabolic error was associated with increased pyroglutamic excretion in urine.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
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C A Barboza et al.
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Studies on the Accumulation of L-Pyroglutamic Acid in Guinea Pig Epidermis
Sverre MarsteinM.D.
The Journal of Investigative Dermatology, 74(3), 135-138 (1980)
G A Hébert
Journal of clinical microbiology, 28(11), 2425-2431 (1990-11-01)
Reference strains and clinical isolates representing the newly defined species Staphylococcus lugdunensis and Staphylococcus schleiferi were examined with the battery of tests previously recommended (G.A. Hébert, C.G. Crowder, G.A. Hancock, W.R. Jarvis, and C. Thornsberry, J. Clin. Microbiol. 26:1939-1949, 1988)
Frida Martin et al.
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Parascaris univalens is a pathogenic parasite of foals and yearlings worldwide. In recent years, Parascaris spp. worms have developed resistance to several of the commonly used anthelmintics, though currently the mechanisms behind this development are unknown. The aim of this
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