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Merck

P5891

L-Pyroglutamic acid 2-naphthylamide

≥99% (TLC), suitable for ligand binding assays

Synonyme(s) :

L-Pyroglutamic acid β-naphthylamide, L-Pyrrolidonyl-β-naphthylamide, N1-(2-Naphthyl)-L-pyroglutamic acid, PYR

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A propos de cet article

Formule empirique (notation de Hill) :
C15H14N2O2
Numéro CAS:
Poids moléculaire :
254.28
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
244-809-9
MDL number:
Beilstein/REAXYS Number:
5066652
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Nom du produit

L-Pyroglutamic acid 2-naphthylamide, ≥99% (TLC)

Quality Level

assay

≥99% (TLC)

form

powder

technique(s)

ligand binding assay: suitable

color

white to off-white

storage temp.

2-8°C

SMILES string

O=C1CC[C@H](N1)C(=O)Nc2ccc3ccccc3c2

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

InChI key

BZEPQNMASTUAMY-ZDUSSCGKSA-N

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.


pictograms

Environment

signalword

Warning

hcodes

pcodes

Hazard Classifications

Aquatic Acute 1

Classe de stockage

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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Jean-Sébastien Jouhanneau et al.
Nature communications, 9(1), 1540-1540 (2018-04-20)
A defining feature of cortical layer 2/3 excitatory neurons is their sparse activity, often firing in singlets of action potentials. Local inhibitory neurons are thought to play a major role in regulating sparseness, but which cell types are recruited by
S Santisi et al.
Journal of applied microbiology, 127(3), 618-629 (2019-03-09)
The aims of this study were: (i) the characterization of the structure of the indigenous microbial community associated with the sediments under study; (ii) the isolation and characterization of microbial consortia able to degrade the aged hydrocarbons contaminating the sediments
Alaa Alachkar et al.
Frontiers in pharmacology, 8, 709-709 (2017-10-28)
The involvement of histamine H3 receptors (H3Rs) in memory is well known, and the potential of H3R antagonists in therapeutic management of neuropsychiatric diseases, e.g., Alzheimer disease (AD) is well established. Therefore, the effects of histamine H3 receptor (H3R) antagonist