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A8456

Sigma-Aldrich

Fluorure de 4-(2-aminoéthyl)-benzènesulfonyle hydrochloride

≥97.0% (HPLC)

Synonyme(s) :

AEBSF

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About This Item

Formule empirique (notation de Hill):
C8H10FNO2S · HCl
Numéro CAS:
Poids moléculaire :
239.69
Numéro Beilstein :
7604627
Numéro MDL:
Code UNSPSC :
12352202
ID de substance PubChem :
Nomenclature NACRES :
NA.77

Source biologique

synthetic (organic)

Niveau de qualité

Pureté

≥97.0% (HPLC)

Forme

powder

Pf

183-191  °C

Solubilité

H2O: 50 mg/mL (stable for up to six months if stored refrigerated at a pH of less than 7. If a pH of greater than 7 is required, pH adjustment should be made just prior to use.)

Température de stockage

−20°C

Chaîne SMILES 

FS(C1=CC=C(CCN)C=C1)(=O)=O.[H]Cl

InChI

1S/C8H10FNO2S.ClH/c9-13(11,12)8-3-1-7(2-4-8)5-6-10;/h1-4H,5-6,10H2;1H

Clé InChI

WRDABNWSWOHGMS-UHFFFAOYSA-N

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Application

4-(2-Aminoethyl)benzenesulfonyl fluoride hydrochloride (AEBSF) has been used:
  • as a protease inhibitor in plasma samples to prevent acylated ghrelin (AG) degradation
  • as a snake venom serine proteinase (SVSP) inhibitor in SVSP inhibition or AEBSF assay to test the involvement of SVSPs on the fibrinogen-clotting activity
  • as a component in NP-40 lysis buffer to resuspend cell pellets for preparing cell lysates

Les concentrations recommandées pour l′emploi sont comprises entre 0,1 et 1 mM.

Actions biochimiques/physiologiques

AEBSF can inhibit acetylcholinesterase (AChE).
Inhibiteur irréversible des protéases à sérine. Les constantes d′inhibition sont proches de celles du PMSF et du DFP. Il a été démontré que l′AEBSF inhibe la trypsine, la chymotrypsine, la plasmine, la kallikréine et la thrombine. Comme option de remplacement du PMSF ou du DFP, l′AEBSF offre une plus faible toxicité, une meilleure solubilité dans l′eau et une plus grande stabilité dans les solutions aqueuses. L′AEBSF a été utilisé en culture cellulaire à des concentrations allant jusqu′à 0,25 mM.

Pictogrammes

Corrosion

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Eye Dam. 1 - Skin Corr. 1A

Code de la classe de stockage

8A - Combustible, corrosive hazardous materials

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


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Consulter la Bibliothèque de documents

Ilario Mennella et al.
The Journal of nutrition, 145(9), 2169-2175 (2015-07-17)
Food palatability increases food intake and may lead to overeating. The mechanisms behind this observation are still largely unknown. The aims of this study were the following: 1) to elucidate the plasma responses of endocannabinoids, N-acylethanolamines, and gastrointestinal peptides to
Ignacio Pedrós et al.
Biochimica et biophysica acta, 1842(9), 1556-1566 (2014-06-03)
The present study had focused on the behavioral phenotype and gene expression profile of molecules related to insulin receptor signaling in the hippocampus of 3 and 6 month-old APPswe/PS1dE9 (APP/PS1) transgenic mouse model of Alzheimer's disease (AD). Elevated levels of
Sara Lind Jepsen et al.
The Journal of clinical endocrinology and metabolism, 105(1) (2019-10-15)
The gastrointestinal hormone ghrelin stimulates growth hormone secretion and appetite, but recent studies indicate that ghrelin also stimulates the secretion of the appetite-inhibiting and insulinotropic hormone glucagon-like peptide-1 (GLP-1). To investigate the putative effect of ghrelin on GLP-1 secretion in
Niina Aaltonen et al.
Biological procedures online, 22, 6-6 (2020-03-20)
Serine hydrolases (SHs) are a functionally diverse family of enzymes playing pivotal roles in health and disease and have emerged as important therapeutic targets in many clinical conditions. Activity-based protein profiling (ABPP) using fluorophosphonate (FP) probes has been a powerful
Robert J Snelgrove et al.
The Journal of allergy and clinical immunology, 134(3), 583-592 (2014-03-19)
The fungal allergen Alternaria alternata is implicated in severe asthma and rapid onset life-threatening exacerbations of disease. However, the mechanisms that underlie this severe pathogenicity remain unclear. We sought to investigate the mechanism whereby Alternaria was capable of initiating severe

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