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Merck

A6664

4-Amidinophenylmethanesulfonyl fluoride hydrochloride

serine protease inhibitor

Synonym(s):

4-Amidinobenzylsulfonyl fluoride hydrochloride, p-APMSF

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About This Item

Empirical Formula (Hill Notation):
C8H9FN2O2S · HCl
CAS Number:
Molecular Weight:
252.69
UNSPSC Code:
12352202
NACRES:
NA.77
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
9083148
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assay

≥97% (silver nitrate titration)

form

powder

mp

190-191 ºC

solubility

H2O: 50 mM (Stable when aliquoted at −20°C. Half-life = 6 minutes in pH 7.0 buffer systems.)

storage temp.

−20°C

SMILES string

Cl[H].NC(=N)c1ccc(CS(F)(=O)=O)cc1

InChI

1S/C8H9FN2O2S.ClH/c9-14(12,13)5-6-1-3-7(4-2-6)8(10)11;/h1-4H,5H2,(H3,10,11);1H

InChI key

KHLLRHIUKOJXLL-UHFFFAOYSA-N

General description

4-Amidinophenylmethanesulfonyl fluoride hydrochloride is relatively nontoxic.

Application

4-Amidinophenylmethanesulfonyl fluoride hydrochloride has been used:
  • as a component of inhibitor cocktail for whole blood collection and separation of plasma
  • as a component of sodium dodecyl sulfate (SDS) sample buffer to prepare whole-cell extract
  • as a trypsin inhibitor to measure its inhibition efficiency and to determine the efficacy of the quantum dot fluorescence resonance energy transfer (FRET)-based enzymatic probes

Biochem/physiol Actions

4-Amidinophenylmethanesulfonyl fluoride hydrochloride (p-APMSF) can inhibit the trypsin-like proteinase produced by Fusarium culmorum. It is also capable of blocking bovine Factor Xa, human plasmin, and the human complement proteases, C1r and C1s.
Irreversible inhibitor of serine proteases with lysine or arginine substrate specificities. Effective concentration 10-100 μM.
Irreversible inhibitor of serine proteases with lysine or arginine substrate specificities. Effective concentration 10-100 μM. Frequently used to characterize newly discovered proteases.


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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