AEBSF

AEBSF
Names
	IUPAC name 4-(2-Aminoethyl)benzenesulfonyl fluoride
	Other names Pefabloc SC
Identifiers
CAS Number	34284-75-8 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL1096339 ;
ChemSpider	1638 ;
DrugBank	DB07347 ;
MeSH	AEBSF
PubChem CID	1701;
CompTox Dashboard (EPA)	DTXSID40187844 ;
	InChI InChI=1S/C8H10FNO2S/c9-13(11,12)8-3-1-7(2-4-8)5-6-10/h1-4H,5-6,10H2 Key: MGSKVZWGBWPBTF-UHFFFAOYSA-N ; InChI=1/C8H10FNO2S/c9-13(11,12)8-3-1-7(2-4-8)5-6-10/h1-4H,5-6,10H2 Key: MGSKVZWGBWPBTF-UHFFFAOYAK;
	SMILES FS(=O)(=O)c1ccc(cc1)CCN;
Properties
Chemical formula	C8H10FNO2S.HCl
Molar mass	239.69 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

AEBSF or 4-(2-Aminoethyl) benzenesulfonyl fluoride hydrochloride is a water soluble, irreversible serine protease inhibitor with a molecular weight of 239.5 Da. It inhibits proteases like chymotrypsin, kallikrein, plasmin, thrombin, and trypsin. The specificity is similar to the inhibitor PMSF, nevertheless AEBSF is more stable at low pH values. Typical usage is 0.1 - 1.0 mM.

Mechanism of action

Both AEBSF and PMSF are sulfonyl fluorides and are sulfonylating agents.^[1] Sulfonyl fluorides act by reacting with the hydroxy group of the active site serine residue to form a sulfonyl enzyme derivative. This derivative may be stable for long periods of time except at high pH.^[2]

Use in cholesterol regulation studies

AEBSF is extensively used in studies aiming to describe cholesterol regulatory genes due to its potent ability to inhibit Site-1-protease (S1P). This serine protease, located in the Golgi apparatus, is responsible for activating the sterol regulatory element-binding proteins (SREBP). By selectively inhibiting S1P, AEBSF can be used to characterize the downstream result of SREBP inhibition and its influence on cholesterol regulation.

External links

The MEROPS online database for peptidases and their inhibitors: AEBSF
A Link to the ABRF group usegroup archive with an informative discussion of covalent modifications to proteins resulting from use of AEBSF: [1]

References

^ Powers JC, Asgian JL, Ekici OD, James KE. (2002). "Irreversible inhibitors of serine, cysteine, and threonine proteases". Chem. Rev. 102 (12): 4735–4736. PMID 12475205.{{cite journal}}: CS1 maint: multiple names: authors list (link)
^ Gold AM, Fahrney D. (1964). "SULFONYL FLUORIDES AS INHIBITORS OF ESTERASES. II. FORMATION AND REACTIONS OF PHENYLMETHANESULFONYL ALPHA-CHYMOTRYPSIN". Biochemistry. 1964 Jun;3:783-91. 3: 783–791. PMID 14211616.

[1] Powers JC, Asgian JL, Ekici OD, James KE. (2002). "Irreversible inhibitors of serine, cysteine, and threonine proteases". Chem. Rev. 102 (12): 4735–4736. PMID 12475205.{{cite journal}}: CS1 maint: multiple names: authors list (link)

[2] Gold AM, Fahrney D. (1964). "SULFONYL FLUORIDES AS INHIBITORS OF ESTERASES. II. FORMATION AND REACTIONS OF PHENYLMETHANESULFONYL ALPHA-CHYMOTRYPSIN". Biochemistry. 1964 Jun;3:783-91. 3: 783–791. PMID 14211616.

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