184901-82-4

AAF-CMK TFA Chemical Structure
184901-82-4

Chemical Structure

AAF-CMK TFA

Synonym(s): Ala-ala-phe-chloromethylketone tfa; N-Ala-Ala-Phe-CMK; Tripeptidyl Peptidase inhibitor II

  • CAS No.: 184901-82-4
  • Formula:C18H23ClF3N3O5
  • Molecular Weight:453.84

IUPAC Name: (S)-2-amino-N-((S)-1-amino-1-oxopropan-2-yl)-N-((S)-4-chloro-3-oxo-1-phenylbutan-2-yl)propanamide 2,2,2-trifluoroacetate

InChIKey: MFLWHUDUNKUYEQ-SQRKDXEHSA-N

SMILES: C[C@@H](C(N)=O)N(C([C@H](C)N)=O)[C@@H](CC1=CC=CC=C1)C(CCl)=O.O=C(O)C(F)(F)F

Biological Activity: AAF-CMK TFA (Ala-ala-phe-chloromethylketone tfa; N-Ala-Ala-Phe-CMK) is a subtilisin-type serine peptidase that removes tripeptides from the free NH2 termini of oligopeptides. AAF-CMK TFA is an irreversible inhibitor of TPPII and is typically used at concentrations of 10-100 μM. It does not significantly interfere with the chymotrypsin-like activity of the proteasome. AAF-CMK also inhibits bleomycin hydrolase and puromycin-sensitive aminopeptidase when used at a concentration of 50 μM.

Cat. No. Product Name Purity Description Pricing
HY-129407
AAF-CMK TFA AAF-CMK TFA (Ala-ala-phe-chloromethylketone tfa; N-Ala-Ala-Phe-CMK) is a subtilisin-type serine peptidase that removes tripeptides from the free NH2 termini of oligopeptides. AAF-CMK TFA is an irreversible inhibitor of TPPII and is typically used at concentrations of 10-100 μM. It does not significantly interfere with the chymotrypsin-like activity of the proteasome. AAF-CMK also inhibits bleomycin hydrolase and puromycin-sensitive aminopeptidase when used at a concentration of 50 μM.
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This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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