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Z-Asp-Glu-Val-Asp-7-Amino-4-trifluoromethylcoumarin_Molecular_structure_CAS_)
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Z-Asp-Glu-Val-Asp-7-Amino-4-trifluoromethylcoumarin

Catalog No. 03AFC138Z Name MP Biomedicals
CAS Number Website http://www.mpbio.com
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SYNONYMS

IUPAC name
(4S)-4-[(2S)-2-{[(benzyloxy)carbonyl]amino}-3-carboxypropanamido]-4-{[(1S)-1-{[(1S)-2-carboxy-1-{[2-oxo-4-(trifluoromethyl)-2H-chromen-7-yl]carbamoyl}ethyl]carbamoyl}-2-methylpropyl]carbamoyl}butanoic acid
IUPAC Traditional name
(4S)-4-[(2S)-2-{[(benzyloxy)carbonyl]amino}-3-carboxypropanamido]-4-{[(1S)-1-{[(1S)-2-carboxy-1-{[2-oxo-4-(trifluoromethyl)chromen-7-yl]carbamoyl}ethyl]carbamoyl}-2-methylpropyl]carbamoyl}butanoic acid
Synonyms
Z-Asp-Glu-Val-Asp-AFC
Z-DEVD-AFC

DATABASE IDS

PROPERTIES

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DETAILS

Description (English)
A fluorogenic substrate for Caspase-3 (CPP32, YAMA). Also acts as a substrate for granzyme B-processed ICE-LAP3. Reaction can be monitored by a blue to green shift in fluorescence upon cleavage of the AFC fluorophore. Also a substrate for caspase-6, caspase-7, caspase-8, and caspase-10.
Excitation max.: ~400 nm, Emission max.: ~505 nm

REFERENCES

  • Keramaris, E., et al. 2000. Mol. Cell Neurosci. 15, 368.
  • Thornberry, N.A., and Lazebnik, Y. 1998. Science 281, 1312.
  • Kluck, R.M., et al. 1997. Science 275, 1132.
  • Talanian, J., et al. 1997. J. Biol. Chem. 272, 9677.
  • Chinnaiyan, A.M., et al. 1996. Curr. Biol. 6, 897.
  • Nicholson, D.W., et al. 1995. Nature 376, 37.