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SUC-LEU-LEU-VAL-TYR-AMC

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SUC-LEU-LEU-VAL-TYR-AMC Basic information

Product Name:
SUC-LEU-LEU-VAL-TYR-AMC
Synonyms:
  • Z-LLVY-AMC
  • succinyl-leucyl-leucyl-valyl-tyrosyl-methylcoumarinamide
  • SUC-LLVY-AMC
  • SUC-LEU-LEU-VAL-TYR-AMC
  • SUC-LEU-LEU-VAL-TYR-MCA
  • SUC-LEU-LEU-VAL-TYR-7-AMINO-4-METHYLCOUMARIN
  • SUCCINYL-L-LEUCYL-L-LEUCYL-L-VALYL-L-TYROSINE-4-METHYLCOUMARINYL-7-AMIDE
  • SUCCINYL-L-LEUCYL-L-LEUCYL-L-VALYL-L-TYROSINE 4-METHYLCOUMARYL-7-AMIDE
CAS:
94367-21-2
MF:
C40H53N5O10
MW:
763.88
Product Categories:
  • Pepetides
Mol File:
94367-21-2.mol
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SUC-LEU-LEU-VAL-TYR-AMC Chemical Properties

Boiling point:
1116.8±65.0 °C(Predicted)
Density 
1.249±0.06 g/cm3(Predicted)
storage temp. 
-20°C
solubility 
Soluble in DMSO (up to 20 mg/ml), or in DMF (up to 10 mg/ml)
pka
4.69±0.10(Predicted)
form 
Lyophilized solid
color 
White to Off-White
Sequence
Suc-Leu-Leu-Val-Tyr-AMC
Stability:
Stable for 1 year from date of purchase as supplied. Solutions in DMSO or DMF may be stored at -20°C for up to 1 month.
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Safety Information

WGK Germany 
3

MSDS

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SUC-LEU-LEU-VAL-TYR-AMC Usage And Synthesis

Description

Suc-Leu-Leu-Val-Tyr-AMC (94367-21-2) is a fluorogenic substrate for the chymotryptic activity of the 20S proteasome1 and other chymotrypsin-like proteases, as well as calpains2. A commonly used substrate for assaying proteasomal enzymatic activity.3,4 Excitation max.: 360 nm; emission max.: 460 nm.

Uses

Suc-Leu-Leu-Val-Tyr-AMC is a fluorgenic substrate for chymotrypsin-like proteases, as well as calpains. It can be used to treat tuberculosis.

Definition

ChEBI: A tetrapeptide compound with a succinyl group at the N-terminal and a 7-amino-4-methylcoumarin group at the C-terminal.

Biochem/physiol Actions

In the presence of chymotrypsin-like enzyme activity, the fluorophore, 7-amido-4-methylcoumarin is released from N-succinyl-Leu-Leu-Val-Tyr-7-amido-4-methylcoumarin. The fluorescence obtained is a measure of the enzyme activity.6

References

1) Stein et al. (1996), Kinetic characterization of the chymotryptic activity of the 20S proteasome; Biochemistry, 35 3899 2) Sasaki et al. (1984), Comparative specificity and kinetic studies on porcine calpain I and calpain II with naturally occurring peptides and synthetic fluorogenic substrates; J. Biol. Chem., 259 12489 3) Hamouda et al. (2014), The small heat shock protein B8 (HSPB8) confers resistance to bortezomib by promoting autophagic removal of misfolded proteins in multiple myeloma cells; Oncotarget, 5 6252 4) Min et al. (2017), USP14 inhibitor attenuates cerebral ischemia/reperfusion-induced neuronal injury in mice; J. Neurochem,, 140 826

SUC-LEU-LEU-VAL-TYR-AMCSupplier

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