SUC-LEU-LEU-VAL-TYR-AMC
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
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.
MSDS
- Language:English Provider:SigmaAldrich
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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