CAS 94367-21-2|Suc-Leu-Leu-Val-Tyr-AMC

Introduction:Basic information about CAS 94367-21-2|Suc-Leu-Leu-Val-Tyr-AMC, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameSuc-Leu-Leu-Val-Tyr-AMC
CAS Number94367-21-2Molecular Weight763.87600
Density1.249g/cm3Boiling Point1116.8ºC at 760mmHg
Molecular FormulaC40H53N5O10Melting Point/
MSDSUSAFlash Point629.2ºC

Names

Namesuccinyl-Leu-Leu-Val-Tyr-7-amino-4-methylcoumarin
SynonymMore Synonyms

Suc-Leu-Leu-Val-Tyr-AMC BiologicalActivity

DescriptionSuc-Leu-Leu-Val-Tyr-AMC is a fluorogenic substrate. Sequence: Suc-Leu-Leu-Val-Tyr.
Related CatalogSignaling Pathways >>Others >>OthersDye ReagentsPeptidesResearch Areas >>Others
In VitroSuc-Leu-Leu-Val-Tyr-AMC (Suc-LLVY) is a membrane-permeable calpain-specific fluorogenic substrate, pteolytic hydrolysis of the peptidyl-7-amino bond liberates the highly fluorescent 7-amino-4-methylcoumarin (AMC) moiety[1]. The effectof TGF-β on hydrolysis of these substrates (e.g Suc-Leu-Leu-Val-Tyr-AMC) are assessed. Biliary epithelial H69 cells are incubated with 10, 1, 0.1, or 0 ng/mL TGF-β for 24 h. Substrate hydrolysis is then fluorometrically assessed in cytosolic extracts. Basal activity is 1.12, 8.33, and 14.52 nmol AMC/mg protein/min for suc-LLVY-AMC, z-LLE-AMC, and z-LLL-AMC hydrolysis, respectively[2].
Kinase AssayImmunoprecipitation is carried out for the two sets of samples, using the same amount of protein. The 20 S and 26 S proteasome immunoprecipitates are washed with 50 mM Hepes/KOH (pH 7.5), and 50 mM Hepes/KOH (pH 7.5) containing 2 mMATP, respectively, prior to the determination of peptidase activity using 50 μM suc-Leu- Leu-Val-Tyr-AMC as substrate in these buffers[3].
References

[1]. Roberta L. Debiasi, et al. Reovirus-Induced Apoptosis Is Preceded by Increased Cellular Calpain Activity and Is Blocked by Calpain Inhibitors. J Virol. 1999 Jan; 73(1): 695–701.

[2]. Tadlock L, et al. Transforming growth factor-beta inhibition of proteasomal activity: a potential mechanism of growth arrest. Am J Physiol Cell Physiol. 2003 Aug;285(2):C277-85. Epub 2003 Mar 19.

[3]. Gardner RC, et al. Characterization of peptidyl boronic acid inhibitors of mammalian 20 S and 26 S proteasomes and their inhibition of proteasomes in cultured cells. Biochem J. 2000 Mar, 2:447-54.

Chemical & Physical Properties

Density1.249g/cm3
Boiling Point1116.8ºC at 760mmHg
Molecular FormulaC40H53N5O10
Molecular Weight763.87600
Flash Point629.2ºC
Exact Mass763.37900
PSA233.24000
LogP5.17700
Index of Refraction1.577
InChIKeyUVFAEQZFLBGVRM-MSMWPWNWSA-N
SMILESCc1cc(=O)oc2cc(NC(=O)C(Cc3ccc(O)cc3)NC(=O)C(NC(=O)C(CC(C)C)NC(=O)C(CC(C)C)NC(=O)CCC(=O)O)C(C)C)ccc12
Storage condition−20°C

Safety Information

Personal Protective EquipmentEyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADRNONH for all modes of transport
WGK Germany3

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Synonyms

z-llvy-amc
suc-leu-leu-val-tyr-amc
suc-llvy-amc
suc-leu-leu-val-tyr-7-amino-4-methylcoumarin
chymotrypsin substrate iii,fluorogenic
n-succinyl-leu-leu-val-tyr 7-amido-4-methylcoumarin
MFCD00080248
suc-leu-leu-val-tyr-mca
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