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S9761

Sigma-Aldrich

N-Succinyl-Ala-Ala-Pro-Phe-7-amido-4-methylcoumarin

leucine aminopeptidase substrate, ≥98% (HPLC), powder

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About This Item

Formule empirique (notation de Hill):
C34H39N5O9
Numéro CAS:
88467-45-2
Poids moléculaire :
661.70
Numéro MDL:
MFCD00080246
Code UNSPSC :
12352204
ID de substance PubChem :
24899855
Nomenclature NACRES :
NA.32

product name

N-Succinyl-Ala-Ala-Pro-Phe-7-amido-4-methylcoumarin, Leucine aminopeptidase substrate

Pureté

≥98% (HPLC)

Forme

powder

Solubilité

methanol: 50 mg/mL, clear, colorless

Température de stockage

−20°C

Chaîne SMILES 

CC(NC(=O)CCC(O)=O)C(=O)NC(C)C(=O)N1CCCC1C(=O)NC(Cc2ccccc2)C(=O)Nc3ccc4C(C)=CC(=O)Oc4c3

InChI

1S/C34H39N5O9/c1-19-16-30(43)48-27-18-23(11-12-24(19)27)37-32(45)25(17-22-8-5-4-6-9-22)38-33(46)26-10-7-15-39(26)34(47)21(3)36-31(44)20(2)35-28(40)13-14-29(41)42/h4-6,8-9,11-12,16,18,20-21,25-26H,7,10,13-15,17H2,1-3H3,(H,35,40)(H,36,44)(H,37,45)(H,38,46)(H,41,42)

Clé InChI

FMVUZZZUYBXQGR-UHFFFAOYSA-N

Conditionnement

Bottomless glass bottle. Contents are inside inserted fused cone.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

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G B Irvine et al.
Analytical biochemistry, 185(2), 304-307 (1990-03-01)
A simple, inexpensive, and sensitive assay for peptidase activity has been devised. The assay was performed in a microtiter plate and was based on fluorogenic peptide substrates, many of which are commercially available. 7-Amino-4-methyl coumarin the fluorescent product liberated during
Julián Gamboa-Delgado et al.
Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology, 158(4), 251-258 (2010-12-21)
The effect of diet on larval growth, anionic trypsinogen gene expression (ssetryp1), and trypsin (EC 3.4.21.4) and chymotrypsin (EC 3.4.21.1) activities was assessed in Solea senegalensis. Changes in larval carbon stable isotope (δ(13)C) composition were used to estimate carbon assimilation.
I Sohár et al.
Acta biologica Hungarica, 42(1-3), 265-274 (1991-01-01)
Previously, MMP-7ases were isolated from rat skeletal muscle by gel filtration and anion exchange chromatography. The enzyme that hydrolyzed succinyl-Ala-Ala-Pro-Phe-AMC (AMC: 7-amino-4-methyl-coumarin) was inhibited by EDTA. In this study we attempted to isolate MMP-7ase from mouse kidney. The isolation procedure
Activity of cathepsin H,B and metalloproteinase in the serum of patients with acute myocardial infarction.
A László et al.
Clinica chimica acta; international journal of clinical chemistry, 210(3), 233-235 (1992-09-30)
H Sawada et al.
Experientia, 39(4), 377-378 (1983-04-15)
The action of a chymotrypsin-like enzyme from sperm extract from the ascidian Halocynthia roretzi was studied using several substrates. It was found that the most susceptible substrate had the most powerful inhibitory effect on fertilization in this animal. Among the
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