A3401

Ala-Ala-Phe-7-amido-4-methylcoumarin

protease substrate

• Synonyme(s) : H-Ala-Ala-Phe-AMC
• Formule empirique (notation de Hill) : C₂₅H₂₈N₄O₅
• Numéro CAS: 62037-41-6
• Poids moléculaire : 464.51
• NACRES: NA.32
• PubChem Substance ID: 24890766
• UNSPSC Code: 12352204
• MDL number: MFCD00070149

Propriétés

• Quality Segment: 200
• assay: ≥98% (TLC)
• form: powder
• solubility: ethanol: 20 mg/mL, clear, colorless to light yellow
• storage temp.: 2-8°C
• SMILES string: CC(N)C(=O)NC(C)C(=O)NC(Cc1ccccc1)C(=O)Nc2ccc3C(C)=CC(=O)Oc3c2
• InChI: 1S/C25H28N4O5/c1-14-11-22(30)34-21-13-18(9-10-19(14)21)28-25(33)20(12-17-7-5-4-6-8-17)29-24(32)16(3)27-23(31)15(2)26/h4-11,13,15-16,20H,12,26H2,1-3H3,(H,27,31)(H,28,33)(H,29,32)
• InChI key: FVRLYIFIDKXFHU-UHFFFAOYSA-N

Description

General description

Substrate for chymotrypsin and tripeptidyl peptidaseII.

Ala-Ala-Phe-7-amido-4-methylcoumarin is a fluorogenic substrate for the proteolytic activity. It is a positively charged substrate molecule.

Application

Ala-Ala-Phe-7-amido-4-methylcoumarin has been used:

• in the preparation of the reaction mixture for enzymatic assays
• to initiate the enzyme reaction in tripeptidyl peptidase-1 (TPP1) enzyme activity assay
• to initiate the assay reaction in lysosomal hydrolases activity assay

Informations sur la sécurité

• Classe de stockage: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)