A fluorogenic substrate for DPP-4
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Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.

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GP-AMC (hydrobromide)

Item No. 34458

Technical Information
Formal Name
glycyl-N-(4-methyl-2-oxo-2H-1-benzopyran-7-yl)-L-prolinamide, monohydrobromide
CAS Number
115035-46-6
Synonyms
  • Gly-Pro-AMC
  • Gly-Pro-7-amido-4-methylcoumarin
Molecular Formula
C17H19N3O4 • HBr
Formula Weight
Purity
≥98%
Emission
440-460 nm
Excitation
340-360 nm
A solid
DMF: 10 mg/mlDMSO: 1 mg/mlPBS (pH 7.2): 10 mg/ml
λmax
328 nm
SMILES
CC(C1=CC=C(NC([C@H]2N(C(CN)=O)CCC2)=O)C=C1O3)=CC3=O.Br
InChi Code
InChI=1S/C17H19N3O4.BrH/c1-10-7-16(22)24-14-8-11(4-5-12(10)14)19-17(23)13-3-2-6-20(13)15(21)9-18;/h4-5,7-8,13H,2-3,6,9,18H2,1H3,(H,19,23);1H/t13-;/m0./s1
InChi Key
PASXTQMFJRHMLJ-ZOWNYOTGSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    GP-AMC is a fluorogenic substrate for dipeptidyl peptidase 4 (DPP-4).1,2 Upon enzymatic cleavage by DPP-4, 7-amino-4-methylcoumarin (AMC) is released and its fluorescence can be used to quantify DPP-4 activity. AMC displays excitation/emission maxima of 340-360/440-460 nm, respectively.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Matheeussen, V., Lambeir, A.-M., Jungraithmayr, W., et alMethod comparison of dipeptidyl peptidase IV activity assays and their application in biological samples containing reversible inhibitors. Clin. Chim. Acta 413(3-4), 456-462 (2012).

    2. Lammi, C., Bollati, C., Ferruzza, S., et alSoybean- and lupin-derived peptides inhibit DPP-IV activity on in situ human intestinal Caco-2 cells and ex vivo human serum. Nutrients 10(8), 1082 (2018).