Z-Gly-Pro-Arg-4MβNA acetate salt

Modify Date: 2024-01-02 14:58:47

Z-Gly-Pro-Arg-4MβNA acetate salt Structure
Z-Gly-Pro-Arg-4MβNA acetate salt structure
 Common Name Z-Gly-Pro-Arg-4MβNA acetate salt
CAS Number 66647-41-4 Molecular Weight 617.70
Density 1.4±0.1 g/cm3 Boiling Point N/A
Molecular Formula C32H39N7O6 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Z-Gly-Pro-Arg-4MβNA acetate salt


Z-Gly-Pro-Arg-4MβNA is the cleavage of the substrate of thrombin to release free 4-methoxy-2-naphthylamine (4MβNA). Free 4MβNA can be captured by 5-nitrosalicylaldehyde to produce an insoluble yellow fluorescent and marks the site of thrombin activity[1].

 Names

Name Z-Gly-Pro-Arg-4MβNA acetate salt
Synonym More Synonyms

 Z-Gly-Pro-Arg-4MβNA acetate salt Biological Activity

Description Z-Gly-Pro-Arg-4MβNA is the cleavage of the substrate of thrombin to release free 4-methoxy-2-naphthylamine (4MβNA). Free 4MβNA can be captured by 5-nitrosalicylaldehyde to produce an insoluble yellow fluorescent and marks the site of thrombin activity[1].
Related Catalog
References

[1]. Bushi D, et al. A novel histochemical method for the visualization of thrombin activity in the nervous system. Neuroscience. 2016 Apr 21;320:93-104.  

 Chemical & Physical Properties

Density 1.4±0.1 g/cm3
Molecular Formula C32H39N7O6
Molecular Weight 617.70
Exact Mass 617.296204
LogP 2.46
Index of Refraction 1.646

 Synonyms

Z-GLY-PRO-ARG-4MBNA COH
L-Argininamide, N-[(phenylmethoxy)carbonyl]glycyl-L-prolyl-N-(4-methoxy-2-naphthalenyl)-
N-[(Benzyloxy)carbonyl]glycyl-L-prolyl-N-(4-methoxy-2-naphthyl)-L-argininamide
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