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Sku CI32862_5_MG
Chem Impex
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Product Information

Product Name
Suc-Arg-Pro-Phe-His-Leu-Leu-Val-Tyr-AMC trifluoroacetate salt
Brand Name
Chem Impex
Product Number
32862
CAS
76524-84-0
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
133109983
IUPAC Name
4-5-(diaminomethylideneamino)-1-2-1-1-1-1-1-3-(4-hydroxyphenyl)-1-(4-methyl-2-oxochromen-7-yl)amino-1-oxopropan-2-ylamino-3-methyl-1-oxobutan-2-ylamino-4-methyl-1-oxopentan-2-ylamino-4-methyl-1-oxopentan-2-ylamino-3-(1H-imidazol-5-yl)-1-oxopropan-2-ylamino-1-oxo-3-phenylpropan-2-ylcarbamoylpyrrolidin-1-yl-1-oxopentan-2-ylamino-4-oxobutanoic acid
InChI Key
LRWWPXPMAGIGIX-UHFFFAOYSA-N
SMILES
CC1=CC(=O)OC2=C1C=CC(=C2)NC(=O)C(CC3=CC=C(C=C3)O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC4=CN=CN4)NC(=O)C(CC5=CC=CC=C5)NC(=O)C6CCCN6C(=O)C(CCCN=C(N)N)NC(=O)CCC(=O)O

Description

Suc-Arg-Pro-Phe-His-Leu-Leu-Val-Tyr-AMC trifluoroacetate salt is widely utilized in research focused on:

Biochemical Assays: This compound is often used in enzyme activity assays, particularly for proteases. Its structure allows for the specific cleavage by target enzymes, enabling researchers to measure enzyme kinetics effectively.

Drug Development: In pharmaceutical research, it serves as a model substrate for studying drug interactions with proteolytic enzymes, aiding in the design of more effective therapeutic agents.

Peptide Synthesis: The compound is valuable in peptide synthesis protocols, providing a stable and effective building block for creating complex peptide chains used in various applications.

Diagnostic Tools: It is utilized in the development of diagnostic kits for diseases where protease activity is a biomarker, allowing for early detection and monitoring of conditions.

Research on Protein-Protein Interactions: The compound can be employed in studies investigating protein interactions, helping scientists understand cellular processes and develop targeted therapies.