194351-87-6 Usage
Description
L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-L-valyl-L-alanyl-L-leucyl-2-methylalanyl-L-valyl-L-alanyl-, methyl ester is a complex chemical compound composed of various amino acids linked in a specific sequence, with a methyl group attached to the carboxyl group of the terminal amino acid. L-Phenylalanine,
N-[(1,1-dimethylethoxy)carbonyl]-L-valyl-L-alanyl-L-leucyl-2-methylalanyl-L
-valyl-L-alanyl-, methyl ester is often utilized in research and pharmaceutical applications due to its potential biological and pharmacological properties, making it a valuable tool for studying protein structure and function, as well as for developing potential therapeutic agents.
Uses
Used in Pharmaceutical Research:
L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-L-valyl-L-alanyl-L-leucyl-2-methylalanyl-L-valyl-L-alanyl-, methyl ester is used as a research compound for exploring its potential biological activities and pharmacological effects. Its unique structure and properties make it a promising candidate for the development of new therapeutic agents.
Used in Protein Structure and Function Studies:
L-Phenylalanine,
N-[(1,1-dimethylethoxy)carbonyl]-L-valyl-L-alanyl-L-leucyl-2-methylalanyl-L
-valyl-L-alanyl-, methyl ester is employed in the study of protein structure and function, providing insights into the interactions between amino acids and their roles in protein folding, stability, and activity. Understanding these interactions can contribute to the advancement of protein engineering and the design of novel bioactive peptides.
Used in Drug Development:
L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-L-valyl-L-alanyl-L-leucyl-2-methylalanyl-L-valyl-L-alanyl-, methyl ester is used as a lead compound in drug development, with potential applications in the treatment of various diseases and conditions. Its unique sequence and properties may offer new avenues for the design of targeted therapeutic agents with improved efficacy and selectivity.
Used in Biochemical Assays and Diagnostics:
L-Phenylalanine,
N-[(1,1-dimethylethoxy)carbonyl]-L-valyl-L-alanyl-L-leucyl-2-methylalanyl-L
-valyl-L-alanyl-, methyl ester can be utilized in biochemical assays and diagnostic tools, serving as a substrate or inhibitor in the study of enzymatic activities and pathways related to amino acid metabolism and protein synthesis. Its application in these areas can contribute to the development of new diagnostic methods and therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 194351-87-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,3,5 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 194351-87:
(8*1)+(7*9)+(6*4)+(5*3)+(4*5)+(3*1)+(2*8)+(1*7)=156
156 % 10 = 6
So 194351-87-6 is a valid CAS Registry Number.