4371-55-5 Usage
Uses
Used in Pharmaceutical Industry:
Phenylalanine, b-mercaptois used as a building block for the synthesis of proteins and enzymes, which are essential for various biological processes and functions. Its presence in the diet is crucial for maintaining overall health and proper bodily function.
Used in Food Industry:
Phenylalanine, b-mercaptois found in a variety of protein-rich foods, such as meat, fish, dairy products, soybeans, and lentils. It contributes to the nutritional value of these foods and supports the synthesis of essential proteins and enzymes in the body.
Used in Research and Development:
Phenylalanine, b-mercaptoserves as a valuable compound in scientific research and development, particularly in the study of protein synthesis, enzyme function, and the role of sulfur-containing amino acids in biological processes. It can also be used in the development of new pharmaceuticals and therapeutic agents targeting various health conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 4371-55-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,7 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4371-55:
(6*4)+(5*3)+(4*7)+(3*1)+(2*5)+(1*5)=85
85 % 10 = 5
So 4371-55-5 is a valid CAS Registry Number.
4371-55-5Relevant academic research and scientific papers
β-Substituted Cysteines as Sequestering Agents for Ethanol-Derived Acetaldehyde in Vivo
Nagasawa, Herbert T.,Elberling, James E.,Roberts, Jeanette C.
, p. 1373 - 1378 (2007/10/02)
A series of β-mono- and β,β-disubstituted cysteins were evaluated in rats as sequestering agents for metabolically generated acetaldehyde (AcH) during the oxidation of ethanol in vivo and compared against D-(-)-penicillamine.Both threo- (5) and erythro-β-
An Excursion into the Synthesis of Potential Angiotensin Converting Enzyme Inhibitors
Nitz, Theodore J.,Lindsey, John,Stammer, Charles H.
, p. 4029 - 4032 (2007/10/02)
An attempt to prepare dehydro analogues of 1 gave the expected tripeptide 2a, but rearrangement of a thiazolone derivative of ΔZ-Phe made only a thiazolinecarboxylic acid (8) available.The latter was also converted into a tripeptide (11) and both compounds, 2a and 11, showed moderate angiotensin converting enzyme inhibition.
