462-88-4 Usage
Description
3-UREIDOPROPIONIC ACID, also known as β-ureidopropionic acid, is an organic compound that serves as a vital metabolite in the synthesis of uracil and plays a crucial role in linking uracil to β-Alanine metabolism. It is an essential component in various biochemical processes and has potential applications in different industries.
Uses
Used in Pharmaceutical Industry:
3-UREIDOPROPIONIC ACID is used as an intermediate in the synthesis of various pharmaceutical compounds for its role in linking uracil to β-Alanine metabolism. This makes it a valuable component in the development of drugs targeting metabolic disorders and other related conditions.
Used in Biochemical Research:
3-UREIDOPROPIONIC ACID is used as a research tool in biochemical studies for its involvement in uracil and β-Alanine metabolism. It aids scientists in understanding the underlying mechanisms of these metabolic pathways and contributes to the advancement of knowledge in the field of biochemistry.
Used in Nutritional Supplements:
3-UREIDOPROPIONIC ACID is used as a nutritional supplement to support the synthesis of uracil and β-Alanine, which are essential for various physiological processes in the body. It can be incorporated into dietary supplements to promote overall health and well-being.
Check Digit Verification of cas no
The CAS Registry Mumber 462-88-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 462-88:
(5*4)+(4*6)+(3*2)+(2*8)+(1*8)=74
74 % 10 = 4
So 462-88-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H8N2O3/c5-4(9)6-2-1-3(7)8/h1-2H2,(H,7,8)(H3,5,6,9)/p-1
462-88-4Relevant articles and documents
-
Pojarlieff,I.G.
, p. 4307 - 4315 (1967)
-
New functional glycoluril derivatives
Chegaev,Kravchenko,Lebedev,Strelenko
, p. 32 - 33 (2007/10/03)
Functional glycoluril (2,4,6,8-tetraazabicyclo[3.3.0]octan-3,7-dione) derivatives containing 2-hydroxyethyl, carboxyl and amino groups were synthesised.
Mechanism of Asymmetric Production of D-Amino Acids from the Corresponding Hydantoins by Pseudomonas sp.
Yokozeki, Kenzo,Kubota, Koji
, p. 721 - 728 (2007/10/02)
The mechanism of asymmetric production of D-amino acids from the corresponding hydantoins by Pseudomonas sp.AJ-11220 was examined by investigating the properties of the enzymes involved in the hydrolysis of DL-5-substituted hydantoins.The enzymatic production of D-amino acids from the corresponding hydantoins by Pseudomonas sp.AJ-11220 involved the following two successive reactions; the D-isomer specific hydrolysis, i.e., the ring opening of D-5-substituted hydantoins to D-form N-carbamyl amino acids by an enzyme, D-hydantoin hydrolase (D-HYD hydrolase), followed by the D-isomer specific hydrolysis, i.e., the cleavage of N-carbamyl-D-amino acids to D-amino acids by an enzyme, N-carbamyl-D-amino acid hydrolase (D-NCA hydrolase).L-5-Substituted hydantoins not hydrolyzed by D-HYD hydrolase were converted to D-form 5-substituted hydantoins through spontaneous racemization under the enzymatic reaction conditions.It was proposed that almost all of the DL-5-substituted hydantoins were stoichiometrically and directly converted to the corresponding D-amino acids through the successive reactions of D-HYD hydrolase and D-NCA hydrolase in parallel with the spontaneous racemization of L-5-substituted hydantoins to those of DL-form.