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(R)-3-Hydroxy-2-ureido-butyric acid, a naturally occurring metabolite derived from the amino acid threonine, plays a crucial role in the conversion of homocysteine to methionine. This process is vital for maintaining balanced levels of methionine and homocysteine in the human body. (R)-3-Hydroxy-2-ureido-butyric acid features a 3-hydroxy-2-ureido-butyric acid moiety and an R-configuration, which contribute to its potential applications in medicine and biochemistry. Ongoing research aims to elucidate its role in the human body and explore its therapeutic potential.

879552-80-4

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879552-80-4 Usage

Uses

Used in Pharmaceutical Industry:
(R)-3-Hydroxy-2-ureido-butyric acid is used as a potential therapeutic agent for neurological disorders due to its involvement in the conversion of homocysteine to methionine, which may have implications for brain health and function.
Used in Diagnostics:
(R)-3-Hydroxy-2-ureido-butyric acid is used as a possible biomarker for certain health conditions, given its role in the conversion of homocysteine to methionine, which can be indicative of various health issues when imbalanced.
Used in Biochemical Research:
(R)-3-Hydroxy-2-ureido-butyric acid serves as a subject of interest in biochemical research to better understand its role in the human body and its potential applications in medicine and biochemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 879552-80-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,9,5,5 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 879552-80:
(8*8)+(7*7)+(6*9)+(5*5)+(4*5)+(3*2)+(2*8)+(1*0)=234
234 % 10 = 4
So 879552-80-4 is a valid CAS Registry Number.

879552-80-4Downstream Products

879552-80-4Relevant academic research and scientific papers

New hydantoinases from thermophilic microorganisms - Synthesis of enantiomerically pure D-amino acids

Keil,Schneider,Rasor

, p. 1257 - 1260 (2007/10/02)

A series of 14 D-α-amino acids were prepared in high chemical and optical yields from the corresponding racemic hydantoins by employing two novel hydantoinases from thermophilic microorganisms.

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