L-Threonine-15N - 80681-09-0

L-Threonine-15N

Catalog Number: EVT-467006
CAS Number: 80681-09-0
Molecular Formula: C4H9NO3
Molecular Weight: 120.11 g/mol
The product is for non-human research only. Not for therapeutic or veterinary use.
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Product Introduction

Description
L-Threonine-15N is a stable isotope-labeled amino acid that is commonly used in scientific research. It is a non-essential amino acid that is synthesized in the body and is involved in various biological processes.
Applications in Various Fields
L-Threonine-15N has various applications in scientific research, including its role in drug development and clinical trials. It has been used to study the metabolism of amino acids and to investigate the effects of amino acid supplementation on muscle protein synthesis. L-Threonine-15N has also been used in environmental research to study the effects of nitrogen pollution on ecosystems and to develop sustainable agriculture practices. In industrial research, L-Threonine-15N has been used in manufacturing processes to improve product quality and efficiency, with health and safety considerations being taken into account.

Properties

CAS Number

80681-09-0

Product Name

L-Threonine-15N

IUPAC Name

(2S,3R)-2-(15N)azanyl-3-hydroxybutanoic acid

Molecular Formula

C4H9NO3

Molecular Weight

120.11 g/mol

InChI

InChI=1S/C4H9NO3/c1-2(6)3(5)4(7)8/h2-3,6H,5H2,1H3,(H,7,8)/t2-,3+/m1/s1/i5+1

InChI Key

AYFVYJQAPQTCCC-SZEKAKMSSA-N

SMILES

CC(C(C(=O)O)N)O

Canonical SMILES

CC(C(C(=O)O)N)O

Isomeric SMILES

C[C@H]([C@@H](C(=O)O)[15NH2])O
Method of Synthesis or Extraction
L-Threonine-15N can be synthesized using various methods, including chemical synthesis, enzymatic synthesis, and fermentation. Chemical synthesis involves the reaction of 15N-labeled ammonia with 2-ketobutyric acid, which is then converted to L-Threonine-15N. Enzymatic synthesis involves the use of enzymes to catalyze the reaction between 15N-labeled ammonia and 2-ketobutyric acid. Fermentation involves the use of microorganisms to produce L-Threonine-15N. The efficiency and yield of each method vary, with fermentation being the most efficient and yielding the highest amount of L-Threonine-15N. Environmental and safety considerations should also be taken into account when choosing a method of synthesis or extraction.
Chemical Structure and Biological Activity
L-Threonine-15N has the same chemical structure as L-Threonine, with the addition of a stable isotope of nitrogen. It is involved in various biological processes, including protein synthesis, immune function, and wound healing. L-Threonine-15N is also a precursor to glycine and serine, which are important neurotransmitters. Its mechanism of action and biological targets are not fully understood, but it is believed to act as a substrate for various enzymes and to play a role in signal transduction.
Biological Effects
L-Threonine-15N has been shown to have various biological effects on cell function and signal transduction. It has been found to enhance protein synthesis and immune function, as well as to promote wound healing. L-Threonine-15N has also been shown to have potential therapeutic effects, including the treatment of liver disease, inflammatory bowel disease, and cancer. However, it may also have toxic effects at high doses, including liver damage and neurological disorders.
Future Perspectives and Challenges
The use and study of L-Threonine-15N are currently limited by its high cost and limited availability. Possible solutions and improvements include the development of more efficient methods of synthesis or extraction and the use of alternative stable isotopes. Future trends and prospects in the application of L-Threonine-15N in scientific research include its potential use in personalized nutrition and the development of new therapies for various diseases.
Conclusion
L-Threonine-15N is a stable isotope-labeled amino acid that has various applications in scientific research. Its method of synthesis or extraction, chemical structure, biological activity, biological effects, applications, future perspectives, and challenges have been discussed in this paper. Further research is needed to fully understand the mechanism of action and biological targets of L-Threonine-15N and to develop more efficient and cost-effective methods of synthesis or extraction.

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