123642-57-9 Usage
Uses
Used in Neurotransmission Research:
L-GLUTAMIC ACID, ALPHA-(DMNB-CAGED), HCL is used as a research tool for studying the role of glutamic acid in neurotransmission and its effects on biological systems. Its unique caged property enables precise control over the release of glutamic acid, facilitating the investigation of its interactions with other neurotransmitters and receptors.
Used in Metabolic Studies:
L-GLUTAMIC ACID, ALPHA-(DMNB-CAGED), HCL is utilized as a research compound in metabolic studies, particularly in understanding the role of glutamic acid in various metabolic pathways. The controlled release of the compound allows for the examination of its impact on cellular metabolism and energy production.
Used in Pharmaceutical Development:
L-GLUTAMIC ACID, ALPHA-(DMNB-CAGED), HCL is employed as a potential therapeutic agent in the development of drugs targeting neurological disorders. Its ability to modulate neurotransmission upon activation can be harnessed to develop treatments for conditions such as epilepsy, Parkinson's disease, and Alzheimer's disease.
Used in Drug Delivery Systems:
L-GLUTAMIC ACID, ALPHA-(DMNB-CAGED), HCL is used as a component in drug delivery systems, particularly for targeted drug release in specific areas of the body. The caged property allows for the compound to be activated only upon reaching the desired location, ensuring precise drug delivery and minimizing side effects.
Used in Biochemical Assays:
L-GLUTAMIC ACID, ALPHA-(DMNB-CAGED), HCL is utilized as a reagent in biochemical assays to measure the activity of enzymes involved in glutamic acid metabolism. The controlled release of the compound enables the accurate assessment of enzyme activity and the study of metabolic pathways.
Used in Educational Purposes:
L-GLUTAMIC ACID, ALPHA-(DMNB-CAGED), HCL is employed as an educational tool in teaching and learning about neurotransmitters, their functions, and the techniques used to study them. L-GLUTAMIC ACID, ALPHA-(DMNB-CAGED), HCL's unique properties provide a hands-on approach to understanding the principles of neurotransmission and the importance of glutamic acid in the nervous system.
Check Digit Verification of cas no
The CAS Registry Mumber 123642-57-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,6,4 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 123642-57:
(8*1)+(7*2)+(6*3)+(5*6)+(4*4)+(3*2)+(2*5)+(1*7)=109
109 % 10 = 9
So 123642-57-9 is a valid CAS Registry Number.
123642-57-9Relevant academic research and scientific papers
Synthesis of Photolabile "Precursors" of Amino Acid Neurotransmitters
Wilcox, Mary,Viola, Randall W.,Johnson, Katherine W.,Billington, Andrew P.,Carpenter, Barry K.,et al.
, p. 1585 - 1589 (2007/10/02)
The synthesis of photolabile precursors of the neurotransmitters for the aspartic acid, glutamic acid, glycine, and γ-aminobutyric acid receptors are reported.These compounds are designed for the rapid, photochemically initiated release of the neurotransmitter.The importance of rapidly photolyzed, inert (toward a neuronal receptor) precursors of neurotransmitters is in chemical kinetic investigations of the reactions involving the neuronal receptors.In the past, such studies have been hampered because of the insufficient time resolution of the available techniques.A photolyzable precursor of carbamoylcholine, an amino-group-containing analogue of acetylcholine, has been used previously to make measurements of currents flowing through the acetylcholine receptor channel within 100 μs.
