64298-91-5 Usage
Description
2-AMINO-2-METHYL-4-PENTENOIC ACID, also known as AMPA, is a non-proteinogenic amino acid that is structurally similar to glutamate. It belongs to the class of amino acids and has been identified in certain marine organisms. AMPA functions as a potent agonist of the AMPA receptor, a subtype of ionotropic glutamate receptors. It is used as a research tool to study the pharmacology and physiology of the central nervous system, particularly in relation to excitatory neurotransmission. Furthermore, it has been studied for its potential therapeutic benefits in the treatment of various neurological and psychiatric disorders.
Uses
Used in Pharmaceutical Industry:
2-AMINO-2-METHYL-4-PENTENOIC ACID is used as a research tool for studying the pharmacology and physiology of the central nervous system. It aids in understanding excitatory neurotransmission and the role of AMPA receptors in various neurological and psychiatric disorders.
Used in Research Applications:
2-AMINO-2-METHYL-4-PENTENOIC ACID is used as a potent agonist of the AMPA receptor to investigate the mechanisms of ionotropic glutamate receptor function and its implications in neurological and psychiatric disorders.
Used in Drug Development:
2-AMINO-2-METHYL-4-PENTENOIC ACID is studied for its potential therapeutic benefits in the treatment of various neurological and psychiatric disorders, making it a candidate for drug development and therapeutic intervention.
Check Digit Verification of cas no
The CAS Registry Mumber 64298-91-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,2,9 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 64298-91:
(7*6)+(6*4)+(5*2)+(4*9)+(3*8)+(2*9)+(1*1)=155
155 % 10 = 5
So 64298-91-5 is a valid CAS Registry Number.
64298-91-5Relevant articles and documents
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Aidene,Barbot,Miginiac
, p. 117 - 127 (2007/10/03)
A new general synthesis of C-subtituted α-aminoacids is described, using at first the regioselective reaction between α-unsaturated organozincs and N-(phenylsulfanyl)iminoesters.
