Interesting facts
Interesting Facts about 2-(Methylamino)butanedioic Acid
2-(Methylamino)butanedioic acid, often referred to in scientific contexts for its various roles in biochemical pathways, is a fascinating compound that showcases the intersection of organic chemistry and biochemistry. Here are some intriguing points about this compound:
- Biological Significance: This compound plays a crucial role as an intermediate in amino acid metabolism. As a derivative of aspartic acid, it participates in the synthesis of proteins, which are essential for cellular structure and function.
- Potential Therapeutic Use: Research has suggested that derivatives of 2-(methylamino)butanedioic acid might exhibit neuroprotective and metabolic benefits, hinting at its potential applications in treating various health conditions.
- Presence in Nature: Several non-essential amino acids, to which 2-(methylamino)butanedioic acid is closely related, are naturally synthesized within organisms, underlining the compound's importance in sustaining life processes.
- Structural Unique Characteristics: The presence of a methylamino group contributes to its chemical reactivity, allowing it to form various derivatives that may have distinct biological properties.
- Chemical Interactions: This compound can interact with different biological molecules, influencing enzyme activities and metabolic pathways, which makes it an interesting subject for further study in metabolic engineering.
In summary, 2-(methylamino)butanedioic acid is not only a product of basic metabolic processes but also a promising candidate for therapeutic applications. Its structural features and reactivity offer a rich area for scientific exploration, and its significance in biochemistry continues to unravel exciting possibilities for future research.
Synonyms
N-Methyl-DL-aspartic acid
17833-53-3
2-(methylamino)butanedioic acid
2-(Methylamino)succinic acid
N-methylaspartic acid
EU52DFC4WJ
N-Methyl-l-aspartic acid HCl
CHEMBL275325
DTXSID20859971
N-Me-Asp-OH
n-methyl-dl-aspartate
DL-Aspartic acid, N-methyl-
N-Me-DL-Asp-OH
UNII-EU52DFC4WJ
DL-2-METHYLAMINOSUCCINIC ACID
MFCD00065918
H-D-MeAsp-OH
Aspartic acid,N-methyl-
N-METHYL-L-ASPARTIC ACID HYDROCHLORIDE
SCHEMBL167682
DL-N-METHYLASPARTIC ACID
DTXCID30209721
CHEBI:181378
METHYL ASPARTIC ACID, DL-
HMS3266A05
HMS3370L14
HMS3411A03
HMS3652P20
HMS3675A03
BCP21209
NSC16206
BDBM50002343
STK246904
(R,S)-2-(Methylamino)succinic acid
AKOS005066589
CS-W018216
FM16185
HY-W017500
NMA;(+)-2-(Methylamino)succinic acid
NCGC00015666-02
NCGC00015666-03
NCGC00015666-04
NCGC00095062-01
NCGC00095062-02
AC-24120
BP-12733
DS-14547
SY035118
DB-044327
DB-054563
2-(Methylamino)succinic acid (Me-DL-Asp-OH)
G73908
AB01326367-02
EN300-6958635
BRD-A02508087-001-01-1
BRD-A02508087-001-02-9
Q27277365
964-924-4
Solubility of 2-(Methylamino)butanedioic Acid (C5H9NO4)
2-(Methylamino)butanedioic acid, commonly known as a derivative of aspartic acid, possesses notable solubility characteristics:
These factors play a crucial role in its use in chemical reactions and biological systems. Understanding the solubility can help in tailoring effective formulations and enhancing bioavailability in pharmaceutical applications.