Aminooxy-PEG7-methane - 1370698-27-3
Aminooxy-PEG7-methane
Catalog Number: BT-259382
CAS Number: 1370698-27-3
Molecular Formula: C15H33NO8
Molecular Weight: 355.43
The product is for non-human research only. Not for therapeutic or veterinary use.
Product Introduction
Description
Aminooxy-PEG7-methane is a chemical compound that has gained significant attention in scientific research due to its potential therapeutic and industrial applications. It is a derivative of aminooxy compounds, which are known for their ability to react with carbonyl groups in proteins and other biomolecules. Aminooxy-PEG7-methane is a water-soluble compound that has a molecular weight of 287.36 g/mol.
Properties
CAS Number
1370698-27-3
Product Name
Aminooxy-PEG7-methane
IUPAC Name
O-[2-[2-[2-[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethyl]hydroxylamine
Molecular Formula
C15H33NO8
Molecular Weight
355.43
InChI
InChI=1S/C15H33NO8/c1-17-2-3-18-4-5-19-6-7-20-8-9-21-10-11-22-12-13-23-14-15-24-16/h2-16H2,1H3
InChI Key
DGGSCAFEGLNJGW-UHFFFAOYSA-N
SMILES
COCCOCCOCCOCCOCCOCCOCCON
Solubility
Soluble in DMSO
Synonyms
Aminooxy-PEG7-methane
Method of Synthesis or Extraction
Aminooxy-PEG7-methane can be synthesized using various methods, including the reaction of aminooxyacetic acid with PEG7-methane sulfonyl chloride. This method involves the use of organic solvents and requires careful handling due to the potential hazards associated with the use of sulfonyl chlorides. Another method involves the reaction of aminooxyacetic acid with PEG7-methane to form a stable amide bond. This method is more environmentally friendly and yields a higher purity product. However, it requires longer reaction times and higher temperatures.
Chemical Structure and Biological Activity
Aminooxy-PEG7-methane has a unique chemical structure that consists of a PEG7-methane backbone with an aminooxy group attached to it. The aminooxy group is responsible for the compound's ability to react with carbonyl groups in proteins and other biomolecules. This reaction can lead to the formation of stable adducts that can be used for various applications, including drug development and protein labeling.
Aminooxy-PEG7-methane has been shown to have potent biological activity, particularly in the inhibition of enzymes that are involved in various cellular processes. For example, it has been shown to inhibit the activity of glyceraldehyde-3-phosphate dehydrogenase (GAPDH), an enzyme that plays a critical role in glycolysis. Inhibition of GAPDH can lead to the accumulation of toxic metabolites and cell death. Aminooxy-PEG7-methane has also been shown to inhibit the activity of other enzymes, including aldose reductase and acetylcholinesterase.
Biological Effects
The biological effects of aminooxy-PEG7-methane are diverse and depend on the specific target and cellular context. Inhibition of GAPDH by aminooxy-PEG7-methane has been shown to induce apoptosis in cancer cells, making it a potential therapeutic agent for cancer treatment. Aminooxy-PEG7-methane has also been shown to inhibit the activity of acetylcholinesterase, an enzyme that is involved in the breakdown of the neurotransmitter acetylcholine. Inhibition of acetylcholinesterase can lead to increased levels of acetylcholine in the brain, which can improve cognitive function and memory.
Applications
Aminooxy-PEG7-methane has potential applications in various fields, including medical research, environmental research, and industrial research. In medical research, aminooxy-PEG7-methane can be used as a tool for drug development and protein labeling. It can also be used as a potential therapeutic agent for cancer treatment and neurodegenerative diseases.
In environmental research, aminooxy-PEG7-methane can be used to study the effects of carbonyl stress on ecosystems. It can also be used in pollution management to monitor the levels of carbonyl compounds in the environment.
In industrial research, aminooxy-PEG7-methane can be used in manufacturing processes to improve product quality and efficiency. It can also be used in the development of new materials and coatings.
Future Perspectives and Challenges
Despite the potential applications of aminooxy-PEG7-methane, there are still limitations in its use and study. One of the main challenges is the lack of understanding of its mechanism of action and specificity towards different targets. Another challenge is the potential toxicity of aminooxy-PEG7-methane, which needs to be carefully evaluated before its use in therapeutic applications.
To overcome these challenges, future research should focus on elucidating the mechanism of action of aminooxy-PEG7-methane and identifying its specific targets. This will enable the development of more specific and potent inhibitors. Future research should also focus on evaluating the safety and toxicity of aminooxy-PEG7-methane in different cellular contexts and animal models.
In conclusion, aminooxy-PEG7-methane is a promising compound with potential applications in various fields. Its unique chemical structure and potent biological activity make it a valuable tool for drug development, protein labeling, and environmental research. However, further research is needed to fully understand its mechanism of action and potential toxicity.
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