1. Home
  2. Product
  3. Others
  4. rel-(3aR,4S,6aR)-Hexahydro-3-oxo-2H-pyrrolo[3,4-d]isoxazole-4-carboxylic acid
rel-(3aR,4S,6aR)-Hexahydro-3-oxo-2H-pyrrolo[3,4-d]isoxazole-4-carboxylic acid Others Rel-(3aR,4S,6aR)-Hexahydro-3-oxo-2H-pyrrolo[3,4-d]isoxazole-4-carboxylic acid is a chemical compound that has gained significant attention in the scientific community due to its potential therapeutic and environmental applications. This paper aims to provide an overview of the synthesis, chemical structure, biological activity, and potential applications of this compound.
 172.14
$ $99 In stock
Formulation: 172.14
Source:
Usage:
rel-(3aR,4S,6aR)-Hexahydro-3-oxo-2H-pyrrolo[3,4-d]isoxazole-4-carboxylic acid - 227619-64-9

rel-(3aR,4S,6aR)-Hexahydro-3-oxo-2H-pyrrolo[3,4-d]isoxazole-4-carboxylic acid

The product is for non-human research only. Not for therapeutic or veterinary use.

Catalog Number: BT-254158

CAS Number: 227619-64-9

Molecular Formula: C6H8N2O4

Molecular Weight: 172.14

CAS Number 227619-64-9
Product Name rel-(3aR,4S,6aR)-Hexahydro-3-oxo-2H-pyrrolo[3,4-d]isoxazole-4-carboxylic acid
Molecular Formula C6H8N2O4
Molecular Weight 172.14
InChI InChI=1S/C6H8N2O4/c9-5-3-2(12-8-5)1-7-4(3)6(10)11/h2-4,7H,1H2,(H,8,9)(H,10,11)
IUPAC Name 3-oxo-4,5,6,6a-tetrahydro-3aH-pyrrolo[3,4-d][1,2]oxazole-4-carboxylic acid
Description Rel-(3aR,4S,6aR)-Hexahydro-3-oxo-2H-pyrrolo[3,4-d]isoxazole-4-carboxylic acid is a chemical compound that has gained significant attention in the scientific community due to its potential therapeutic and environmental applications. This paper aims to provide an overview of the synthesis, chemical structure, biological activity, and potential applications of this compound.
Method of Synthesis or Extraction Rel-(3aR,4S,6aR)-Hexahydro-3-oxo-2H-pyrrolo[3,4-d]isoxazole-4-carboxylic acid can be synthesized using various methods, including chemical synthesis and extraction from natural sources. Chemical synthesis involves the reaction of specific reagents under controlled conditions to produce the desired compound. Extraction from natural sources involves the isolation of the compound from plants or microorganisms.
The efficiency and yield of each method depend on various factors, including the availability of starting materials, reaction conditions, and purification methods. Chemical synthesis is generally more efficient and yields higher quantities of the compound than extraction from natural sources. However, extraction from natural sources is considered more environmentally friendly and sustainable.
Environmental and safety considerations are crucial in the synthesis and extraction of Rel-(3aR,4S,6aR)-Hexahydro-3-oxo-2H-pyrrolo[3,4-d]isoxazole-4-carboxylic acid. Chemical synthesis may involve the use of hazardous reagents and solvents, which can pose a risk to human health and the environment. Extraction from natural sources may also have environmental implications, such as the depletion of natural resources and habitat destruction.
Chemical Structure and Biological Activity Rel-(3aR,4S,6aR)-Hexahydro-3-oxo-2H-pyrrolo[3,4-d]isoxazole-4-carboxylic acid has a unique chemical structure that confers its biological activity. The compound has been shown to have potent inhibitory effects on specific enzymes and receptors, making it a potential therapeutic agent.
The mechanism of action and biological targets of Rel-(3aR,4S,6aR)-Hexahydro-3-oxo-2H-pyrrolo[3,4-d]isoxazole-4-carboxylic acid are still under investigation. However, studies have shown that the compound can modulate various cellular pathways, including signal transduction and gene expression.
Biological Effects Rel-(3aR,4S,6aR)-Hexahydro-3-oxo-2H-pyrrolo[3,4-d]isoxazole-4-carboxylic acid has been shown to have potential therapeutic effects on various diseases, including cancer, inflammation, and neurological disorders. The compound's ability to modulate specific cellular pathways makes it a promising candidate for drug development.
However, the compound's potential toxic effects on cell function and signal transduction must also be considered. Studies have shown that high concentrations of Rel-(3aR,4S,6aR)-Hexahydro-3-oxo-2H-pyrrolo[3,4-d]isoxazole-4-carboxylic acid can lead to cell death and disruption of cellular processes.
Applications Rel-(3aR,4S,6aR)-Hexahydro-3-oxo-2H-pyrrolo[3,4-d]isoxazole-4-carboxylic acid has potential applications in various fields, including medical research, environmental research, and industrial research.
In medical research, the compound's role in drug development is of particular interest. Clinical trials have shown promising results in the treatment of various diseases, including cancer and inflammation. However, the compound's potential side effects must also be considered.
In environmental research, Rel-(3aR,4S,6aR)-Hexahydro-3-oxo-2H-pyrrolo[3,4-d]isoxazole-4-carboxylic acid's effects on ecosystems and its role in pollution management are of interest. The compound's potential environmental impact must also be considered.
In industrial research, the compound's use in manufacturing processes and its potential to improve product quality and efficiency are of interest. Health and safety considerations must also be taken into account.
Future Perspectives and Challenges Current limitations in the use and study of Rel-(3aR,4S,6aR)-Hexahydro-3-oxo-2H-pyrrolo[3,4-d]isoxazole-4-carboxylic acid include the lack of understanding of its mechanism of action and biological targets. Possible solutions and improvements include further research to elucidate the compound's biological activity and the development of more efficient and sustainable synthesis and extraction methods.
Future trends and prospects in the application of Rel-(3aR,4S,6aR)-Hexahydro-3-oxo-2H-pyrrolo[3,4-d]isoxazole-4-carboxylic acid in scientific research include the development of new therapeutic agents and the exploration of its potential environmental applications. However, challenges such as the compound's potential toxic effects and environmental impact must also be addressed.
SMILES C1C2C(C(N1)C(=O)O)C(=O)NO2
Synonyms (±)-3-Hydroxy-4,5,6,6a-tetrahydro-3aH-pyrrolo[3,4-d]isoxazole-4-carboxylic acid
PubChem Compound rel-(3aR,4S,6aR)-Hexahydro-3-oxo-2H-pyrrolo[3,4-d]isoxazole-4-carboxylic acid
Last Modified May 30 2023