3-(Pyrazol-1-yl)-L-alanine - 2734-48-7
3-(Pyrazol-1-yl)-L-alanine
Catalog Number: BT-3559480
CAS Number: 2734-48-7
Molecular Formula: C6H9N3O2
Molecular Weight: 155.15 g/mol
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Product Introduction
Description
3-(Pyrazol-1-yl)-L-alanine is a chemical compound that has gained significant attention in scientific research due to its potential biological activity and diverse applications. This paper aims to provide an overview of the synthesis methods, chemical structure, biological activity, and various applications of 3-(Pyrazol-1-yl)-L-alanine.
Properties
CAS Number
2734-48-7
Product Name
3-(Pyrazol-1-yl)-L-alanine
IUPAC Name
(2S)-2-amino-3-pyrazol-1-ylpropanoic acid
Molecular Formula
C6H9N3O2
Molecular Weight
155.15 g/mol
InChI
InChI=1S/C6H9N3O2/c7-5(6(10)11)4-9-3-1-2-8-9/h1-3,5H,4,7H2,(H,10,11)/t5-/m0/s1
InChI Key
PIGOPELHGLPKLL-UHFFFAOYSA-N
SMILES
C1=CN(N=C1)CC(C(=O)O)N
Canonical SMILES
C1=CN(N=C1)CC(C(=O)O)N
Method of Synthesis or Extraction
Several methods have been developed for the synthesis of 3-(Pyrazol-1-yl)-L-alanine. One commonly used method involves the reaction of pyrazole with L-alanine in the presence of a suitable catalyst. This method offers good efficiency and yield, with minimal environmental and safety considerations. Another approach involves the condensation of pyrazole with L-alanine using a coupling agent such as N,N'-dicyclohexylcarbodiimide (DCC) or N,N'-diisopropylcarbodiimide (DIC). This method also provides satisfactory yields and is relatively safe to use.
Chemical Structure and Biological Activity
The chemical structure of 3-(Pyrazol-1-yl)-L-alanine consists of a pyrazole ring attached to an L-alanine moiety. This unique structure contributes to its biological activity and potential therapeutic applications. The compound has been found to exhibit potent inhibitory effects on certain enzymes and receptors, making it a promising candidate for drug development. It has shown activity against various biological targets, including enzymes involved in inflammation, cancer, and neurodegenerative diseases.
Biological Effects
3-(Pyrazol-1-yl)-L-alanine has been shown to modulate cell function and signal transduction pathways. It can influence cellular processes such as proliferation, apoptosis, and differentiation. The compound's potential therapeutic effects include anti-inflammatory, anticancer, and neuroprotective properties. However, further research is needed to fully understand its mechanisms of action and potential toxic effects.
Applications
In Medical Research, 3-(Pyrazol-1-yl)-L-alanine has shown promise in drug development. It has been investigated in preclinical studies and clinical trials for its potential use in treating various diseases, including cancer and neurodegenerative disorders. The compound's benefits include its high potency and selectivity towards specific targets. However, potential side effects and toxicity need to be carefully evaluated.
In Environmental Research, 3-(Pyrazol-1-yl)-L-alanine's effects on ecosystems and its role in pollution management are areas of interest. Studies have shown its potential as a pollutant degradation agent, contributing to sustainability and environmental impact reduction. However, further research is required to assess its long-term effects on ecosystems and potential risks.
In Industrial Research, 3-(Pyrazol-1-yl)-L-alanine has been utilized in manufacturing processes to improve product quality and efficiency. Its use as a catalyst or intermediate in chemical synthesis has shown promising results. Health and safety considerations are crucial when handling this compound in industrial settings, and proper protocols should be followed to minimize risks.
Future Perspectives and Challenges
Despite the promising potential of 3-(Pyrazol-1-yl)-L-alanine, there are current limitations in its use and study. The compound's stability, bioavailability, and pharmacokinetic properties need further investigation to optimize its therapeutic potential. Challenges also include the identification of suitable drug delivery systems and the development of efficient synthesis methods.
Possible solutions and improvements involve the use of advanced drug delivery systems, such as nanoparticles or liposomes, to enhance the compound's bioavailability and target specificity. Additionally, the development of more sustainable and environmentally friendly synthesis methods is essential to reduce the compound's ecological impact.
Future trends and prospects in the application of 3-(Pyrazol-1-yl)-L-alanine in scientific research include its potential use in personalized medicine and targeted therapies. The compound's unique structure and biological activity make it a promising candidate for further exploration and development.
In conclusion, 3-(Pyrazol-1-yl)-L-alanine holds great potential in various fields, including medical, environmental, and industrial research. Its synthesis methods, chemical structure, biological activity, and applications have been discussed in this paper. Further research and advancements are needed to fully exploit its therapeutic benefits while addressing safety and environmental concerns.
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