Z-Ala-pro-OH - 21027-01-0

Z-Ala-pro-OH

Catalog Number: EVT-316624
CAS Number: 21027-01-0
Molecular Formula: C16H20N2O5
Molecular Weight: 320.34 g/mol
The product is for non-human research only. Not for therapeutic or veterinary use.
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Product Introduction

Description
Z-Ala-pro-OH is a dipeptide consisting of alanine and proline, with a Z configuration at the N-terminal amino group. It is a commonly used peptide in medical, environmental, and industrial research due to its unique chemical structure and biological activity.
Applications in Various Fields
Z-Ala-pro-OH has various applications in medical, environmental, and industrial research. In medical research, it has been studied for its role in drug development, particularly in the treatment of hypertension and inflammation. Clinical trials have shown promising results, but further studies are needed to determine its safety and efficacy. In environmental research, Z-Ala-pro-OH has been studied for its effects on ecosystems and its role in pollution management. It has been shown to have potential as a natural antioxidant and may be useful in mitigating the effects of environmental pollutants. In industrial research, Z-Ala-pro-OH has been used in manufacturing processes to improve product quality and efficiency. Health and safety considerations should be taken into account when using Z-Ala-pro-OH in industrial applications.

Properties

CAS Number

21027-01-0

Product Name

Z-Ala-pro-OH

IUPAC Name

1-[2-(phenylmethoxycarbonylamino)propanoyl]pyrrolidine-2-carboxylic acid

Molecular Formula

C16H20N2O5

Molecular Weight

320.34 g/mol

InChI

InChI=1S/C16H20N2O5/c1-11(14(19)18-9-5-8-13(18)15(20)21)17-16(22)23-10-12-6-3-2-4-7-12/h2-4,6-7,11,13H,5,8-10H2,1H3,(H,17,22)(H,20,21)

InChI Key

RSSOZTMMMIWOJB-UHFFFAOYSA-N

SMILES

CC(C(=O)N1CCCC1C(=O)O)NC(=O)OCC2=CC=CC=C2

Canonical SMILES

CC(C(=O)N1CCCC1C(=O)O)NC(=O)OCC2=CC=CC=C2
Method of Synthesis or Extraction
Z-Ala-pro-OH can be synthesized using various methods, including solid-phase peptide synthesis, solution-phase peptide synthesis, and enzymatic synthesis. Solid-phase peptide synthesis is the most commonly used method, which involves the stepwise addition of protected amino acids to a solid support. Solution-phase peptide synthesis is another method that involves the coupling of protected amino acids in solution. Enzymatic synthesis involves the use of enzymes to catalyze the formation of peptide bonds. The efficiency and yield of each method depend on the specific conditions used, such as the type of protecting groups, solvents, and coupling reagents. Environmental and safety considerations should also be taken into account when choosing a method, as some methods may produce hazardous waste or require toxic reagents.
Chemical Structure and Biological Activity
Z-Ala-pro-OH has a unique chemical structure that confers specific biological activity. It has been shown to inhibit the activity of angiotensin-converting enzyme (ACE), which is involved in the regulation of blood pressure. Z-Ala-pro-OH also has antioxidant activity and can scavenge free radicals. In addition, it has been shown to have anti-inflammatory and immunomodulatory effects.
Biological Effects
Z-Ala-pro-OH has been shown to affect cell function and signal transduction in various ways. It can modulate the activity of enzymes involved in cell signaling pathways, such as protein kinases and phosphatases. It can also affect the expression of genes involved in inflammation and oxidative stress. Z-Ala-pro-OH has potential therapeutic effects in the treatment of hypertension, inflammation, and oxidative stress-related diseases. However, it may also have toxic effects at high concentrations, and further studies are needed to determine its safety and efficacy.
Future Perspectives and Challenges
Despite the promising results of studies on Z-Ala-pro-OH, there are still limitations in its use and study. One challenge is the difficulty in synthesizing large quantities of Z-Ala-pro-OH for clinical trials and industrial applications. Another challenge is the lack of understanding of its mechanism of action and potential side effects. Future research should focus on addressing these challenges and improving the synthesis and characterization of Z-Ala-pro-OH. In addition, further studies are needed to determine its safety and efficacy in clinical and industrial applications.
Conclusion:
Z-Ala-pro-OH is a dipeptide with unique chemical structure and biological activity. It has potential therapeutic effects in the treatment of hypertension, inflammation, and oxidative stress-related diseases. It also has applications in environmental and industrial research. However, further studies are needed to determine its safety and efficacy, and to address the challenges in its use and study.

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