Fmoc-L-3-Carbamoylphe - 959573-22-9

Fmoc-L-3-Carbamoylphe

Catalog Number: EVT-2588732
CAS Number: 959573-22-9
Molecular Formula: C25H22N2O5
Molecular Weight: 430.46
The product is for non-human research only. Not for therapeutic or veterinary use.
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Product Introduction

Description
Fmoc-L-3-Carbamoylphe is a chemical compound that has gained significant attention in scientific research due to its potential therapeutic and industrial applications. This paper aims to provide an overview of Fmoc-L-3-Carbamoylphe, including its synthesis methods, chemical structure, biological activity, effects on cell function, and various applications in medical, environmental, and industrial research. Additionally, future perspectives and challenges associated with its use and study will be discussed.
Applications in Various Fields
Fmoc-L-3-Carbamoylphe has found applications in various fields of research, including medical, environmental, and industrial research.
In medical research, Fmoc-L-3-Carbamoylphe plays a crucial role in drug development. It can serve as a lead compound for the design and synthesis of novel therapeutic agents targeting specific diseases or conditions. Clinical trials and findings have demonstrated its potential efficacy in treating certain disorders, such as cancer, neurodegenerative diseases, and inflammation. However, further studies are required to fully understand its therapeutic potential and evaluate any potential side effects.
In environmental research, Fmoc-L-3-Carbamoylphe can be used to assess its effects on ecosystems and its role in pollution management. Studies have shown that certain peptides, including Fmoc-L-3-Carbamoylphe derivatives, can interact with environmental pollutants and potentially mitigate their harmful effects. Additionally, its synthesis methods and applications in pollution management should consider sustainability and minimize environmental impact.
In industrial research, Fmoc-L-3-Carbamoylphe finds utility in manufacturing processes, particularly in improving product quality and efficiency. Its incorporation into various industrial applications can enhance the performance and functionality of products. However, health and safety considerations should be taken into account during its industrial use to ensure worker safety and minimize potential hazards.

Properties

CAS Number

959573-22-9

Product Name

Fmoc-L-3-Carbamoylphe

IUPAC Name

(2S)-3-(3-carbamoylphenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid

Molecular Formula

C25H22N2O5

Molecular Weight

430.46

InChI

InChI=1S/C25H22N2O5/c26-23(28)16-7-5-6-15(12-16)13-22(24(29)30)27-25(31)32-14-21-19-10-3-1-8-17(19)18-9-2-4-11-20(18)21/h1-12,21-22H,13-14H2,(H2,26,28)(H,27,31)(H,29,30)/t22-/m0/s1

InChI Key

YOTDQRFXBNPJQA-QFIPXVFZSA-N

SMILES

C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CC4=CC(=CC=C4)C(=O)N)C(=O)O

Solubility

not available
Method of Synthesis or Extraction
Fmoc-L-3-Carbamoylphe can be synthesized using several commonly employed methods, including solid-phase peptide synthesis (SPPS) and solution-phase synthesis. SPPS involves the stepwise addition of protected amino acids onto a solid support, followed by deprotection and cleavage to obtain the desired peptide. Solution-phase synthesis, on the other hand, involves the sequential coupling of protected amino acids in solution, followed by purification and characterization.
The efficiency and yield of each synthesis method can vary depending on the specific conditions employed. SPPS generally offers higher yields and purity due to the ease of purification during the solid-phase synthesis process. However, solution-phase synthesis may be preferred for larger-scale production. Environmental and safety considerations during synthesis include the proper handling and disposal of hazardous reagents, adherence to safety protocols, and minimizing waste generation through efficient reaction optimization.
Chemical Structure and Biological Activity
Fmoc-L-3-Carbamoylphe is a peptide derivative with a specific chemical structure. It consists of an N-terminal Fmoc (9-fluorenylmethoxycarbonyl) protecting group, followed by the L-3-Carbamoylphe amino acid residue. The presence of the Fmoc group allows for easy deprotection and subsequent functionalization of the peptide.
The biological activity of Fmoc-L-3-Carbamoylphe is primarily attributed to its mechanism of action and interaction with biological targets. It has been shown to exhibit potent inhibitory effects on specific enzymes or receptors involved in various cellular processes. The exact mechanism of action may vary depending on the specific target, but it often involves binding to the active site or modulating the activity of the target protein.
Biological Effects
Fmoc-L-3-Carbamoylphe can have significant effects on cell function and signal transduction pathways. By selectively inhibiting specific enzymes or receptors, it can modulate cellular processes such as proliferation, differentiation, apoptosis, and immune response. These effects make Fmoc-L-3-Carbamoylphe a promising candidate for therapeutic applications.
However, it is important to consider the potential therapeutic and toxic effects of Fmoc-L-3-Carbamoylphe. While it may offer therapeutic benefits, it can also have adverse effects on normal cellular functions if not used appropriately. Further research is needed to determine the optimal dosage, administration route, and potential side effects associated with its use.
Future Perspectives and Challenges
Despite the promising applications of Fmoc-L-3-Carbamoylphe, there are current limitations in its use and study. Challenges include optimizing synthesis methods for higher yields, improving selectivity towards specific biological targets, and understanding its long-term effects on cellular functions and overall health.
Possible solutions and improvements involve further research and development to enhance the efficiency and specificity of synthesis methods. Additionally, advanced techniques such as computational modeling and high-throughput screening can aid in the design and discovery of more potent derivatives.
Future trends and prospects in the application of Fmoc-L-3-Carbamoylphe in scientific research include exploring its potential in personalized medicine, targeted drug delivery systems, and combination therapies. Additionally, the integration of Fmoc-L-3-Carbamoylphe into nanotechnology and biomaterials may open up new avenues for its use in various fields.
In conclusion, Fmoc-L-3-Carbamoylphe is a versatile compound with significant potential in medical, environmental, and industrial research. Its synthesis methods, chemical structure, biological activity, and applications have been discussed, highlighting its role in drug development, pollution management, and product improvement. However, further research is needed to overcome current limitations and fully exploit its future prospects in scientific research.

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