Fmoc-L-Styrylalanine - 159610-82-9

Fmoc-L-Styrylalanine

Catalog Number: EVT-1485017
CAS Number: 159610-82-9
Molecular Formula: C26H23NO4
Molecular Weight: 413.47
The product is for non-human research only. Not for therapeutic or veterinary use.
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Product Introduction

Description
Fmoc-L-Styrylalanine is a modified amino acid that has gained significant attention in recent years due to its unique chemical structure and potential biological activity. This paper aims to provide an overview of the synthesis, chemical structure, biological activity, and applications of Fmoc-L-Styrylalanine in various fields of research.
Applications in Various Fields
Fmoc-L-Styrylalanine has potential applications in various fields of research, including medical, environmental, and industrial research. In medical research, it has been studied for its role in drug development, and some clinical trials have shown promising results in the treatment of certain cancers. However, more research is needed to determine its safety and efficacy in humans. In environmental research, Fmoc-L-Styrylalanine has been studied for its effects on ecosystems and its potential role in pollution management. In industrial research, it has been used in manufacturing processes to improve product quality and efficiency, but health and safety considerations must be taken into account.

Properties

CAS Number

159610-82-9

Product Name

Fmoc-L-Styrylalanine

IUPAC Name

(E,2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-5-phenylpent-4-enoic acid

Molecular Formula

C26H23NO4

Molecular Weight

413.47

InChI

InChI=1S/C26H23NO4/c28-25(29)24(16-8-11-18-9-2-1-3-10-18)27-26(30)31-17-23-21-14-6-4-12-19(21)20-13-5-7-15-22(20)23/h1-15,23-24H,16-17H2,(H,27,30)(H,28,29)/b11-8+/t24-/m0/s1

SMILES

C1=CC=C(C=C1)C=CCC(C(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24
Method of Synthesis or Extraction
Fmoc-L-Styrylalanine 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 resin-bound peptide chain. The efficiency and yield of each method depend on several factors, such as the type of protecting groups used, the reaction conditions, and the purity of the starting materials. Environmental and safety considerations are also important factors to consider during the synthesis process, as some reagents and solvents used in the process can be hazardous to the environment and human health.
Chemical Structure and Biological Activity
Fmoc-L-Styrylalanine is a modified amino acid that contains a styryl group attached to the side chain of L-alanine. The styryl group imparts unique chemical and biological properties to the molecule, making it a potential candidate for various applications. The mechanism of action and biological targets of Fmoc-L-Styrylalanine are not fully understood, but studies have shown that it exhibits bioactivity and potency against certain cancer cell lines and bacteria.
Biological Effects
Fmoc-L-Styrylalanine has been shown to affect cell function and signal transduction in various ways. It has been reported to induce apoptosis in cancer cells, inhibit bacterial growth, and modulate immune responses. However, the potential therapeutic and toxic effects of Fmoc-L-Styrylalanine are still under investigation, and more research is needed to fully understand its biological effects.
Future Perspectives and Challenges
Despite the potential applications of Fmoc-L-Styrylalanine, 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 biological targets. Additionally, the safety and efficacy of Fmoc-L-Styrylalanine in humans need to be further investigated before it can be used as a therapeutic agent. However, with the advancement of technology and the increasing interest in modified amino acids, Fmoc-L-Styrylalanine holds promise for future research and applications in various fields.

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