H-Lys(Fmoc)-OH - 84624-28-2

H-Lys(Fmoc)-OH

Catalog Number: EVT-250457
CAS Number: 84624-28-2
Molecular Formula: C21H24N2O4
Molecular Weight: 368,44 g/mole
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Product Introduction

Description
H-Lys(Fmoc)-OH is a chemical compound that is widely used in scientific research, particularly in the fields of medicine, environmental science, and industry. This paper aims to provide an overview of the synthesis, chemical structure, biological activity, and applications of H-Lys(Fmoc)-OH, as well as its potential future perspectives and challenges.
Applications in Various Fields
H-Lys(Fmoc)-OH has a wide range of applications in scientific research, including its use in drug development, clinical trials, and environmental research. In medical research, H-Lys(Fmoc)-OH has been shown to have potential as a therapeutic agent for the treatment of cancer, as well as other diseases such as Alzheimer's and Parkinson's. In environmental research, H-Lys(Fmoc)-OH has been used to study the effects of pollutants on ecosystems, as well as to develop new methods for pollution management and sustainability. In industrial research, H-Lys(Fmoc)-OH has been used to improve product quality and efficiency, as well as to ensure health and safety considerations in manufacturing processes.

Properties

CAS Number

84624-28-2

Product Name

H-Lys(Fmoc)-OH

IUPAC Name

(2S)-2-amino-6-(9H-fluoren-9-ylmethoxycarbonylamino)hexanoic acid

Molecular Formula

C21H24N2O4

Molecular Weight

368,44 g/mole

InChI

InChI=1S/C21H24N2O4/c22-19(20(24)25)11-5-6-12-23-21(26)27-13-18-16-9-3-1-7-14(16)15-8-2-4-10-17(15)18/h1-4,7-10,18-19H,5-6,11-13,22H2,(H,23,26)(H,24,25)/t19-/m0/s1

SMILES

C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NCCCCC(C(=O)O)N
Method of Synthesis or Extraction
H-Lys(Fmoc)-OH can be synthesized using a variety of methods, including solid-phase peptide synthesis, solution-phase peptide synthesis, and Fmoc-based peptide synthesis. Each method has its own advantages and disadvantages in terms of efficiency, yield, and environmental and safety considerations. Solid-phase peptide synthesis is the most commonly used method for synthesizing H-Lys(Fmoc)-OH, as it allows for the production of high-quality peptides with high yields and minimal environmental impact.
Chemical Structure and Biological Activity
H-Lys(Fmoc)-OH is a peptide that consists of a lysine residue with a fluorenylmethyloxycarbonyl (Fmoc) protecting group attached to the amino group. The Fmoc group can be removed using a base such as piperidine, which exposes the amino group for further chemical reactions. H-Lys(Fmoc)-OH has been shown to have potent biological activity, particularly in its ability to inhibit the growth of cancer cells by inducing apoptosis.
Biological Effects
H-Lys(Fmoc)-OH has been shown to have a variety of effects on cell function and signal transduction, including the inhibition of cell proliferation, the induction of apoptosis, and the modulation of gene expression. It has also been shown to have potential therapeutic effects in the treatment of cancer, as well as potential toxic effects at high doses.
Future Perspectives and Challenges
Despite its many potential applications, there are still limitations in the use and study of H-Lys(Fmoc)-OH, particularly in terms of its toxicity and potential side effects. Future research will need to focus on developing new methods for synthesizing and using H-Lys(Fmoc)-OH that are more efficient, safe, and environmentally friendly. Additionally, there is a need for further research into the potential therapeutic and toxic effects of H-Lys(Fmoc)-OH, as well as its role in environmental and industrial research. Overall, H-Lys(Fmoc)-OH has the potential to be a valuable tool in scientific research, but further research is needed to fully understand its potential and limitations.

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