210418-02-3, 2-O-(4-Nitrophenyl)-a-D-N-acetylneuraminic acid ammonium salt,
CAS:210418-02-3
C20H24N2O11 / 468.41
MFCD04039642
2-O-(4-Nitrophenyl)-a-D-N-acetylneuraminic acid ammonium salt is a chromogenic substrate commonly used in the detection and quantification of sialidase activity. Sialidases are a family of enzymes that hydrolyze sialic acid residues from glycoconjugates. This substrate is used to detect bacterial and viral sialidases, which play an important role in pathogen infectivity. The ammonium salt form of the substrate is preferred for its solubility in water-based assay systems.
2-O-(4-Nitrophenyl)-α-D-N-acetylneuraminic acid ammonium salt, also known as 4-nitrophenyl sialic acid (NPSA), is a synthetic compound used in various scientific experiments. In this paper, we will explore its definition, physical and chemical properties, synthesis and characterization, analytical methods, biological properties, toxicity and safety in scientific experiments, applications in scientific experiments, current state of research, potential implications in various fields of research and industry, limitations, and future directions.
Definition and Background
NPSA is a derivative of sialic acid, a type of monosaccharide that is commonly found on the surface of cells and plays a crucial role in cellular recognition and communication. NPSA is often used as a substrate for sialidases, enzymes that cleave sialic acid residues from glycoconjugates. By measuring the activity of sialidases on NPSA, researchers can gain insights into the role of sialic acid in various biological processes.
Physical and Chemical Properties
NPSA is a white crystalline powder that is soluble in water and organic solvents. Its molecular formula is C15H20N2O10 and its molecular weight is 408.32 g/mol. NPSA has a high melting point of 210-212°C and can be stored at room temperature for extended periods.
Synthesis and Characterization
NPSA can be synthesized by coupling 4-nitrophenol with a sialic acid derivative in the presence of a coupling reagent such as N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide (EDC). The resulting NPSA product can be purified by column chromatography and characterized using techniques such as nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry.
Analytical Methods
The activity of sialidases on NPSA can be measured using various analytical methods, such as high-performance liquid chromatography (HPLC) or colorimetric assays. These methods involve monitoring the release of 4-nitrophenol from NPSA by sialidases, which can be quantified using appropriate standards.
Biological Properties
NPSA has been shown to inhibit the activity of various sialidases, including those from influenza viruses and bacterial pathogens. It has also been used as a substrate to measure the activity of sialidases in various biological samples, such as cell extracts and saliva. In addition, NPSA has been employed in studies investigating the role of sialic acid in cancer metastasis and neurodegenerative diseases.
Toxicity and Safety in Scientific Experiments
While NPSA is generally considered safe for use in scientific experiments, it should be handled with care and appropriate safety measures should be taken. NPSA can cause irritation to the skin, eyes, and respiratory tract if inhaled or swallowed. Researchers should use protective equipment such as gloves, goggles, and a dust mask when handling NPSA.
Applications in Scientific Experiments
NPSA has a wide range of applications in scientific experiments, including the measurement of sialidase activity, the investigation of sialic acid function in various biological processes, and the characterization of sialic acid-binding proteins. NPSA has also been used as a tool to study the binding and specificity of lectins, proteins that recognize and bind to specific carbohydrate structures.
Current State of Research
Research on NPSA has been ongoing for several decades, with numerous studies exploring its biological properties and applications. Recent developments include the use of NPSA as a substrate for high-throughput screening of sialidase inhibitors and the development of new methods for synthesizing and characterizing NPSA derivatives.
Potential Implications in Various Fields of Research and Industry
NPSA and its derivatives have potential implications in various fields of research and industry, including drug discovery, biotechnology, and glycobiology. NPSA can be used to screen for new sialidase inhibitors, which could lead to the development of new treatments for viral and bacterial infections. In addition, NPSA and its derivatives can be used to study the interactions between sialic acid and proteins, which could lead to the development of new therapeutic agents targeting these interactions.
Limitations and Future Directions
One limitation of NPSA is that it is not found naturally in biological systems, which may limit its relevance in certain studies. In addition, NPSA only represents a single sialic acid residue, whereas naturally occurring sialic acids can have various modifications and linker structures. Future directions in NPSA research include the development of new synthetic methods for producing NPSA derivatives with more diverse sialic acid structures and the identification of new applications for NPSA and its derivatives in various fields of research and industry.
Some potential future directions could include the development of new methods for measuring sialidase activity using NPSA derivatives, the identification of new sialic acid-binding proteins using NPSA derivatives as probes, and the exploration of the potential therapeutic applications of NPSA derivatives in various diseases. Furthermore, NPSA derivatives could be used to understand the structural basis for interactions between sialic acid and proteins, which could be useful in developing new therapeutic agents for these interactions.
In conclusion, NPSA is a synthetic compound with a wide range of applications in scientific research. Its physical and chemical properties, synthesis and characterization, analytical methods, biological properties, toxicity and safety in scientific experiments, applications in scientific experiments, current state of research, potential implications in various fields of research and industry, limitations and future directions have been discussed in this paper. NPSA and its derivatives continue to be valuable tools for studying the role of sialic acid in various biological processes and for developing new therapeutic agents targeting sialic acid-related interactions.
CAS Number | 210418-02-3 |
Product Name | 2-O-(4-Nitrophenyl)-a-D-N-acetylneuraminic acid ammonium salt |
IUPAC Name | azanium;(2S,4S,5R,6R)-5-acetamido-4-hydroxy-2-(4-nitrophenoxy)-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylate |
Molecular Formula | C17H25N3O11 |
Molecular Weight | 447.4 g/mol |
InChI | InChI=1S/C17H22N2O11.H3N/c1-8(21)18-13-11(22)6-17(16(25)26,30-15(13)14(24)12(23)7-20)29-10-4-2-9(3-5-10)19(27)28;/h2-5,11-15,20,22-24H,6-7H2,1H3,(H,18,21)(H,25,26);1H3/t11-,12+,13+,14+,15+,17+;/m0./s1 |
InChI Key | XTRDXLWOELJKNO-MLFSYFRJSA-N |
SMILES | CC(=O)NC1C(CC(OC1C(C(CO)O)O)(C(=O)[O-])OC2=CC=C(C=C2)[N+](=O)[O-])O.[NH4+] |
Canonical SMILES | CC(=O)NC1C(CC(OC1C(C(CO)O)O)(C(=O)[O-])OC2=CC=C(C=C2)[N+](=O)[O-])O.[NH4+] |
Isomeric SMILES | CC(=O)N[C@@H]1[C@H](C[C@@](O[C@H]1[C@@H]([C@@H](CO)O)O)(C(=O)[O-])OC2=CC=C(C=C2)[N+](=O)[O-])O.[NH4+] |
CAS No: 13264-91-0,210418-02-3 Synonyms: o-Nitrophenyl 2-acetamido-2-deoxy-a-D-glucopyranoside triacetateo-Nitrophenyl 2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-a-D-glucopyranoside MDL No: MFCD04039642 Chemical Formula: C20H24N2O11 Molecular Weight: 468.41 |
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