18423-42-2, Cytidine-5-triphosphoric acid disodium salt,
三磷酸胞苷二钠,
CAS:18423-42-2
C9H14N3Na2O14P3 / 527.12
Cytidine-5'-triphosphoric acid disodium salt is an unassigned compound that is a potent inhibitor of protein synthesis. It has been shown to have a specific growth rate of 0.0003, which is significantly lower than the growth rate for other tested compounds. Cytidine-5'-triphosphoric acid disodium salt also inhibits the growth of Klebsiella aerogenes, Escherichia coli, and Enterococcus faecalis at concentrations as low as 1 ppm. The compound has been found to be hydraulically resistant and can be used in polyolefin formulations with high resistance to organic solvents. Cytidine-5'-triphosphoric acid disodium salt is also used as a supplement in the production of proteins such as enzymes, antibodies, hormones, and cytokines because it blocks the formation of proteins by interfering with ribosomes and preventing them from binding to mRNA transcripts.
Cytidine 5'-(tetrahydrogen triphosphate), sodium salt (CTP) is a key nucleotide that plays a crucial role in various biological processes. It is synthesized in the body via various pathways and has several chemical and physical properties that make it an essential component of the cell. In this paper, we will discuss the definition and background of CTP, 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.
Definition and Background
CTP is a nucleotide that is composed of a nucleoside (cytidine) and three phosphate groups. It is a precursor molecule for RNA synthesis, and its deoxy form (dCTP) is an essential building block for DNA synthesis. It is also involved in energy transfer and cell signaling pathways. The sodium salt form of CTP is more stable and has better solubility properties than the free acid form.
Physical and Chemical Properties
CTP is a white or off-white powder that is soluble in water and slightly soluble in ethanol. Its melting point is around 210-212°C. It has a pH of around 7.5-8.0 in water. CTP is a highly polar molecule due to the presence of multiple phosphate groups. It is relatively stable under normal conditions but can be easily hydrolyzed by strong acids or alkalis.
Synthesis and Characterization
CTP can be synthesized in the body via various pathways, including the de novo biosynthesis pathway, the salvage pathway, and the salvage pathway via the deaminated bases. The de novo pathway involves the conversion of ribose-5-phosphate and other precursors into CTP via various enzymatic reactions. In the salvage pathway, preformed nucleotides (such as uridine) are salvaged and converted into CTP via a series of enzymatic reactions. The deaminated base salvage pathway involves the conversion of deaminated nucleotides (such as uracil or hypoxanthine) into CTP via the salvage pathway.
The synthesis and purification of CTP can also be achieved via chemical methods. For example, CTP can be synthesized via the reaction of cytidine with tripolyphosphoric acid. The purified product can be characterized using various analytical methods, such as HPLC, NMR, and mass spectrometry.
Analytical Methods
Various analytical methods can be used to detect and quantify CTP in biological samples and experimental settings. These include high-performance liquid chromatography (HPLC), capillary electrophoresis, mass spectrometry, and enzymatic assays. HPLC is the most commonly used method for CTP quantification, as it allows for rapid and accurate analysis of CTP levels in different biological samples.
Biological Properties
CTP plays several critical roles in biological systems. It is an essential precursor for RNA and DNA synthesis, as well as for the production of phosphatidylcholine and other membrane phospholipids. It is also involved in energy transfer and cell signaling pathways. Furthermore, CTP has been shown to play a critical role in the regulation of gene expression and cell cycle progression.
Toxicity and Safety in Scientific Experiments
CTP is generally considered safe and non-toxic in scientific experiments when used at appropriate concentrations. However, high doses of CTP may have adverse effects on cell viability and can disrupt cellular processes. It is essential to ensure that CTP is used at appropriate concentrations in experiments to avoid toxicity and safety concerns.
Applications in Scientific Experiments
CTP has a wide range of applications in scientific experiments. It can be used as a substrate in enzymatic assays to measure the activity of various nucleotide-metabolizing enzymes. It can also be used as a precursor for RNA and DNA synthesis in cell-free systems. Furthermore, CTP has been used as an energy donor for metabolic labeling and tagging experiments.
Current State of Research
Research on CTP is ongoing, with a focus on understanding its biological functions and potential therapeutic applications. Recent studies have shown that CTP plays a crucial role in regulating gene expression and cellular processes. Furthermore, CTP has been implicated in various diseases, including cancer and viral infections. Research is currently focused on understanding the mechanisms underlying these effects and developing novel therapeutic strategies based on CTP.
Potential Implications in Various Fields of Research and Industry
CTP has several potential implications in various fields of research and industry. For example, CTP-based therapies may have applications in cancer treatment, where they could be used to selectively target cancer cells or to modulate gene expression. Furthermore, CTP-based metabolic labeling and tagging methods could have applications in drug discovery and development.
Limitations and Future Directions
Although CTP has several potential applications in science and industry, there are also some limitations that need to be addressed. For example, the use of CTP in therapeutic applications may be limited by its toxicity at high doses. Furthermore, the mechanisms underlying CTP's effects on various cellular processes are not yet fully understood.
Future research is needed to address these limitations and to further explore the potential applications of CTP. Potential directions include developing new methods for the synthesis and purification of CTP, exploring the role of CTP in various biological processes, and developing novel therapeutic strategies based on CTP.
CAS Number | 18423-42-2 |
Product Name | Cytidine 5'-(tetrahydrogen triphosphate), sodium salt |
IUPAC Name | sodium;[[[(2R,3S,4R)-5-(4-amino-2-oxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl] hydrogen phosphate |
Molecular Formula | C9H14N3Na2O14P3 |
Molecular Weight | 527.12 g/mol |
InChI | InChI=1S/C9H16N3O14P3.Na/c10-5-1-2-12(9(15)11-5)8-7(14)6(13)4(24-8)3-23-28(19,20)26-29(21,22)25-27(16,17)18;/h1-2,4,6-8,13-14H,3H2,(H,19,20)(H,21,22)(H2,10,11,15)(H2,16,17,18);/q;+1/p-1/t4-,6-,7-,8?;/m1./s1 |
InChI Key | WLXAPABOZXFQTH-YMCBRKDHSA-M |
SMILES | C1=CN(C(=O)N=C1N)C2C(C(C(O2)COP(=O)(O)OP(=O)(O)OP(=O)(O)[O-])O)O.[Na+] |
Canonical SMILES | C1=CN(C(=O)N=C1N)C2C(C(C(O2)COP(=O)(O)OP(=O)(O)OP(=O)(O)[O-])O)O.[Na+] |
Isomeric SMILES | C1=CN(C(=O)N=C1N)C2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)OP(=O)(O)OP(=O)(O)[O-])O)O.[Na+] |
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