68684-55-9, 四水合硫胺焦磷酸酯,
Thiamine Diphosphoric Acid Ester Ttetrahydrate,
CAS: 68684-55-9
C12H18N4O7P2S·4H2O / 496.37
MFCD00150680
Cocarboxylase tetrahydrate is a pharmaceutical preparation that contains vitamin D3, pyridoxine hydrochloride, and sodium cocarboxylase. Vitamin D3 is involved in the absorption of calcium and phosphorus from food into the blood and its metabolism by the liver. Pyridoxine hydrochloride (vitamin B6) is involved in amino acid metabolism, brain function, and red blood cell formation. Sodium cocarboxylase has been used as a treatment for constipation due to its ability to stimulate the intestines. Cocarboxylase tetrahydrate has been shown to have clinical use in subcutaneous tissue for treating wounds such as burns and ulcers. It works by converting inactive carboxylic acids into active ones that can be utilized by the body. Cocarboxylase tetrahydrate also prevents or reverses dehydration by increasing fluid retention and electrolyte balance in the body.
Cocarboxylase is an essential coenzyme that plays a crucial role in numerous biological processes such as energy metabolism, neurotransmitter synthesis, and gene expression. It is a water-soluble derivative of vitamin B1 (thiamin) and is involved in various enzymatic reactions. The purpose of this paper is to provide an overview of cocarboxylase, including its definition and background, physical and chemical properties, synthesis, 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:
Cocarboxylase is a coenzyme that works together with enzymes to catalyze biochemical reactions in the body. It is also known as thiamin diphosphate or thiamin pyrophosphate. The coenzyme was first discovered by the German chemist, Thiamine, in 1936. Cocarboxylase is synthesized from thiamin through an enzymatic conversion process catalyzed by thiamin pyrophosphokinase.
Synthesis and Characterization:
Cocarboxylase is synthesized from thiamin through an enzymatic conversion process catalyzed by thiamin pyrophosphokinase. The synthesis of cocarboxylase involves the phosphorylation of thiamin with ATP to form thiamin pyrophosphate, which then reacts with magnesium ions to form cocarboxylase. The characterization of cocarboxylase is mainly done using spectroscopic techniques such as UV spectrophotometry, infrared spectroscopy, and nuclear magnetic resonance.
Analytical Methods:
Various analytical methods have been established to measure cocarboxylase levels in biological specimens. These methods include HPLC, colorimetric assays, enzymatic assays, and radioimmunoassays. These analytical methods are used to determine the concentration of cocarboxylase in biological samples such as blood, plasma, and urine.
Biological Properties:
Cocarboxylase plays a significant role in biological processes such as energy metabolism, neurotransmitter synthesis, and gene expression. Cocarboxylase is involved in the catalysis of key enzymes such as pyruvate dehydrogenase, α-ketoglutarate dehydrogenase, and branched-chain α-keto acid dehydrogenase. These enzymes are essential for energy metabolism and are involved in the conversion of pyruvate to acetyl-CoA, which enters the Krebs cycle. Cocarboxylase is also required for the biosynthesis of neurotransmitters, which are crucial for proper brain function.
Toxicity and Safety in Scientific Experiments:
Cocarboxylase is generally considered safe and non-toxic, as it is a naturally occurring compound in the human body. However, in high doses, it may cause adverse effects such as nausea, vomiting, and headache. It is important to note that there is no evidence of long-term toxicity associated with cocarboxylase.
Applications in Scientific Experiments:
Cocarboxylase has various applications in scientific experiments, including therapeutic uses in metabolic disorders, research in enzyme kinetics, and therapeutic applications in neurodegenerative diseases. Cocarboxylase can be used to treat metabolic disorders such as beriberi, which is caused by thiamin deficiency. It is also used to study the kinetics of enzymes that depend on cocarboxylase as a cofactor. Cocarboxylase has also been used in the treatment of neurodegenerative diseases such as Alzheimer's disease.
Current State of Research:
The current state of research on cocarboxylase is focused on understanding the mechanisms and effects of its enzymatic reactions. Studies have also been conducted on the use of cocarboxylase in the treatment of various diseases such as diabetes, neurodegenerative diseases, and metabolic disorders. There is also research being done on the development of novel analytical methods for measuring cocarboxylase levels in biological samples.
Potential Implications in Various Fields of Research and Industry:
Cocarboxylase has potential implications in various fields of research and industry such as medicine, biochemistry, and nutrition. It can be used in the treatment of various diseases such as metabolic disorders and neurodegenerative diseases. Cocarboxylase can also be used in the development of diagnostic tests for thiamin deficiency. Additionally, cocarboxylase can be used in the food industry as a nutritional supplement in food fortification.
Limitations and Future Directions:
One of the limitations of cocarboxylase is its poor solubility, which limits its use in scientific experiments. Future research should focus on the development of more soluble forms of cocarboxylase. Additionally, research should focus on understanding the mechanisms and effects of cocarboxylase in various diseases. Future research should also focus on the development of novel analytical methods for measuring cocarboxylase levels in biological samples. Finally, there is a need for more research on the potential implications of cocarboxylase in various fields of research and industry.
Conclusion:
In conclusion, cocarboxylase is an essential coenzyme that plays a critical role in various biological processes such as energy metabolism and neurotransmitter synthesis. Cocarboxylase has potential applications in various fields of research and industry, including the treatment of metabolic disorders and neurodegenerative diseases. However, there are limitations to cocarboxylase, such as poor solubility. Future research should focus on developing more soluble forms of cocarboxylase and understanding the mechanisms and effects of cocarboxylase in various diseases.
CAS Number | 68684-55-9 |
Product Name | Cocarboxylase |
IUPAC Name | [2-[3-[(4-amino-2-methylpyrimidin-5-yl)methyl]-4-methyl-1,3-thiazol-3-ium-5-yl]ethoxy-hydroxyphosphoryl] hydrogen phosphate;tetrahydrate |
Molecular Formula | C12H18N4O7P2S 4H2O |
Molecular Weight | 496.37 |
InChI | InChI=1S/C12H18N4O7P2S.4H2O/c1-8-11(3-4-22-25(20,21)23-24(17,18)19)26-7-16(8)6-10-5-14-9(2)15-12(10)13;;;;/h5,7H,3-4,6H2,1-2H3,(H4-,13,14,15,17,18,19,20,21);4*1H2 |
SMILES | CC1=C(SC=[N+]1CC2=CN=C(N=C2N)C)CCOP(=O)(O)OP(=O)(O)[O-].O.O.O.O |
Synonyms | Thiamine diphosphoric acid ester |
COA:
Name: Thiamine Diphosphoric Acid Ester Ttetrahydrate or Cocarboxylase Tetrahydrate
CAS: 68684-55-9 M.F.: C12H18N4O7P2S.4H2O M.W.:496.37
Items | Standards | Results |
Appearance | White crystalline powder | Complies |
Solubility | Easily soluble in water, insoluble in general organic solvent | Complies |
Identification | IR and HPLC | Complies |
pH (10%) | 2 - 4 | 3.1 |
Thiamine monophosphoric acid ester | Max. 1% | 0.48% |
Other any impurity | Max. 0.5% | Complies |
Chlorides | Max. 0.1% | Complies |
Heavy metals | Max.20ppm | Complies |
Water Content | 14% - 16% | 14.6% |
Free H3PO4 | Max. 0.5% | Complies |
Assay by HPLC | Min. 98% | 99.4% |
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