1 2 Deoxy 2 Fluoro Beta D Arabinofuranosyl 5 Iodouracil
Iodobenzene

1-(2-deoxy-2-fluoro-.beta.-d-arabinofuranosyl)-5-iodouracil

Fengxi Chemical

Specifications

HS Code

325690

Chemical Name 1-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-5-iodouracil
Molecular Formula C9H11FIN2O5
Molecular Weight 366.098 g/mol
Appearance White to off - white solid
Melting Point Approximately 190 - 195°C
Solubility Slightly soluble in water, soluble in organic solvents like DMSO
Pka Around 9.2
Structure Type Nucleoside analog
Biological Activity Antiviral, inhibits viral DNA synthesis
Stability Stable under normal storage conditions in dry and cool place
Name 1-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-5-iodouracil
Chemical Formula C9H11FIN2O5
Molecular Weight 366.1
Appearance White to off - white solid
Melting Point Approximately 175 - 177 °C
Solubility Slightly soluble in water
Pka Approx. 9.0
Logp -1.7
Cas Number 2140-71-6
Category Nucleoside analog
Pharmaceutical Use Antiviral agent
Chemical Name 1-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-5-iodouracil
Molecular Formula C9H11FIN2O5
Molecular Weight 366.099 g/mol
Appearance White to off - white solid
Melting Point 168 - 170 °C
Solubility Slightly soluble in water
Pka Approx. 9.4
Logp -2.44
Pharmaceutical Class Antiviral agent
Mechanism Of Action Inhibits viral DNA synthesis
Cas Number 69655 - 05 - 6
Chemical Name 1-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-5-iodouracil
Molecular Formula C9H11FIN2O5
Molecular Weight 366.097 g/mol
Appearance White to off - white powder
Melting Point 167 - 170 °C
Solubility Slightly soluble in water
Pka 3.9 (approximate value for the uracil moiety)
Logp - 1.3 (estimated)
Chemical Structure Type Nucleoside analog
Main Function Antiviral agent, used in treatment of certain viral infections
Packing & Storage
Packing 10 grams of 1-(2 - deoxy - 2 - fluoro - β -D - arabinofuranosyl)-5 - iodouracil in sealed chemical - grade vial.
Storage 1-(2 - deoxy - 2 - fluoro - β - d - arabinofuranosyl)-5 - iodouracil should be stored in a cool, dry place, away from direct sunlight. It is advisable to keep it in a tightly sealed container to prevent exposure to moisture and air, which could potentially degrade the chemical. Storage in a refrigerator at a controlled temperature, around 2 - 8 °C, might be optimal for long - term preservation.
Shipping 1-(2 - deoxy - 2 - fluoro - β -D - arabinofuranosyl)-5 - iodouracil is shipped with strict adherence to chemical transport regulations. Packaged securely in suitable containers, it's transported by carriers experienced in handling such chemicals.
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1-(2-deoxy-2-fluoro-.beta.-d-arabinofuranosyl)-5-iodouracil 1-(2-deoxy-2-fluoro-.beta.-d-arabinofuranosyl)-5-iodouracil 1-(2-deoxy-2-fluoro-.beta.-d-arabinofuranosyl)-5-iodouracil
General Information
Frequently Asked Questions
What is the chemical structure of 1- (2-deoxy-2-fluoro-.beta. -d-arabinofuranosyl) -5-iodouracil?
1 - (2 - deoxy - 2 - fluoro - β - D - arabinofuranosyl) - 5 - iodouracil, an organic compound, is of great significance in the field of medicinal chemistry. Its chemical structure is based on the backbone of pyrimidine compounds, which is composed of many key parts.
First, look at the uracil part, which is a nitrogen-containing heterocyclic structure and is the core infrastructure of the compound. Uridine is a member of the pyrimidine base family and plays a key role in nucleic acid biosynthesis and metabolism. In 1 - (2 - deoxy - 2 - fluoro - β - D - arabinofuranosyl) - 5 - iodouracil, uracil provides a basic check point and chemical activity center for linking to other groups.
Look at the 2 - deoxy - 2 - fluoro - β - D - arabinofuranosyl moiety, which is specifically modified to be linked to uracil. "2 - deoxy" means that the hydroxyl group on the second carbon atom of the sugar ring is replaced by a hydrogen atom. This structural change has a significant impact on the biological activity and metabolic properties of the compound. " 2-Fluorine "indicates the introduction of fluorine atoms into the second carbon atom of the sugar ring. Fluorine atoms can significantly change the lipophilicity, stability and interaction with biological targets of compounds due to their strong electronegativity and small atomic radius. The configuration of β-D-arabinofuran glycosyl determines the spatial structure and stereochemical characteristics of the whole compound, and is crucial for its binding specificity to receptors or enzymes in organisms.
Finally, there is the 5-iodine part, and the iodine atom is attached to the 5th position of the uracil ring. The large atomic radius and unique electron cloud distribution of iodine atoms endow compounds with special physical and chemical properties, which not only affect their intermolecular forces, but also change the electron cloud density distribution of compounds, which in turn affect their chemical reactivity and biological activity.
In short, the chemical structure of 1- (2-deoxy-2-fluoro - β - D-arabinofuranosyl) -5-iodouracil, through the synergistic action of uracil, modified sugar groups and iodine atoms, exhibits unique physical, chemical and biological activity characteristics, laying the foundation for its application in drug development and other fields.
What are the main uses of 1- (2-deoxy-2-fluoro-.beta.-d-arabinofuranosyl) -5-iodouracil?
1 - (2 - deoxy - 2 - fluoro - β - D - arabinofuranosyl) - 5 - iodouracil, often known by its abbreviation FIAU. This drug is mainly used in the field of antiviral, especially in the exploration of anti-hepatitis B virus.
In the past, doctors and pharmacists hoped to use the power of FIAU to overcome the stubborn disease of hepatitis B. The principle is that the substance can mimic natural nucleosides and incorporate them into the replication process of viral DNA, thereby blocking the reproduction of viruses. However, it backfired. In clinical trials, although FIAU showed some antiviral activity, it was accompanied by serious adverse reactions, and many patients suffered from life-threatening conditions such as liver failure.
In view of this serious consequence, FIAU was not widely used in clinical treatment of hepatitis B. Although its antiviral ideas are innovative, safety risks cannot be ignored. Since then, the medical community has also learned from the lessons of FIAU. When developing new drugs, it has been more cautious in safety assessment, and strives to find antiviral drugs with both efficacy and safety.
What is the market outlook for 1- (2-deoxy-2-fluoro-.beta. -d-arabinofuranosyl) -5-iodouracil?
1 - (2 - deoxy - 2 - fluoro - β - D - arabinofuranosyl) - 5 - iodouracil, its shape is specific, in the field of medicine, the prospect can not be ignored.
This substance is in the genus of antimalarial and antiviral, and has been studied many times. Past investigations have shown that it has the ability to inhibit specific malaria parasites and viruses. However, if you want to enter the market, you still need to pass many barriers.
First, the study of pharmacology and toxicology needs to be deep and comprehensive. It is necessary to carefully investigate its action path, metabolism, and potential side effects in organisms. If you don't know this, use it rashly, or cause unbearable consequences.
For the second time, the preparation process is also a priority. The drug must have good dissolution and stability in order to ensure the good efficacy of the drug. If the preparation is not good, even if the effective ingredients are excellent, it is difficult to develop its ability.
Furthermore, clinical trials are a crucial step. It is necessary to go through multiple phase trials and collect data from different populations to prove that it is safe and effective before it can be approved for market entry.
From the current perspective, 1 - (2 - deoxy - 2 - fluoro - β - D - arabinofuran) - 5 - iodouracil has potential, but there is still a long way to go before it can become a commercially available drug. It requires unremitting research by scientific researchers to solve all kinds of problems.
What is the production process of 1- (2-deoxy-2-fluoro-.beta. -d-arabinofuranosyl) -5-iodouracil?
1-%282-deoxy-2-fluoro-. Beta.-d-arabinofuranosyl%29-5-iodouracil is 1- (2-deoxy-2-fluoro-β-D-arabinofuranosyl) -5-iodouracil, the preparation process is as follows:
First take an appropriate amount of starting material, this raw material needs to have a specific chemical structure, in order to lay the foundation for the subsequent reaction. The starting material is placed in the reaction kettle, and an appropriate amount of reaction solvent is added to make the raw material evenly dispersed in it, so that the reaction can be fully carried out. The choice of reaction solvent must conform to the characteristics of the raw material and the reaction conditions to ensure the smooth progress of the reaction.
Then, specific reagents and catalysts are added to the reaction system one after another. The dosage and order of addition of the reagents must be precisely controlled, and a slight difference may cause a deviation in the reaction. The function of the catalyst is to accelerate the reaction process and reduce the activation energy required for the reaction, so that the reaction can occur under relatively mild conditions.
Subsequently, the reaction temperature and reaction time are strictly regulated. The temperature has a great impact on the reaction rate and product selectivity. According to the characteristics of the reaction, the temperature is maintained within a specific range, so that the reaction can be carried out efficiently without too many side reactions. The reaction time must also be precisely controlled. If it is too short, the reaction will be incomplete, and if it is too long, it may lead to the decomposition of the product or other adverse changes.
After the reaction is completed, use appropriate separation and purification techniques to extract the target product from the reaction mixture. Common separation methods include distillation, extraction, column chromatography, etc. After separation and purification, a pure 1- (2-deoxy-2-fluoro-β-D-arabinofuranosyl) -5-iodouracil product can be obtained.
During the preparation process, it is necessary to follow strict operating procedures and pay attention to the details of each step to ensure the quality and yield of the product. In this way, 1- (2-deoxy-2-fluoro-β-D-arabinofuranosyl) -5-iodouracil can be obtained that meets the requirements.
What are the potential side effects of 1- (2-deoxy-2-fluoro-.beta. -d-arabinofuranosyl) -5-iodouracil?
1 - (2 - deoxy - 2 - fluoro - β - D - arabinofuranosyl) - 5 - iodouracil, although this drug has a therapeutic effect, it also has various potential side effects.
It may cause changes in the blood system, such as a decrease in the number of white blood cells and platelets. Blood cells are like soldiers guarding the body. Reducing the number of blood cells weakens the body's ability to resist evil and is prone to various diseases, causing patients to feel tired and tired, and their ability to resist the invasion of external evil is greatly reduced.
It also affects the digestive system, and nausea, vomiting, and diarrhea are common. The spleen and stomach are the foundation of the day after tomorrow, and the main company transports and transforms the essence of water and valley. The side effects of this drug disturb the transportation and transformation of the spleen and stomach. The reverse stomach qi causes nausea and vomiting, and the intestinal conduction loss is diarrhea, which makes the patient's diet difficult and nutrient intake is also hindered.
In addition, it may damage the function of the liver and kidney. Liver and kidney are like purifiers of the body, responsible for metabolism and excretion of waste. The side effects of the drug involve the liver and kidney, causing their functions to be damaged, and toxins in the body are difficult to excrete in time, or cause toxins to accumulate, causing more serious diseases.
And the drug may affect the nervous system, causing patients to experience dizziness, headache, insomnia, etc. The brain is the palace of the primordial spirit, and the nervous system is disturbed, causing the patient to be uneasy, sleep poorly, and the quality of life also decreases. When taking medication, doctors should carefully observe the patient's reaction and weigh the pros and cons to ensure the safety and effectiveness of medication.