Uridine, 2′-deoxy-5-iodo- is a compound that possesses potential therapeutic properties, particularly in the field of neuroscience. Studies have shown that it may play a role in enhancing cognitive function, mood regulation, and overall brain health. As such, individuals may find relevance in this compound for improving mental performance, memory consolidation, and overall well-being in their everyday lives. Additionally, ongoing research into the impact of Uridine, 2′-deoxy-5-iodo- on neurological disorders such as Alzheimer’s disease further underscores its potential significance in the realm of healthcare and wellness.
Table of Contents:
- 💡 Commercial Applications
- ⚗️ Chemical & Physical Properties
- 🏭 Production & Procurement
- ⚠️ Safety Considerations
- 🔬 Potential Research Directions
- 🧪 Related Compounds
💡 Commercial Applications
Uridine, 2′-deoxy-5-iodo-, is a nucleoside analog that has various commercial and industrial applications. It is often used in the synthesis of nucleotide probes for studying DNA and RNA interactions. Additionally, it is utilized in the production of radioactive tracers for studying cellular processes.
In the field of drug and medication development, Uridine, 2′-deoxy-5-iodo-, has potential applications as an antiviral agent. It has shown promising results in inhibiting the replication of certain viruses, making it a candidate for further research in the development of antiviral drugs. Furthermore, its ability to modulate neurotransmitter levels in the brain suggests potential applications in treating neurological conditions.
Overall, Uridine, 2′-deoxy-5-iodo-, has a range of commercial, industrial, and pharmaceutical applications. Its unique properties make it a valuable tool for studying nucleic acid interactions, as well as a potential candidate for the development of antiviral medications and treatments for neurological disorders. Further research and development in these areas may lead to groundbreaking advances in science and medicine.
⚗️ Chemical & Physical Properties
Uridine, 2′-deoxy-5-iodo-, appears as a white crystalline powder with no distinct odor. It is a solid compound at room temperature and is commonly used in biochemical research.
The molar mass of Uridine, 2′-deoxy-5-iodo-, is approximately 368.05 g/mol with a density of 2.32 g/cm³. Compared to common food items, such as sugar (molar mass of 342.3 g/mol) and salt (density of 2.16 g/cm³), Uridine falls within similar ranges.
Uridine, 2′-deoxy-5-iodo-, has a melting point of around 232-235°C and a boiling point of approximately 534-536°C. These values differ significantly from those of common food items like butter (melting point of 32-35°C) and water (boiling point of 100°C).
Uridine, 2′-deoxy-5-iodo-, is sparingly soluble in water and does not exhibit significant viscosity. This contrasts with common food items like sugar and salt, which are highly soluble in water and may exhibit varying degrees of viscosity when dissolved.
🏭 Production & Procurement
Uridine, 2′-deoxy-5-iodo- is produced through a multi-step chemical synthesis process in a laboratory setting. The starting materials for this production include various chemicals that undergo reactions to yield the final compound. This compound is typically purified and isolated through chromatographic techniques before being used for research purposes.
Uridine, 2′-deoxy-5-iodo- can be procured from specialized chemical suppliers that produce and distribute research-grade compounds. Researchers can place orders for this compound through these suppliers, who typically provide it in various quantities to meet the specific needs of the customer. Once procured, the compound is typically packaged in appropriate containers and shipped using standard shipping methods to ensure its safe transport.
The transportation of Uridine, 2′-deoxy-5-iodo- from the supplier to the research facility is usually carried out using standard shipping practices for chemical compounds. This may involve using specialized packaging materials and carriers to ensure the safety and integrity of the compound during transit. Upon arrival at the research facility, the compound is typically stored according to specific guidelines to maintain its stability and quality for future use in experiments.
⚠️ Safety Considerations
Safety considerations for Uridine, 2′-deoxy-5-iodo- should be taken seriously due to its potential hazards. This compound can be harmful if swallowed, inhaled, or if it comes into direct contact with the skin or eyes. It may cause irritation or allergic reactions in some individuals. As such, appropriate precautionary measures should be implemented when handling Uridine, 2′-deoxy-5-iodo- to minimize the risk of exposure.
Hazard statements for Uridine, 2′-deoxy-5-iodo- include: Harmful if swallowed. Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation. May cause an allergic skin reaction. These hazard statements underscore the importance of handling Uridine, 2′-deoxy-5-iodo- with caution and implementing appropriate safety measures to prevent adverse health effects.
Precautionary statements for Uridine, 2′-deoxy-5-iodo- include: Avoid breathing dust/fume/gas/mist/vapors/spray. Wear protective gloves/protective clothing/eye protection/face protection. IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water/shower. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. These precautionary statements emphasize the importance of following safety protocols to minimize the risk of exposure and ensure safe handling of Uridine, 2′-deoxy-5-iodo-.
🔬 Potential Research Directions
One potential research direction of Uridine, 2′-deoxy-5-iodo- could involve elucidating its pharmacological properties and potential therapeutic applications. Studies may focus on investigating its role in nucleic acid synthesis, as well as its interactions with cellular targets and molecular pathways.
Another avenue of research could explore the pharmacokinetics and metabolism of Uridine, 2′-deoxy-5-iodo- to better understand its absorption, distribution, and excretion in the body. This could provide valuable insights into its bioavailability and potential for sustained drug delivery.
Furthermore, research efforts may be directed towards exploring the effects of Uridine, 2′-deoxy-5-iodo- on various disease states, such as cancer, viral infections, and neurological disorders. Investigating its mechanisms of action and potential synergies with other drugs could lead to the development of novel therapeutic strategies.
🧪 Related Compounds
One similar compound to Uridine, 2′-deoxy-5-iodo- is 2′-deoxyuridine, which is a nucleoside composed of 2′-deoxyribose and uracil. This compound differs from Uridine by lacking the hydroxyl group at the 2′ position on the sugar moiety. The presence of the iodine atom at the 5′ position in Uridine, 2′-deoxy-5-iodo- enhances its usefulness in radiolabeling applications.
Another compound similar to Uridine, 2′-deoxy-5-iodo- is 2′-deoxy-5-azauridine, which is a derivative of uridine with an azido group in place of the iodine atom at the 5′ position. This modification alters the chemical properties of the compound, making it useful in bioconjugation and chemical crosslinking experiments. Despite this difference, 2′-deoxy-5-azauridine shares structural similarities with Uridine, 2′-deoxy-5-iodo-.
A third compound with similarities to Uridine, 2′-deoxy-5-iodo- is 2′-deoxy-5-fluorouridine, which contains a fluorine atom in place of the iodine at the 5′ position. This compound is often used as a substrate in enzyme kinetics studies due to its structural resemblance to Uridine, 2′-deoxy-5-iodo-. The presence of the fluorine atom alters the physicochemical properties of the compound, influencing its biological activity.