What is the chemical structure of 2- ({3- (acetylamino) -5- [acetyl (methyl) amino] -2,4,6-triiodobenzoyl} amino) -2-deoxy-alpha-d-glycero-hexopyranose?

This is the chemical structure analysis of 2 - {3 - (acetamido) - 5 - [acetyl (methyl) amino] - 2,4,6 - triiodobenzoyl} amino - 2 - deoxy - α - D - glycerol - hexopyranose. The structure of this compound is quite complex, let me explain it in detail.

First, its main body is the structure of a 2 - deoxy - α - D - glycerol - hexopyranose, and this sugar ring structure is the basis. In the second position of the sugar ring, there is a complex side chain connected. This side chain starts from an amino group, which is in turn connected to a benzoyl group.

The benzoyl group is further explored. In the third position of the benzene ring, there is an acetamide substitution; in the fifth position, there is an acetyl (methyl) amino substitution; and in the 2,4,6 positions of the benzene ring, there is an iodine atom substitution. The presence of these substituents endows the compound with unique chemical and physical properties.

In this structure, the sugar ring part has the characteristics of a carbohydrate, while the benzoyl group and its substituents introduce changes in aromaticity, polarity and reactivity. Acetamide and the acyl group in acetyl (methyl) amino can participate in hydrogen bonding and affect the interaction between molecules. The benzene ring substituted by triiodide has a significant impact on the stability, solubility and biological activity of the compound due to the heavy atom effect of the iodine atom.

In conclusion, the chemical structure of 2 - {3 - (acetamido) - 5 - [acetyl (methyl) amino] - 2,4,6 -triiodobenzoyl} amino - 2 - deoxy - α - D - glycerol - hexopyranose is the result of the ingenious combination of various structural units, and the interaction of each part determines its behavior in the fields of chemistry and biology.

What are the main uses of 2- ({3- (acetylamino) -5- [acetyl (methyl) amino] -2,4,6-triiodobenzoyl} amino) -2-deoxy-alpha-d-glycero-hexopyranose?

2-%28+%7B3-%28acetylamino%29-5-%5Bacetyl%28methyl%29amino%5D-2%2C4%2C6-triiodobenzoyl%7Damino%29-2-deoxy-alpha-d-glycero-hexopyranose is a rather complex organic compound. This compound has important uses in the field of medicine, especially in contrast agents.

Guanfu contrast agent is used in medical imaging examinations, which can make the structure and organs of the body more clearly visible in the image. The iodine atoms contained in 2-%28+%7B3-%28acetylamino%29-5-%5Bacetyl%28methyl%29amino%5D-2%2C4%2C6-triiodobenzoyl%7Damino%29-2-deoxy-alpha-d-glycero-hexopyranose have strong absorption capacity for X-rays due to their high atomic number. In X-ray imaging, computed tomography (CT) and other examinations, after the contrast agent containing this compound is injected into the human body, it will accumulate in specific organs or tissues, thereby changing the local absorption characteristics of X-rays. In this way, when imaging, the target area can be clearly distinguished from the surrounding tissue, helping physicians to more accurately diagnose diseases such as tumors and vascular diseases.

Furthermore, the specific chemical structure of this compound makes it biocompatible. It can exist relatively stably in the body and will not have serious adverse effects on normal physiological functions of the human body, reducing the occurrence of adverse reactions such as allergic reactions, and providing protection for the safety of angiography.

In summary, 2-%28+%7B3-%28acetylamino%29-5-%5Bacetyl%28methyl%29amino%5D-2%2C4%2C6-triiodobenzoyl%7Damino%29-2-deoxy-alpha-d-glycero-hexopyranose plays a key role in the field of medical imaging diagnosis with its unique structure and properties, and contributes greatly to the early detection and accurate diagnosis of diseases.

What is the safety of 2- ({3- (acetylamino) -5- [acetyl (methyl) amino] -2,4,6-triiodobenzoyl} amino) -2-deoxy-alpha-d-glycero-hexopyranose?

2-%28+%7B3-%28acetylamino%29-5-%5Bacetyl%28methyl%29amino%5D-2%2C4%2C6-triiodobenzoyl%7Damino%29-2-deoxy-alpha-d-glycero-hexopyranose, this is a complex organic compound. Its safety needs to be scrutinized from many aspects.

Look at its chemical structure, containing groups such as acetamido, acetyl methylamino and triiodobenzoylamino. There are many iodine atoms, which may affect the stability and reactivity of the compound. In organisms, the existence of iodine may cause special physiological effects, or involve metabolism, toxicity, etc.

From the theory of toxicology, there is no relevant experimental data to determine its exact toxicity. However, organic compounds containing iodine may have potential toxicity, or stimulate tissues and interfere with physiological processes. If it enters the human body, or interacts with biological macromolecules such as proteins and nucleic acids, it will damage cell function, and even cause cancer, teratogenicity, and mutation.

In terms of environmental safety, its degradation and fate in the environment are also important. Complex structures may make it difficult to degrade, accumulate in the environment, endanger the ecosystem. Or pass through the food chain and have long-term effects on higher organisms.

In summary, in order to clarify the safety of 2-%28+%7B3-%28acetylamino%29-5-%5Bacetyl%28methyl%29amino%5D-2%2C4%2C6-triiodobenzoyl%7Damino%29-2-deoxy-alpha-d-glycero-hexopyranose, it is necessary to conduct in-depth toxicological experiments and environmental behavior studies to accurately evaluate its potential impact on human health and the environment.

What is the market outlook for 2- ({3- (acetylamino) -5- [acetyl (methyl) amino] -2,4,6-triiodobenzoyl} amino) -2-deoxy-alpha-d-glycero-hexopyranose?

2-%28+%7B3-%28acetylamino%29-5-%5Bacetyl%28methyl%29amino%5D-2%2C4%2C6-triiodobenzoyl%7Damino%29-2-deoxy-alpha-d-glycero-hexopyranose, this is a complex organic compound. Its market prospects are quite promising.

In the field of medicine, it has potential medicinal value. Because the structure contains many special groups, it may act on specific biological targets. For example, the iodine atoms contained in it may give the compound certain imaging properties, which can be used in the development of contrast agents. With precise imaging, doctors can clearly understand the visceral organs and lesions of the body, which is of great significance for disease diagnosis.

Furthermore, in the field of organic synthesis, the compound may become an important intermediate. Its complex structure can be chemically modified to derive a variety of new compounds, paving the way for the development of new drugs and materials science. Organic chemists can use this to explore novel synthetic pathways, expand the structural diversity of compounds, and promote the progress of organic synthetic chemistry.

However, there are also challenges. Its complex structure makes it difficult to synthesize, and the production cost may be high. And the metabolic process, safety and side effects in living organisms need to be studied in depth. Only by overcoming all these problems can this compound bloom in the market and make outstanding contributions to human health and scientific progress.

What are the production processes for 2- ({3- (acetylamino) -5- [acetyl (methyl) amino] -2,4,6-triiodobenzoyl} amino) -2-deoxy-alpha-d-glycero-hexopyranose?

To prepare 2 - {3 - (acetamido) -5 - [acetyl (methyl) amino] -2, 4, 6 - triiodobenzoyl} amino - 2 - deoxygenated - α - D - glycerol - hexopyranose, the production process is as follows:

The starting material needs to be prepared with benzene ring and sugar structure related raw materials. The first step is to iodize the benzene ring, select suitable iodizing reagents such as iodine elemental substance and appropriate catalyst, and successfully introduce iodine atoms at the 2,4,6 positions of the benzene ring at a specific temperature and reaction time. The key to this step is to precisely control the reaction conditions and prevent excessive or insufficient iodization.

Next, an amino-related group is added to the iodine-containing benzene ring. Acylation reaction is used to acylate with acetyl chloride and other acylating reagents. Under the catalysis of a suitable base, acetamide is introduced at the 3rd position of the benzene ring, and acetyl (methyl) amino is connected at the 5th position. This process requires strict reaction solvent, temperature and reactant ratio to ensure reaction selectivity.

Sugar structure part, select a suitable 2-deoxy - α - D-glycerol-hexopyranose derivative, and activate the sugar terminal hydroxyl group, often treated with halogenated reagents to make it more reactive.

Then, the modified benzene ring is connected to the sugar structure by means of condensation reaction. The condensation agent such as carbodiimide can promote the condensation of the two in a suitable reaction system to form the target product.

After the reaction is completed, a series of separation and purification methods, such as column chromatography, recrystallization, etc., remove impurities, and obtain high purity 2 - {3 - (acetamido) -5 - [acetyl (methyl) amino] -2,4,6 - triiodobenzoyl} amino - 2 - deoxygenated - α - D - glycerol - hexopyranose. Rigorous testing is required after each step of the reaction. TLC, nuclear magnetic resonance and other technologies are used to ensure that the reaction achieves the expected effect and the product structure is correct.