2,6-dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid - 4-amino-1H-imidazole-5-carboxamide (1:1)

The compound formed by the two is the product of the combination of 2,6-dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid and 4-amino-1H-imidazole-5-formamide in a 1:1 ratio.
2,6-dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid, whose structure contains a pyrimidine ring. The 2nd and 6th positions on the pyrimidine ring are carbonyl groups, the 1st, 2nd, 3rd, and 6th positions are saturated bonds, and the 4th position is carboxyl. This structure plays an important role in many biosynthetic pathways, such as pyrimidine nucleotide biosynthesis, which is a key intermediate and participates in the construction of pyrimidine nucleotide skeleton.
4-amino-1H-imidazole-5-formamide, with imidazole ring, hydrogen at 1 position, amino at 4 position, and formamide at 5 position. This substance is significant in the purine nucleotide remedial synthesis pathway and can be converted into purine nucleotides through a series of reactions.
When the two are combined 1:1, or interact through hydrogen bonds, ionic bonds, van der Waals forces, etc., to form a complex. The structure of this complex may change the chemical environment of the original group due to the interaction of the two substances. It may have unique physiological activities in organisms, or affect related metabolic pathways, enzyme activities, etc., and play a role in physiological processes such as cell metabolism and signal transduction. However, more experimental studies are needed to determine its detailed structure and biological activity.

The composition of 2% 2C6-dioxo-1% 2C2% 2C3% 2C6-tetrahydropyrimidine-4-carboxylic acid and 4-amino-1H-imidazole-5-formamide (1:1) has a wide range of uses. In the field of medicine, it may help to create new drugs. Due to their unique structure, after being combined in a specific ratio, they may have unique biological activities. They can act on specific targets in the human body and are expected to be used to treat diseases such as tumors and inflammation. For example, in the treatment of tumors, they may be able to inhibit the proliferation of cancer cells by affecting the metabolic pathways of cancer cells and adding a weapon to the cancer problem.
In biochemical research, this compound (1:1) is also very useful. It can be used as a biochemical reagent to explore specific metabolic processes and signal transduction pathways in organisms. Because its structure is similar to some key substances in organisms, it can simulate or interfere with normal biochemical reactions, helping researchers understand the essence of life activities, and then paving the way for the development of life science.
Furthermore, in the field of materials science, it may also emerge. Appropriate modification and processing may endow materials with unique properties, such as improving material stability, biocompatibility, etc. In terms of biomedical materials, implant materials can better blend with human tissue, reduce immune rejection, and provide a new direction for medical material innovation. Overall, its uses span multiple fields and have broad prospects, making it worth exploring and exploring in depth.

2% 2C6 - dioxo - 1% 2C2% 2C3% 2C6 - tetrahydropyrimidine - 4 - carboxylic acid (2,6 - dioxo - 1,2,3,6 - tetrahydropyrimidine - 4 - carboxylic acid) and 4 - amino - 1H - imidazole - 5 - carboxamide (4 - amino - 1H - imidazole - 5 - formamide) formed in 1:1 substance, its physical properties have the following aspects:
The appearance of this compound or a crystalline powder, often due to the arrangement and interaction of atoms in the molecular structure, it has a specific crystal shape and color. In terms of solubility, since 2,6-dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid contains carboxyl groups and has a certain polarity, 4-amino-1H-imidazole-5-formamide contains amino and amide groups, and also has polarity, so the 1:1 complex may have a certain solubility in polar solvents such as water, but due to the overall size and structural complexity of the molecule, the solubility may be limited; in common organic solvents such as ethanol and acetone, the solubility may vary due to differences in the interaction force between the solvent and the solute.
Its melting point is also affected by intermolecular forces, such as intermolecular hydrogen bonds, van der Waals forces, etc., which make the molecule need specific energy to overcome the binding to achieve phase transition, thus determining the melting point. Due to multiple cyclic structures and polar groups in the structure, the intermolecular interactions are complex, and the melting point may be high.
In addition, the density of the substance is determined by the molecular mass and the degree of molecular packing compactness. The complex molecular structure makes the molecular packing mode unique, which in turn affects the density. In terms of stability, the stability of intramolecular chemical bonds interacts with the external environment, and the pyrimidine ring and imidazole ring are relatively stable in the structure, but functional groups such as carboxyl, amino, and amide groups may participate in chemical reactions. Under extreme conditions such as strong acids, strong bases, and high temperatures, or reactions such as hydrolysis and amide bond fracture occur, the stability decreases.

To prepare the compound of 2% 2C6-dioxo-1% 2C2% 2C3% 2C6-tetrahydropyrimidine-4-carboxylic acid and 4-amino-1H-imidazole-5-formamide (1:1), the following methods can be used.
First, a chemical synthesis method can be used. First, 2% 2C6-dioxo-1% 2C2% 2C3% 2C6-tetrahydropyrimidine-4-carboxylic acid is prepared from a specific starting material through multi-step reaction. Choose the appropriate reaction path, such as starting with a compound containing a specific functional group, through substitution, cyclization and other reactions, according to the reaction conditions, to obtain a pure 2% 2C6-dioxo-1% 2C2% 2C3% 2C6-tetrahydropyrimidine-4-carboxylic acid. At the same time, 4-amino-1H-imidazole-5-formamide is prepared in similar steps. Then, the two are reacted in the presence of suitable solvents, temperatures and catalysts, and combined in a ratio of 1:1 to obtain the target product. After the reaction is completed, the pure product is obtained by separation and purification methods, such as crystallization, column chromatography, etc.
Second, biosynthesis can be used. Find a microorganism or enzyme system with specific enzyme activity, which can catalyze the synthesis of the two substances and promote their binding in a 1:1 ratio. By means of genetic engineering, optimize the expression of microorganisms or enzymes and improve the synthesis efficiency. Construct a suitable reaction system, control the reaction conditions, such as temperature, pH value, etc., so that the biosynthesis can proceed smoothly. After synthesis, the target product can be obtained through appropriate biological separation technology.
Third, the method of solid-phase synthesis can be explored. Fix one of the reactants on the solid-phase carrier, and then react with the other reactant. This can effectively simplify the reaction post-treatment steps and improve the purity of the product. After the reaction, the product was cut off from the solid-phase carrier and purified to obtain a pure compound of 2% 2C6-dioxo-1% 2C2% 2C3% 2C6-tetrahydropyrimidine-4-carboxylic acid and 4-amino-1H-imidazole-5-formamide (1:1).

The substances of Fu 2,6-dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid and 4-amino-1H-imidazole-5-formamide (1:1) are related to safety risks and need to be investigated in detail.
The characteristics of the combination of the two are unknown. In chemical substances, reaction conditions, purity impurities, etc., can cause changes in safety risks. If the reaction is not complete during the preparation process, the residual reactants or by-products may be toxic or irritating, endangering the operator. If the operation site is poorly ventilated, the gas will escape, and inhalation can hurt the lungs and damage health.
In addition, its stability is also important. If this compound is unstable, it may decompose or react in case of heat, light, moisture or other chemicals, causing unpredictable emergencies, generating harmful gases, or reacting violently, causing the risk of fire and explosion.
In terms of storage, improper storage is dangerous. If it is mixed with other things, or reacts due to incompatibility. Uncomfortable temperature and humidity also affect its stability.
In addition, the application scenario also affects safety. For medicine, it is related to patient safety; for industry, it affects production safety and the environment.
Although the exact properties and data of this compound are not known in detail, according to chemical common sense, safety risks may be difficult to ignore. When operating and using, it is necessary to exercise caution, study the characteristics in detail, and follow the specifications to ensure safety.