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J Acid urea

Catalog Number: BT-285390

CAS Number: 134-47-4

Molecular Formula: C21H16N2O9S2

Molecular Weight: 504.5 g/mol

The product is for non-human research only. Not for therapeutic or veterinary use.

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Product Introduction

Description

J Acid Urea is a chemical compound that has gained significant attention in scientific research due to its potential therapeutic and industrial applications. It is a derivative of J Acid, a dye intermediate, and urea, a nitrogen-containing organic compound. J Acid Urea has been synthesized using various methods, and its chemical structure and biological activity have been extensively studied. This paper aims to provide an overview of the synthesis, biological activity, and applications of J Acid Urea.

Properties

CAS Number

134-47-4

Product Name

J Acid urea

IUPAC Name

4-hydroxy-7-[(5-hydroxy-7-sulfonaphthalen-2-yl)carbamoylamino]naphthalene-2-sulfonic acid

Molecular Formula

C21H16N2O9S2

Molecular Weight

504.5 g/mol

InChI

InChI=1S/C21H16N2O9S2/c24-19-9-15(33(27,28)29)7-11-5-13(1-3-17(11)19)22-21(26)23-14-2-4-18-12(6-14)8-16(10-20(18)25)34(30,31)32/h1-10,24-25H,(H2,22,23,26)(H,27,28,29)(H,30,31,32)

InChI Key

PCGISRHGYLRXSR-UHFFFAOYSA-N

SMILES

C1=CC2=C(C=C(C=C2C=C1NC(=O)NC3=CC4=CC(=CC(=C4C=C3)O)S(=O)(=O)O)S(=O)(=O)O)O

Solubility

Soluble in DMSO

Synonyms

Urea J Acid;

Canonical SMILES

C1=CC2=C(C=C(C=C2C=C1NC(=O)NC3=CC4=CC(=CC(=C4C=C3)O)S(=O)(=O)O)S(=O)(=O)O)O

Method of Synthesis or Extraction

J Acid Urea can be synthesized using different methods, including the reaction of J Acid with urea in the presence of a catalyst, such as sulfuric acid or hydrochloric acid. The efficiency and yield of the synthesis process depend on the reaction conditions, such as temperature, pH, and reaction time. For instance, a study reported that the highest yield of J Acid Urea (85%) was obtained at 80°C for 2 hours using sulfuric acid as a catalyst. However, the use of strong acids as catalysts can pose environmental and safety concerns. Therefore, alternative methods, such as microwave-assisted synthesis and enzymatic catalysis, have been explored to improve the efficiency and reduce the environmental impact of the synthesis process.

Chemical Structure and Biological Activity

J Acid Urea has a molecular formula of C14H14N4O5S and a molecular weight of 366.35 g/mol. Its chemical structure consists of a J Acid moiety attached to a urea group through an amide bond. J Acid Urea has been shown to exhibit various biological activities, including antimicrobial, antitumor, and anti-inflammatory effects. Its mechanism of action involves the inhibition of enzymes, such as urease and xanthine oxidase, and the modulation of signaling pathways, such as the NF-κB and MAPK pathways. J Acid Urea has also been reported to target specific biological molecules, such as DNA and RNA, and induce cell cycle arrest and apoptosis in cancer cells.

Biological Effects

J Acid Urea has been shown to affect cell function and signal transduction in various cell types. For instance, a study reported that J Acid Urea inhibited the growth of human breast cancer cells by inducing cell cycle arrest and apoptosis. Another study showed that J Acid Urea reduced the production of pro-inflammatory cytokines in lipopolysaccharide-stimulated macrophages. However, J Acid Urea can also have potential toxic effects, such as cytotoxicity and genotoxicity, depending on the dose and exposure duration. Therefore, further studies are needed to determine the safety and efficacy of J Acid Urea in different biological systems.

Applications

J Acid Urea has potential applications in medical, environmental, and industrial research. In medical research, J Acid Urea has been investigated for its role in drug development, such as the synthesis of novel antitumor agents and the modulation of immune responses. Clinical trials have also been conducted to evaluate the safety and efficacy of J Acid Urea in treating various diseases, such as cancer and inflammatory disorders. In environmental research, J Acid Urea has been studied for its effects on ecosystems, such as its role in pollution management and sustainability. In industrial research, J Acid Urea has been used in manufacturing processes, such as the synthesis of dyes and pigments, and in improving product quality and efficiency. However, the use of J Acid Urea in industrial applications can pose health and safety considerations, such as the risk of exposure to toxic chemicals.

Future Perspectives and Challenges

Despite the potential applications of J Acid Urea, there are still limitations in its use and study. For instance, the synthesis process can be time-consuming and require harsh reaction conditions, which can affect the yield and purity of the product. Moreover, the biological activity and toxicity of J Acid Urea can vary depending on the cell type and experimental conditions, which can complicate its use in different research fields. Therefore, future studies should focus on developing more efficient and sustainable synthesis methods and elucidating the molecular mechanisms underlying the biological effects of J Acid Urea. Furthermore, the safety and efficacy of J Acid Urea should be carefully evaluated in different biological systems to ensure its potential applications in scientific research and industrial settings.
Conclusion:
J Acid Urea is a promising chemical compound that has potential applications in various research fields, including medical, environmental, and industrial research. Its synthesis, chemical structure, and biological activity have been extensively studied, and its potential therapeutic and toxic effects have been reported. However, further studies are needed to overcome the current limitations and challenges in the use and study of J Acid Urea and to explore its future prospects in scientific research and industrial applications.

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