7593-47-7

Basic information

• Product Name: 1H-Imidazole-4-carboximidamide,5-amino-N-hydroxy-
• Synonyms: 1H-Imidazole-4-carboximidamide,5-amino-N-hydroxy-;1H-Imidazole-4-carboximidamide,5-amino-N-hydroxy-(9CI)
• CAS NO: 7593-47-7
• Molecular Formula: C4H7N5O
• Molecular Weight: 141.13128
• Product Categories: VARIOUSAMINE
• Mol File: 7593-47-7.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 514.5±60.0 °C(Predicted)
• Appearance: /
• Density: 1.92±0.1 g/cm3(Predicted)
• PKA: 6.66±0.69(Predicted)
• CAS DataBase Reference: 1H-Imidazole-4-carboximidamide,5-amino-N-hydroxy-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Imidazole-4-carboximidamide,5-amino-N-hydroxy-(7593-47-7)
• EPA Substance Registry System: 1H-Imidazole-4-carboximidamide,5-amino-N-hydroxy-(7593-47-7)

Safety Data

• Hazardous Substances Data: 7593-47-7(Hazardous Substances Data)

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.
2. Heterocyclic compound

Explanation

A heterocyclic compound is a cyclic compound that contains atoms of at least two different elements, in this case, carbon, nitrogen, and oxygen.
3. Imidazole ring

Explanation

Imidazole is a five-membered ring with two nitrogen atoms and three carbon atoms. It is a common structural motif in many biologically active compounds.
4. Carboximidamide group

Explanation

A carboximidamide group is a functional group consisting of a carbonyl group (C=O) attached to an amide group (-CONH-).
5. Amino group

Explanation

An amino group is a functional group with the formula -NH2, which is a basic and nucleophilic group.
6. Potent inhibitor of histone deacetylases

Explanation

Histone deacetylases are enzymes that remove acetyl groups from an ε-N-acetyl lysine amino acid on a histone. Inhibition of these enzymes can lead to altered gene expression and chromatin remodeling.
7. Therapeutic applications in cancer treatment

Explanation

The compound's ability to inhibit histone deacetylases may have potential in the treatment of cancer by modulating gene expression and affecting cell growth and differentiation.
8. Treatment of neurodegenerative diseases

Explanation

Abnormal histone deacetylase activity has been implicated in neurodegenerative diseases. The compound's inhibitory effect on these enzymes may help in the development of treatments for such conditions.
9. Antimicrobial and antifungal properties

Explanation

The compound has been investigated for its ability to inhibit the growth of microorganisms, including bacteria and fungi, which could make it useful in the development of new drugs to combat infectious diseases.
10. Development of new drugs

Explanation

The compound's various biological activities, such as histone deacetylase inhibition, antimicrobial, and antifungal properties, make it a promising candidate for further research and development into new therapeutic agents.

Upstream product

• 5098-11-3 5-amino-1H-imidazole-4-carbonitrile 

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