Eicosapentaenoic acid cysteine adduct

Identification

Molecular formula

C₂₃H₃₇NO₅S

CAS number

Not Known

IUPAC name

6-(2-amino-2-carboxy-ethyl)sulfanyl-5-hydroxy-icosa-7,9,11,14-tetraenoic acid

State

At room temperature, the compound is typically a solid. Its state can vary slightly depending on humidity and exact formulation, but it is generally stable as a powder or crystalline solid.

Melting point (Celsius)

66.00

Melting point (Kelvin)

339.20

Boiling point (Celsius)

523.20

Boiling point (Kelvin)

796.40

General information

Molecular weight

421.63g/mol

Molar mass

421.6290g/mol

Density

1.2500g/cm³

Appearence

The compound appears as an off-white to pale yellow solid, depending on its purity and specific structural configuration. It generally appears as a powder when isolated in laboratory settings.

Comment on solubility

Solubility of 6-(2-amino-2-carboxy-ethyl)sulfanyl-5-hydroxy-icosa-7,9,11,14-tetraenoic acid

The solubility of 6-(2-amino-2-carboxy-ethyl)sulfanyl-5-hydroxy-icosa-7,9,11,14-tetraenoic acid (C₂₃H₃₇NO₅S) can vary based on several factors, influenced by its unique molecular structure. Here are some key points regarding its solubility:

Polar vs. Nonpolar: The presence of polar functional groups such as amino (-NH₂) and carboxylic acid (-COOH) moieties suggests that this compound can interact favorably with polar solvents, enhancing its solubility in water.
Hydrogen Bonding: The structure allows for potential hydrogen bonding interactions, primarily due to the -COOH group and hydroxyl (-OH) group, which can significantly increase solubility in aqueous solutions.
Chain Structure: The long hydrocarbon chain may have implications on solubility in nonpolar solvents; thus, while the compound is likely soluble in water, its solubility in organic solvents may be limited.
Concentration Dependence: As with many organic compounds, the solubility can be concentration-dependent, with saturation limits that can change based on temperature and pH of the solution.

In summary, due to the combination of polar functional groups and the hydrocarbon structure, 6-(2-amino-2-carboxy-ethyl)sulfanyl-5-hydroxy-icosa-7,9,11,14-tetraenoic acid is expected to show better solubility in polar solvents like water compared to nonpolar solvents. Understanding these solubility characteristics is crucial for applications in pharmaceuticals and biochemistry.

Interesting facts

Interesting Facts About 6-(2-amino-2-carboxy-ethyl)sulfanyl-5-hydroxy-icosa-7,9,11,14-tetraenoic Acid

6-(2-amino-2-carboxy-ethyl)sulfanyl-5-hydroxy-icosa-7,9,11,14-tetraenoic acid, commonly known as a derivative of eicosapentaenoic acid (EPA), is a fascinating compound with various biological implications. Here are some noteworthy points:

Biochemical Role: This compound is a vital precursor in the biosynthesis of important bioactive lipids that play crucial roles in inflammatory responses and cellular signaling.
Antioxidative Properties: Its antioxidant capabilities help in combating oxidative stress, which is linked to various chronic diseases.
Potential Therapeutic Applications: Research has indicated that it may have potential in therapeutic applications for cardiovascular health, due to its role in lipid metabolism.
Structural Complexity: The structural nature of this molecule showcases significant complexity, which contributes to its unique biochemical properties.
Natural Sources: Compounds like this are often found in marine oils and certain algae, linking them to dietary sources of omega-3 fatty acids.

In summary, 6-(2-amino-2-carboxy-ethyl)sulfanyl-5-hydroxy-icosa-7,9,11,14-tetraenoic acid is more than just a chemical entity; it represents a significant connection between nutrition, health, and biochemical processes. As research continues, we may uncover even more about its potential benefits and applications in medicine.

Synonyms

DTXSID70868376

6-[(2-amino-2-carboxyethyl)sulfanyl]-5-hydroxyicosa-7,9,11,14-tetraenoic acid