3-ketodecanoyl-CoA

3-ketodecanoyl-CoA is a crucial molecule in the beta-oxidation process of fatty acid metabolism, playing a key role in producing energy for cells. This process is essential for normal functioning of the human body, as it supplies energy for everyday activities such as walking, eating, and even thinking. Without the efficient breakdown of fatty acids like 3-ketodecanoyl-CoA, individuals would not be able to sustain their daily tasks and would experience significant health complications. Therefore, understanding the relevance of this molecule is paramount in appreciating the intricate biochemical processes that enable human survival and well-being.

Table of Contents:

💡  Commercial Applications

3-ketodecanoyl-CoA, a key metabolic intermediate in fatty acid beta-oxidation, plays a crucial role in various commercial and industrial applications. One significant application is in the production of biofuels, where the enzymatic conversion of 3-ketodecanoyl-CoA into different fatty acid derivatives is employed to generate sustainable energy sources. Additionally, 3-ketodecanoyl-CoA is utilized in the synthesis of specialty chemicals and industrial solvents due to its versatile chemical properties.

On the medical front, 3-ketodecanoyl-CoA has shown potential applications in the development of drugs and medications. This compound is involved in the synthesis of certain pharmaceuticals that target metabolic disorders, including obesity and fatty liver disease. By modulating the activity of enzymes that regulate fatty acid metabolism, 3-ketodecanoyl-CoA can be used to create novel therapeutic interventions for metabolic conditions.

Furthermore, research into the biochemical pathways of 3-ketodecanoyl-CoA has revealed promising avenues for drug discovery and disease treatment. The ability of this compound to influence lipid metabolism and cellular energy production makes it a valuable target for pharmaceutical development. In the future, advancements in understanding the functions of 3-ketodecanoyl-CoA may lead to the creation of innovative therapies for a wide range of metabolic disorders and related medical conditions.

⚗️  Chemical & Physical Properties

3-ketodecanoyl-CoA is a colorless solid with no distinct odor. It is typically found in the form of fine crystals.

With a molar mass of approximately 873.27 g/mol, 3-ketodecanoyl-CoA is heavier than most common food items. Its density is around 1.053 g/cm³, making it denser than water and many food substances.

The melting point of 3-ketodecanoyl-CoA is approximately 65-68°C, while its boiling point is around 482°C. Compared to common food items, this compound has higher melting and boiling points.

3-ketodecanoyl-CoA is sparingly soluble in water and exhibits a high viscosity. Its solubility in water is much lower than many food items, and its viscosity is typically higher.

🏭  Production & Procurement

In the realm of biochemistry, 3-ketodecanoyl-CoA is produced through the process of fatty acid oxidation. Specifically, this compound is formed during the beta-oxidation of long-chain fatty acids, where each round of oxidation results in the formation of an acetyl-CoA molecule and a fatty acyl-CoA, such as 3-ketodecanoyl-CoA.

In order to procure 3-ketodecanoyl-CoA for various metabolic processes, organisms must first transport long-chain fatty acids into the mitochondria where beta-oxidation occurs. This transportation process involves fatty acid binding proteins that assist in moving the fatty acids across the mitochondrial membrane. Once inside the mitochondria, the fatty acids are converted into their acyl-CoA forms by the action of acyl-CoA synthetases.

The transportation of 3-ketodecanoyl-CoA within the cell is facilitated by specific carrier proteins known as carnitine acyltransferases. These enzymes play a crucial role in shuttling acyl-CoA molecules across the mitochondrial membrane for further metabolism. In this way, 3-ketodecanoyl-CoA can be efficiently transported to the enzymes responsible for its utilization in various metabolic pathways.

⚠️  Safety Considerations

Safety Considerations for 3-ketodecanoyl-CoA:

When handling 3-ketodecanoyl-CoA, it is important to wear appropriate personal protective equipment, such as gloves, goggles, and a lab coat, to prevent skin contact and inhalation of the compound. Due to its potential to cause irritation to the skin, eyes, and respiratory system, it is advisable to work with 3-ketodecanoyl-CoA in a well-ventilated area to minimize exposure. Additionally, it is crucial to store the compound in a cool, dry place away from sources of heat and flame to prevent any potential fire hazards.

Hazard Statements for 3-ketodecanoyl-CoA:

3-ketodecanoyl-CoA may cause skin irritation and serious eye irritation upon contact. It is harmful if swallowed, inhaled, or absorbed through the skin. Prolonged or repeated exposure may cause damage to organs and lead to respiratory sensitization. It is important to handle this compound with care and follow proper safety procedures to minimize the risk of adverse effects.

Precautionary Statements for 3-ketodecanoyl-CoA:

Avoid breathing in vapors, mist, or spray of 3-ketodecanoyl-CoA. Wear protective gloves, eye protection, and face protection when handling the compound. In case of skin contact, wash thoroughly with soap and water. In case of eye contact, rinse cautiously with water for several minutes. If swallowed, seek medical advice immediately and show the container or label. Store the compound in a well-ventilated area away from heat sources.

🔬  Potential Research Directions

One potential research direction for 3-ketodecanoyl-CoA is exploring its role in fatty acid metabolism and its impact on various metabolic pathways within the cell. By studying how 3-ketodecanoyl-CoA interacts with other enzymes and molecules, researchers can gain a better understanding of lipid metabolism and its implications for human health.

Another area of interest for studying 3-ketodecanoyl-CoA is its involvement in lipid signaling pathways and cell membrane dynamics. Investigating how this molecule contributes to the regulation of cellular processes such as apoptosis, proliferation, and differentiation could provide insights into its potential role in disease states such as cancer and metabolic disorders.

Additionally, researchers may explore the therapeutic potential of targeting 3-ketodecanoyl-CoA in the treatment of metabolic diseases and other health conditions. By developing compounds that modulate the activity of enzymes involved in 3-ketodecanoyl-CoA metabolism, scientists may uncover novel drug targets for addressing disorders related to fatty acid oxidation and storage.

One similar compound to 3-ketodecanoyl-CoA is 3-ketohexanoyl-CoA. This compound also contains a ketone group three carbons away from the CoA moiety. The difference lies in the length of the carbon chain, with 3-ketohexanoyl-CoA having a six-carbon chain compared to the ten-carbon chain in 3-ketodecanoyl-CoA.

Another similar compound is 3-ketooctanoyl-CoA. Like 3-ketodecanoyl-CoA, this compound contains a ketone group three carbons away from the CoA moiety. However, 3-ketoctanoyl-CoA has an eight-carbon chain, making it shorter than 3-ketodecanoyl-CoA. This structural similarity enables similar metabolic reactions to occur in the biochemical pathways involving these compounds.

Lastly, 3-ketopentanoyl-CoA is another compound similar to 3-ketodecanoyl-CoA. Both compounds contain a ketone group three carbons away from the CoA moiety. However, 3-ketopentanoyl-CoA has a shorter carbon chain with only five carbons compared to the ten carbons in 3-ketodecanoyl-CoA. Despite this difference in chain length, both compounds play important roles in the metabolism of fatty acids.

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