N-HEPTADECANOYL COENZYME A LITHIUM SALT
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Category | Acyl CoA - Unsaturated Fatty Acid |
Catalog NO. | BPG-3081 |
Product Name | N-HEPTADECANOYL COENZYME A LITHIUM SALT |
CAS | 3546-17-6 |
Molecular Formula | C38H67LiN7O17P3S |
Molecular Weight | 1025.9 |
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Description | Heptadecanoyl-CoA is a long-chain fatty acyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of heptadecanoic acid, It has a role as a metabolite. It is a long-chain fatty acyl-CoA and an 11,12-saturated fatty acyl-CoA. It is functionally related to a heptadecanoic acid. It is a conjugate acid of a heptadecanoyl-CoA(4-). |
Synonyms | heptadecanoyl Coenzyme A (ammonium salt) |
IUPAC Name | S-[2-[3-[[(2R)-4-[[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-2-hydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethyl] heptadecanethioate |
Canonical SMILES | CCCCCCCCCCCCCCCCC(=O)SCCNC(=O)CCNC(=O)C(C(C)(C)COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)N2C=NC3=C(N=CN=C32)N)O)OP(=O)(O)O)O |
InChI | InChI=1S/C38H68N7O17P3S/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-29(47)66-22-21-40-28(46)19-20-41-36(50)33(49)38(2,3)24-59-65(56,57)62-64(54,55)58-23-27-32(61-63(51,52)53)31(48)37(60-27)45-26-44-30-34(39)42-25-43-35(30)45/h25-27,31-33,37,48-49H,4-24H2,1-3H3,(H,40,46)(H,41,50)(H,54,55)(H,56,57)(H2,39,42,43)(H2,51,52,53)/t27-,31-,32-,33+,37-/m1/s1 |
InChIKey | DRABUZIHHACUPI-DUPKZGIXSA-N |
Purity | >99% |
Density | 1.53g/cm3 |
Appearance | Powder |
Shelf Life | 1 Year |
Storage | -20°C |
Exact Mass | 1071.061 |
Hygroscopic | No |
Light Sensitive | No |
Percent Composition | C 42.61%, H 7.25%, N 13.08%, O 25.39%, P 8.68%, S 2.99% |
N-Heptadecanoyl Coenzyme A Lithium Salt is a specialized biochemical reagent used in a variety of research and biotechnological applications. Here are some key applications of N-Heptadecanoyl Coenzyme A Lithium Salt: Lipid Metabolism Studies: N-Heptadecanoyl Coenzyme A Lithium Salt is used to study lipid metabolism by investigating the role of fatty acyl-CoA in various biochemical pathways. Researchers can employ this compound to trace the synthesis and degradation of lipids within cells. This provides insights into basic lipid biochemistry and the regulation of metabolic diseases. Enzyme Activity Assays: This compound is instrumental in studying the activity of enzymes involved in fatty acid metabolism, such as acyl-CoA synthetases and acyl-CoA oxidases. By acting as a substrate or inhibitor in enzyme assays, N-Heptadecanoyl Coenzyme A Lithium Salt helps elucidate enzyme kinetics and mechanisms of action. These studies are vital for understanding metabolic regulation and potential therapeutic targets for metabolic disorders. Membrane Protein Studies: N-Heptadecanoyl Coenzyme A Lithium Salt is also used to explore the interaction of acyl-CoAs with membrane-associated proteins. Researchers can investigate how fatty acyl-CoAs influence the structure and function of membrane proteins, including transporters and receptors. This knowledge contributes to our understanding of cellular membrane dynamics and lipid-protein interactions. Drug Development: In pharmacological research, N-Heptadecanoyl Coenzyme A Lithium Salt is utilized to screen for potential drug compounds that can modulate fatty acid metabolism. By using this reagent in high-throughput assays, scientists can identify inhibitors or activators of key metabolic enzymes. This approach helps in the discovery of new treatments for metabolic diseases such as obesity and type 2 diabetes. |
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