| Field | Specification |
|---|---|
| Activity | |
| Alternative Names | Acetyl-S-CoA Li3, Acetyl-CoA 3Li |
| Coenzyme A Class | |
| Form | Lyophilized powder |
| Molecular Weight | |
| Product Type | |
| Purity | |
| Shipping | |
| SMILES | |
| Solubility | Soluble in water |
| Storage |
Overview
Acetyl Coenzyme A, Lithium salt is a biochemical supplied by Coenza for use in enzymology and metabolic research. Available as Lyophilized powder, purity ≥ 95%, suitable for in vitro assays and pathway studies.
Also known as: Acetyl-S-CoA Li3, Acetyl-CoA 3Li.
Key Elements and Design Rationale
- Formula / MW / Purity: C23H35N7O17P3S · xLi; 809.57 g/mol (free acid basis); ≥ 95%. The Lithium salt form provides enhanced aqueous stability.
- Form / Solubility: Lyophilized powder; Soluble in water.
- Synonyms: Acetyl-S-CoA Li3, Acetyl-CoA 3Li.
- Origin: Synthetic synthesis.
Biological Background
Acetyl Coenzyme A (Acetyl-CoA) is a central molecule in cellular metabolism, playing a pivotal role in energy production and biosynthesis. It is generated by the acetylation of Coenzyme A (CoA) through key enzymatic processes, including pyruvate decarboxylation by pyruvate dehydrogenase, fatty acid ?-oxidation, and the catabolism of certain amino acids. Acetyl-CoA's reactive acetyl group enables its participation in various biochemical pathways, such as the tricarboxylic acid (TCA) cycle, fatty acid synthesis, and cholesterol metabolism, making it essential for cellular energy and biosynthetic processes (Pietrocola et al., 2015; Shi & Tu, 2015).ApplicationsAcetyl Coenzyme A, Lithium Salt, is a key reagent used in metabolic research to study enzymatic functions and metabolic pathways involving acetylation. It is utilized in in vitro studies to explore the TCA cycle, where Acetyl-CoA serves as a critical substrate for citrate formation, and in the biosynthesis of fatty acids and cholesterol. It is also essential for examining acetyl-CoA's role in epigenetic regulation, such as histone acetylation, which affects gene expression and cellular differentiation (Pietrocola et al., 2015; Si
Research Relevance and Current Trends
- Acyl-CoA metabolism increasingly linked to histone acylation marks and epigenetic regulation in cancer and metabolic disease research.
- Growing interest in short-chain fatty acid CoA thioesters as mediators of gut microbiome–host metabolic crosstalk.
- CoA-dependent enzymes investigated as drug targets in infectious disease and neurometabolic disorder research.
Common Research Applications
- Enzyme kinetics assays — direct substrate for acyltransferases, thiolases, and dehydrogenases.
- Metabolic flux analysis — isotope-labeled variants available for stable-isotope tracing.
- In vitro pathway reconstitution for fatty acid β-oxidation, TCA cycle, or polyketide biosynthesis.
- Biochemical characterization of CoA-binding proteins by activity assays or binding measurements.
Notes for Experimental Interpretation
- CoA thioesters hydrolyze at neutral–alkaline pH; prepare working solutions fresh and keep on ice.
- Different salt forms share the same core structure — normalize concentrations using the free-acid MW when comparing across forms.
- Thiol oxidation may occur upon air exposure; use under inert atmosphere or with reducing agents where appropriate.
Need this compound in a format that drops straight into your assay? We can tailor formulation, chemistry, and documentation so your results stay consistent across runs and re-orders.
- Format options: solid or pre-dissolved solution (choose solvent), target concentration, aliquots, light/moisture-protected packaging
- Chemistry options: free base/acid vs salt forms, hydrate/solvate preference, stereoisomer control (single enantiomer or racemate), close analogs
- Add-on labels & handles: D/¹³C/¹⁵N isotopes (LC-MS/internal standards), azide/alkyne or other functional handles for conjugation
- QC & documentation: standard COA or enhanced analytical pack (HPLC/LC-MS/NMR), chiral purity, residual solvents, water content (KF), method-specific specs
- Scale & continuity: mg to gram scale, bulk pricing, lot reservation, repeat-order continuity
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Pietrocola, F., Galluzzi, L., Bravo-San Pedro, J. M., Madeo, F., & Kroemer, G. (2015). Acetyl coenzyme A: A central metabolite and second messenger. Cell Metabolism, 21(6), 805-821.
Shi, L., & Tu, B. P. (2015). Acetyl-CoA and the regulation of metabolism: Mechanisms and consequences. Current Opinion in Cell Biology, 33, 125-131.
Sibon, O. C. M., & Strauss, E. (2016). Coenzyme A: To make it or uptake it? Nature Reviews Molecular Cell Biology, 17(10), 606-607.
Spry, C., Kirk, K., & Saliba, K. J. (2008). Coenzyme A biosynthesis: An antimicrobial drug target. FEMS Microbiology Reviews, 32(1), 56-106.
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