| Field | Specification |
|---|---|
| Mfr No | |
| Activity | |
| Alternative Names | CoA trilithium salt, CoA Li3 |
| Coenzyme A Class | |
| Form | Lyophilized powder |
| Molecular Weight | |
| Product Type | |
| Purity | |
| Shipping | |
| SMILES | |
| Solubility | Soluble in water |
| Storage |
Overview
Coenzyme A, Trilithium salt is a biochemical supplied by Coenza for use in enzymology and metabolic research. Available as Lyophilized powder, purity ≥ 98%, suitable for in vitro assays and pathway studies.
Also known as: CoA trilithium salt, CoA Li3.
Key Elements and Design Rationale
- Formula / MW / Purity: C21H33N7O16P3S · 3Li; 767.53 g/mol (free acid basis); ≥ 98%. The Trilithium salt form provides enhanced aqueous stability.
- Form / Solubility: Lyophilized powder; Soluble in water.
- Synonyms: CoA trilithium salt, CoA Li3.
- Origin: Biosynthetic synthesis.
Biological Background
Coenzyme A is an essential metabolic cofactor for all living organisms, involved in over 100 metabolic reactions, such as fatty acid metabolism, pyruvate oxidation through the tricarboxylic acid (TCA) cycle, and the production of secondary metabolites. It plays a crucial role in the mechanisms of a wide variety of enzymes. CoA facilitates the removal of lipid peroxides by increasing the mobilization of fatty acids and promotes the repair of plasma membranes by activating phospholipid synthesis (Leonardi et al., 2005; Sibon & Strauss, 2016).ApplicationsCoenzyme A Lithium Salt is widely utilized in biochemical and clinical research due to its involvement in key metabolic pathways and its ability to support cellular functions. It is used to study enzyme activities, particularly those involved in lipid metabolism and cellular detoxification processes. In addition, Coenzyme A Lithium Salt is valuable for investigating mechanisms of membrane repair and stabilization, making it useful in research focused on conditions related to oxidative stress and metabolic disorders (Leonardi et al., 2005; Spry et al., 2008).
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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