| Field | Specification |
|---|---|
| Mfr No | |
| Activity | |
| Alternative Names | Coenzyme A, CoA, CoA-SH, Aluzime, Coalip, Thiol-CoA |
| Coenzyme A Class | |
| Form | Lyophilized powder |
| Molecular Weight | |
| Product Type | |
| Purity | |
| Shipping | |
| SMILES | |
| Solubility | Soluble in water |
| Storage |
Overview
Coenzyme A, Free Acid 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: Coenzyme A, CoA, CoA-SH, Aluzime, Coalip, Thiol-CoA.
Key Elements and Design Rationale
- Formula / MW / Purity: C21H36N7O16P3S; 767.53 g/mol; ≥ 95%. The Free Acid form provides enhanced aqueous stability.
- Form / Solubility: Lyophilized powder; Soluble in water.
- Synonyms: Coenzyme A, CoA, CoA-SH, Aluzime, Coalip, Thiol-CoA.
- Origin: Biosynthetic synthesis.
Biological Background
Coenzyme A (CoA) is a universal metabolic cofactor synthesized from cysteine, pantothenate, and ATP. It is notable for its role in the synthesis and oxidation of fatty acids and the oxidation of pyruvate in the citric acid cycle (Leonardi et al., 2005). All genomes sequenced to date encode enzymes that use coenzyme A as a substrate, and around 4% of cellular enzymes use it, or a thioester form of it, as a substrate (Sibon & Strauss, 2016).ApplicationsCoenzyme A (CoA) Free Acid is widely used in biochemical research and drug development due to its role as a cofactor in numerous enzymatic reactions, particularly in acyl group transfer processes. It is extensively applied in studies of metabolic pathways, such as the citric acid cycle and fatty acid metabolism, to explore enzyme functions, regulatory mechanisms, and potential therapeutic targets (Leonardi et al., 2005). CoA Free Acid is also valuable in drug discovery for evaluating inhibitors or activators of CoA-dependent enzymes, which are crucial for developing treatments for metabolic disorders and infections (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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