| Field | Specification |
|---|---|
| Mfr No | |
| Activity | |
| Alternative Names | Caproyl Coenzyme A sodium salt |
| Coenzyme A Class | |
| Form | Lyophilized powder |
| Molecular Weight | |
| Product Type | |
| Purity | |
| Shipping | |
| SMILES | |
| Solubility | Soluble in water |
| Storage |
Overview
Hexanoyl Coenzyme A, Sodium 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: Caproyl Coenzyme A sodium salt.
Key Elements and Design Rationale
- Formula / MW / Purity: C27H43N7O17P3S · xNa; 865.68 g/mol (free acid basis); ≥ 95%. The Sodium salt form provides enhanced aqueous stability.
- Form / Solubility: Lyophilized powder; Soluble in water.
- Synonyms: Caproyl Coenzyme A sodium salt.
- Origin: Biosynthetic synthesis.
Biological Background
Hexanoyl coenzyme A (hexanoyl-CoA) is a medium-chain fatty acyl-CoA that serves as a preferred substrate for ghrelin O-acyltransferase (GOAT) in enzyme assays, outperforming octanoyl-CoA. GOAT, the enzyme responsible for the acylation of ghrelin, exhibits a higher catalytic efficiency with hexanoyl-CoA, which enhances ghrelin's biological activity in regulating appetite and energy balance. Hexanoyl-CoA acts as a biosynthetic precursor to olivetolic acid, a key intermediate in the production of phytocannabinoids such as cannabigerolic acid (CBGA). This makes hexanoyl-CoA a functionally important molecule in both mammalian metabolism and plant secondary metabolite biosynthesis (Yang et al., 2016; Gagne et al., 2012).
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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