Acetyl Coenzyme A, Lithium salt

SKU:BHB21200005
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Coenza
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    Overview
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    Acetyl Coenzyme A, Lithium salt (Lithium salt) is a coenzyme A thioester derivative (C23H35N7O17P3S · xLi; MW 809.57 g/mol (free acid basis)) supplied as Lyophilized powder, purity ≥ 95%, water-soluble. Used as an enzyme substrate/cofactor in metabolic research, enzyme kinetics, and in vitro reconstitution of CoA-dependent pathways.
    Purity ≥ 95%
    Form Lyophilized powder
    Molecular Weight 809.57 g/mol (free acid basis)
    Solubility Soluble in water
    Source Synthetic
    Activity Enzyme Substrate / Cofactor
    Available Options

    Available Sizes:

    • 10 mg
    • 25 mg
    • 50 mg
    • 100 mg

    Shipping: Ambient temperature (styrofoam + ice gels) — shipped on ice packs at ambient temperature (styrofoam + ice gels). Store at −20 °C upon receipt.

    Options selector
    Catalog no. Size
    A-08-Li-10MG 10 mg
    A-08-Li-25MG 25 mg
    A-08-Li-50MG 50 mg
    A-08-Li-100MG 100 mg
    Field Specification
    Activity
    • Enzyme Substrate / Cofactor
    Alternative Names Acetyl-S-CoA Li3, Acetyl-CoA 3Li
    Coenzyme A Class Short-chain
    Form Lyophilized powder
    Molecular Weight 809.57 g/mol (free acid basis)
    Product Type
    • Biochemicals
    • Small Molecules
    Purity ≥ 95%
    Shipping Ambient temperature (styrofoam + ice gels)
    SMILES O=C(CCNC(C(C(C)(COP([O-])(OP([O-])(OCC(C(C1O)OP(O)([O-])=O)OC1N(C2=NC=N3)C=NC2=C3N)=O)=O)C)O)=O)NCCSC(C)=O.[Li+]
    Solubility Soluble in water
    Storage -20°C

    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.
    What is Acetyl Coenzyme A, Lithium salt and what is it used for?
    Acetyl Coenzyme A, Lithium salt is a coenzyme A thioester derivative (MW 809.57 g/mol (free acid basis), C23H35N7O17P3S · xLi) supplied as Lyophilized powder, purity ≥ 95%. The Lithium salt form offers improved aqueous stability compared with some alternatives. It is used as an enzyme substrate and cofactor in metabolic research, enzyme kinetics, and in vitro reconstitution of CoA-dependent biosynthetic and catabolic pathways.
    What are the key physicochemical properties?
    Molecular formula: C23H35N7O17P3S · xLi; MW: 809.57 g/mol (free acid basis); purity: ≥ 95%; form: Lyophilized powder; solubility: Soluble in water; stability: ≥ 2 years. The reactive thioester bond is susceptible to hydrolysis — prepare working solutions fresh and keep on ice during experiments.
    How should Acetyl Coenzyme A, Lithium salt be dissolved for biochemical assays?
    This product is Soluble in water. Dissolve in the appropriate aqueous buffer at the required pH immediately before use. For stock solutions, aliquot into single-use volumes, snap-freeze in liquid nitrogen, and store at −20 °C. Avoid repeated freeze-thaw cycles to prevent hydrolysis.
    What enzymes or metabolic pathways is this compound most relevant to?
    Depending on the acyl chain length and structure, CoA thioester derivatives serve as substrates for acyl-CoA synthetases, acyltransferases, thiolases, acyl-CoA dehydrogenases, carboxylases, and mutases. Relevant pathways include fatty acid β-oxidation, TCA cycle, amino acid catabolism, and polyketide or terpenoid biosynthesis. Refer to the General Information section and the cited literature for compound-specific enzyme associations.
    Does the salt form matter for experimental design?
    The salt form (Free Acid, Lithium, Sodium, Trilithium, Trisodium) shares the same core acyl-CoA structure. Counterions are typically inert at standard assay concentrations. When preparing solutions, use the free-acid MW (809.57 g/mol (free acid basis)) to normalize molar concentrations across salt forms. Verify buffer compatibility if high ionic strength is a concern.

    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

    To quote quickly, tell us: compound name + CAS/structure (SMILES or mol file), intended assay context, solvent preference, salt/stereochemistry requirements, purity/QC level, and the amount (mg–g).

    Can’t find the compound you’re looking for?
    Send the CAS or structure and your specs. We can help source it, suggest close equivalents, or discuss custom synthesis with the right QC documentation (RUO).

    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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