Bilirubin
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FSH
UTI
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Aprotinin
Asparaginase
Beta Glucanase
Bromelain
Chymotrypsin
Kallikrein
Lysozyme
Pancreatin
Papain
Pepsin
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Trypsin
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Coenzyme A
Coenzyme A Trilithium
Coenzyme Q10
Beta Glucans
Chitosan
Chondroitin Sulfate
Dextran
Dextran Sulfate Sodium
Glucosamine HCl
Heparin Sodium
Heparinoid
Hyaluronic Acid
Rosemary Extract
Sodium Cholate
Bilirubin
Cytochrome C
Gastric Mucin
HCG
FSH
UTI
PMSG
Aprotinin
Asparaginase
Beta Glucanase
Bromelain
Chymotrypsin
Kallikrein
Lysozyme
Pancreatin
Papain
Pepsin
Streptokinase
Trypsin
Urokinase
Coenzyme A
Coenzyme A Trilithium
Coenzyme Q10
Beta Glucans
Chitosan
Chondroitin Sulfate
Dextran
Dextran Sulfate Sodium
Glucosamine HCl
Heparin Sodium
Heparinoid
Hyaluronic Acid
Rosemary Extract
Sodium Cholate
Jiagen Biotechnologies
Coenzymes

Coenzyme A Trilithium Salt

CAS No:18439-24-2
EINECS No:205-745-7
Synonyms:Coenzyme A trilithium salt from yeast, CoA-Li, Co A-Li, Co A-SH, CoA trilithium salt, Trilithium Coenzyme A, Trilithium salt of CoA

Product Summary

Coenzyme A trilithium salt is a highly soluble, bioactive lithium salt form of Coenzyme A (CoA), a vital cofactor in numerous metabolic and enzymatic processes. This purified form is especially favored in biochemical research, enzymology, and pharmaceutical applications due to its enhanced stability and compatibility with aqueous systems.

  • Formula: C21H33N7O16P3S · 3Li
  • Formula Molecular Weight: 785.33 (as anhydrous trilithium salt)
  • Source: Yeast
  • Lithium content: 1.5% - 4.5%
  • Water: Not more than 8%
  • Purity: Not less than 90%

Function

Coenzyme A trilithium salt acts as a central acyl group carrier in metabolism. It facilitates the formation of thioester bonds with organic acids, converting them into activated acyl-CoA derivatives such as acetyl-CoA, succinyl-CoA, and malonyl-CoA. These intermediates are essential in:
  • The citric acid (TCA) cycle
  • Fatty acid synthesis and oxidation
  • Amino acid metabolism
  • Ketone body production
  • Cholesterol biosynthesis

Mechanism of Action

At the molecular level, CoA features a reactive thiol group (-SH) at its terminus that forms high-energy thioester bonds with acyl groups. This activated form acts as a substrate or cofactor for many enzymes, driving acyl-transfer reactions crucial to cellular metabolism.

The trilithium salt form ensures:

  • Enhanced solubility in aqueous buffers
  • Stability under standard storage and assay conditions
  • Compatibility with enzyme assays and cell-based studies

Applications in Scientific Research

  • Used to study CoA-dependent enzymes like acetyl-CoA synthetase, pyruvate dehydrogenase, and fatty acid synthase.
  • Essential in in vitro reconstitution of metabolic pathways.
  • Investigated in studies of protein CoAlation as a novel oxidative stress response.
  • Screening CoA analogs as enzyme inhibitors or metabolic modulators.
  • Applied in synthetic biology and enzyme-driven transformations.
  • Research into energy metabolism and mitochondrial function.
  • CoA derivatives used in assays to monitor enzyme activity and metabolic flux.

Packaging & Storage

  • Available as white or slightly yellow lyophilized powder
  • Store at -20°C in tightly sealed containers, protected from moisture and light

Jiagen Biotechnologies supplies quality Coenzyme A Trilithium Salt of various specifications.
Contact us at sales@jiagen.ca to place an order.

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