ChemicalBook--->CAS DataBase List--->55672-92-9

55672-92-9

55672-92-9 Structure

55672-92-9 Structure
IdentificationBack Directory
[Name]

COENZYME A SODIUM SALT
[CAS]

55672-92-9
[Synonyms]

COA NA2
Coenzyme A (sodium)
COENZYME A SODIUM SALT
COENZYME A DISODIUM SALT
COENZYME A TRISODIUM SALT
cofactor for acyl transfer
coenzyme A sodium from yeast
Coenzyme A, sodium salt (1:?)
COENZYME A SODIUM SALT HYDRATE
CoenzymeA hydrate sodium salt
COENZYME A, SODIUM CELL CULTURE TESTED
Coenzyme A sodium salt hydrate cofactor for acyl transfer
Coenzyme A Sodium Salt Hydrate (CoA Na2) for molecular biology, 85%
[EINECS(EC#)]

259-747-8
[Molecular Formula]

C21H35N7NaO16P3S
[MDL Number]

MFCD00079020
[MOL File]

55672-92-9.mol
[Molecular Weight]

789.52
Chemical PropertiesBack Directory
[storage temp. ]

−20°C
[solubility ]

H2O: soluble50mg/mL, clear, colorless to faintly yellow
Safety DataBack Directory
[Safety Statements ]

22-24/25
[WGK Germany ]

3
[F ]

3-10-23
Hazard InformationBack Directory
[Uses]

Coenzyme A is suitable for use in:
  • gylcerolipid biosynthesis in porcine adipose tissue
  • an assay to measure the level of Alpha-methylacyl-CoA racemase (AMACR) in human blood samples using a nanoparticle electrochemical biosensor
  • chloramphenicol acetyltransferase (CAT) assay
  • the synthesis of palmitoyl-CoA, which is required for palmitoylation and activation of proteins for regulated membrane fusion
[General Description]

Coenzyme A (CoA) is an essential cofactor in living systems and is synthesized from pantothenic acid (vitamin B5), The CoA levels in mitochondria and peroxisomes correspond to 2-5 mM and 0.7 mM, respectively. Cytosolic CoA is in the range of 0.05 mM to 0.14 mM
[Biochem/physiol Actions]

Coenzyme A (CoA, CoASH, HSCoA) is a coenzyme that facilitates enzymatic acyl-group transfer reactions and supports the synthesis and oxidation of fatty acids. CoA is involved in the mechanisms of a wide variety of enzymes. In the presence of CoASH, organic carboxylic acids form acyl-CoA thioesters, which facilitates enzyme recognition. The acyl-CoA formed from xenobiotic carboxylic acids can add to the compound′s toxicity, which can lead to cellular metabolic dysfunction. It is involved in the oxidation of pyruvate in the Kreb′s cycle. CoA is needed for metabolic events. The bacterial CoA pathway is targeted for antimicrobial development. It mediates acyl group transfer and carbonyl activation. The CoA and its thioester levels are crucial for cellular homeostasis. CoA is also involved in regulating platelet aggregation and vasoconstriction. It acts as an essential cofactor in enzymatic acetyl transfer reactions.
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