ChemicalBook--->CAS DataBase List--->85-61-0

85-61-0

85-61-0 Structure

85-61-0 Structure
IdentificationBack Directory
[Name]

Coenzyme A
[CAS]

85-61-0
[Synonyms]

COA
COA-SH
Coalip
Lucina
Aluzime
Thiol-CoA
COENZYME A
CONENZYME A
Coenzyme ASH
D-Coenzyme A
COENZYME A (COA)
COENZYME A HYDRATE
COENZYM A FREE ACID
Coenzyme A/Q0/Q10
Coenzyme a, free acid
Coenzyme A hydrate,CoA
CoenzyMe A hydrate (free acid)
COENZYME A FREE ACID FROM YEAST
Coenzyme A, free acid, hydrate (COA)
Coenzyme A,75%,free acid, lyophilized
Coenzyme A, free acid, lyophilized, 75%
Coenzyme A, free acid, lyophilized, min. 75% (enzym.)
Adenosine 5'-(trihydrogen diphosphate) 3'-(dihydrogen phosphate) P'-[(R)-3-hydroxy-4-[[3-[(2-mercaptoethyl)amino]-3-oxopropyl]amino]-2,2-dimethyl-4-oxobutyl] ester
[5-(6-Aminopurin-9-yl)-4-hydroxy-2-[[hydroxy-[hydroxy-[3-hydroxy-2,2-dimethyl-3-[2-(2-sulfanylethylcarbamoyl)ethylcarbamoyl]propoxy]phosphoryl]oxy-phosphoryl]oxymethyl]oxolan-3-yl]oxyphosphonic acid
[(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-2-[[hydroxy-[hydroxy-[3-hydroxy-2,2-dimethyl-3-[2-(2-sulfanylethylcarbamoyl)ethylcarbamoyl]propoxy]phosphoryl]oxy-phosphoryl]oxymethyl]oxolan-3-yl]oxyphosphonic acid
[EINECS(EC#)]

201-619-0
[Molecular Formula]

C21H36N7O16P3S
[MDL Number]

MFCD06795839
[MOL File]

85-61-0.mol
[Molecular Weight]

767.54
Chemical PropertiesBack Directory
[Appearance]

yellowish lyophilisate
[density ]

1.96±0.1 g/cm3(Predicted)
[storage temp. ]

−20°C
[solubility ]

PBS (pH 7.2): 10 mg/ml
[form ]

A crystalline solid
[pka]

9.6 (thiol); pK 6.4 (secondary phosphate); pK 4.0 (adenine NH3+)
[color ]

White to light yellow
[biological source]

yeast
[Merck ]

13,2491
[BRN ]

77809
[Cosmetics Ingredients Functions]

SKIN CONDITIONING
[InChIKey]

RGJOEKWQDUBAIZ-IBOSZNHHSA-N
[SMILES]

SCCNC(=O)CCNC(=O)[C@@H](C(COP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C3N=CN=C(N)C=3N=C2)[C@H](O)[C@@H]1OP(=O)(O)O)(C)C)O
[LogP]

-4.358 (est)
[EPA Substance Registry System]

Coenzyme A(85-61-0)
Hazard InformationBack Directory
[Chemical Properties]

yellowish lyophilisate
[Description]

Coenzyme A (CoA) is an essential cofactor functioning as an acyl group carrier and carbonyl-activating group for the citric acid cycle and fatty acid metabolism. About 4% of cellular enzymes utilize CoA as a substrate. It is synthesized from pantothenic acid in a 5-step process that requires ATP. The pantothenate kinase step of the CoA biosynthetic pathway has been identified as a target for the development of antibacterial compounds.
[Uses]

A hydrated form of Coenzyme A (CoA) is a useful biochemical research chemical, used in the preparation of high-yielding cell-free protein synthesis platforms.
[Definition]

ChEBI: Tetraanion of coenzyme A.
[General Description]

Coenzyme A is structurally composed of 2-aminoethanethiol, pantothenic acid and phosphorylated adenosine phosphate.
[Biochem/physiol Actions]

Coenzyme A is a cofactor involved in acyl group transfer. It is essential for carbohydrate, lipid and protein metabolism. Coenzyme A acts as a cofactor for vitamin B coenzymes.
[Purification Methods]

The white powder is best stored in an inert atmosphere in the dark in sealed ampoules after drying in vacuo over P2O5 at 34o. It has UV: max 259 nm ( 16,800) in H2O. [Buyske et al. J Am Chem Soc 76 3575 1954.] It is soluble in H2O but insoluble in EtOH, Et2O and M2CO. It is readily oxidised in air and is best kept as the more stable trilithium salt [Moffat & Khorana J Am Chem Soc 83 663 1961; see also Beinert et al. J Biol Chem 200 384 1953, De Vries et al. J Am Chem Soc 72 4838 1950, Gregory et al. J Am Chem Soc 74 854 1952 and Baddiley Adv Enzymol 16 1 1955]. [Beilstein 26 III/IV 3663.]
[References]

[1] ROBERTA LEONARDI. Coenzyme A: Back in action[J]. Progress in lipid research, 2005, 44 2: Pages 125-153. DOI: 10.1016/j.plipres.2005.04.001
[2] BROWN G M. Biosynthesis of Pantothenic Acid and Coenzyme A[J]. Comprehensive Biochemistry, 1900, 168 1: 0. DOI: 10.1016/b978-0-444-40871-6.50012-x
[3] T. BEGLEY E S C Kinsland. The biosynthesis of coenzyme A in bacteria.[J]. Vitamins and Hormones, 2001, 20 1: 157-171. DOI: 10.1016/s0083-6729(01)61005-7
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H315-H335
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
[Safety Statements ]

24/25
[WGK Germany ]

3
[F ]

1-10
[TSCA ]

Yes
[HS Code ]

2933299090
[Storage Class]

11 - Combustible Solids
Raw materials And Preparation ProductsBack Directory
[Raw materials]

AMBERLITE(R) IRC-50-->Adenine-->Cysteamine-->D-Ribose-->D-Pantothenic acid
[Preparation Products]

2-(3-methylbut-2-enoylamino)acetic acid-->2,5-Piperidinedione-->N-Isovalerylglycine-->Caprylylglycine
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

Coenzyme A(85-61-0).msds
Spectrum DetailBack Directory
[Spectrum Detail]

Coenzyme A(85-61-0)ESR
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