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Coenzyme A

Coenzyme A Structure
CAS No.
85-61-0
Chemical Name:
Coenzyme A
Synonyms
COA;COA-SH;COENZYME A HYDRATE;Lucina;Coalip;Aluzime;Thiol-CoA;SHUIRUJIE;COENZYME A;CONENZYME A
CBNumber:
CB8854470
Molecular Formula:
C21H36N7O16P3S
Molecular Weight:
767.53
MOL File:
85-61-0.mol
MSDS File:
SDS
Modify Date:
2024/7/25 20:04:51

Coenzyme A Properties

Density 1.96±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Store in freezer, under -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
Merck 13,2491
BRN 77809
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)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
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
1-10
TSCA  Yes
HS Code  2933299090
NFPA 704
0
1 0

Coenzyme A price More Price(9)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) C4282 Coenzyme A hydrate ≥85% (UV, HPLC) 85-61-0 10MG ₹6040.35 2022-06-14 Buy
Sigma-Aldrich(India) C4282 Coenzyme A hydrate ≥85% (UV, HPLC) 85-61-0 25MG ₹11853.38 2022-06-14 Buy
Sigma-Aldrich(India) C4282 Coenzyme A hydrate ≥85% (UV, HPLC) 85-61-0 100MG ₹22169.6 2022-06-14 Buy
ottokemi C 0513 CoASH (Coenzyme A-SH), 80% 85-61-0 10mg ₹6003 2022-05-26 Buy
ottokemi C 0513 CoASH (Coenzyme A-SH), 80% 85-61-0 25mg ₹10044 2022-05-26 Buy
Product number Packaging Price Buy
C4282 10MG ₹6040.35 Buy
C4282 25MG ₹11853.38 Buy
C4282 100MG ₹22169.6 Buy
C 0513 10mg ₹6003 Buy
C 0513 25mg ₹10044 Buy

Coenzyme A Chemical Properties,Uses,Production

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.

Chemical Properties

yellowish lyophilisate

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: Coenzyme A is a thiol comprising a panthothenate unit in phosphoric anhydride linkage with a 3',5'-adenosine diphosphate unit; and an aminoethanethiol unit. It has a role as an Escherichia coli metabolite, a mouse metabolite and a coenzyme. It is functionally related to an ADP. It is a conjugate acid of a coenzyme A(4-).

General Description

Coenzyme A (CoA) is a cofactor with a molecular weight of 797 Da. Its biological structure is formed from pantothenic acid (vitamin B5), cysteine and adenosine triphosphate through an evolutionarily conserved pathway. CoA is primarily involved in cellular oxidative pathways, including fatty acid beta-oxidation, carbohydrate, amino acid oxidation, and the Krebs cycle; as well as in lipid synthesis, protein modification, and membrane transport. CoA serves as a carrier for the activation of acyl groups, which can be transferred to amides, esters, or acid anhydrides. CoA can also be regulate a variety of metabolic processes at different levels as substrates, allosteric regulators, and through post-translational modifications of histones and other non-histone proteins. It is an essential cofactor in all organisms.

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.]

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Coenzyme A Spectrum

Lucina Thiol-CoA Coenzyme A,75%,free acid, lyophilized Coenzyme A, free acid, hydrate (COA) coenzyme A(4-) COENZYME A [(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 CONENZYME A Coenzyme a, free acid Coenzyme A, free acid, lyophilized, min. 75% (enzym.) COENZYME A FREE ACID FROM YEAST Coenzyme A, free acid, lyophilized, 75% Coenzyme A / Q0 / Q10 COENZYM A FREE ACID COENZYME A (COA) CoenzyMe A hydrate (free acid) Coenzyme A hydrate,CoA [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 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 Aluzime Coenzyme ASH D-Coenzyme A Coalip SHUIRUJIE Coenzyme A, Free Acid(CoA) COENZYMEA 96%, TRILITH. D1GM Coenzyme A USP/EP/BP (((2R,3S,4R,5R)-5-(6-Amino-9H-purin-9-yl)-4-hydroxy-2-(((hydroxy((hydroxy((R)-3-hydroxy-2,2-dimethyl-3-((2-((2-sulfanylethyl)carbamoyl)ethyl)carbamoyl)propoxy)phosphoryl)oxy)phosphoryl)oxy)methyl)oxolan-3-yl)oxy)phosphonic acid Delivery Coenzyme CoASH (Coenzyme A-SH), 80% [[(2S,3R,4S,5S)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl] [(3R)-3-hydroxy-2,2-dimethyl-4-oxo-4-[[3-oxo-3-(2-sulfanylethylamino)propyl]amino]butyl] hydrogen phosphate COENZYME A HYDRATE COA COA-SH Coenzyme A (8CI, 9CI, ACI) Acetyl Coenzyme 85-61-0 85-16-0 C21H36N7O16P3S C21H36N7O16P3S3H2O C21H38N7O17P3S C21H32N7O16P3S C21H36N7O16P3SxH2O C21H36N7O16P3SH2O Metabolic Libraries Lipid Library Nucleosides, Nucleotides, Oligonucleotides Biochemicals and Reagents BioChemical Coenzyme A and Derivatives Metabolomics Vitamin series 85-61-0