Home > Products > Specialty & Industrial Chemicals > Specialty Chemicals > Acetyl coenzyme A sodium salt
Acetyl coenzyme A sodium salt structure, CAS 102029-73-2

Acetyl coenzyme A sodium salt

CAS Number102029-73-2

SynonymsACETHYL COENZYME A SODIUM SALT; ACETYL COENZYME A (C2:0) SODIUMPREPARED ENZYMATICA; Acetyl-Coenzym A; acetyl coa; C2:0; Acetyl Coenzyme A Trisodium Salt; coenzyme A acetyl derivative (C2:0),sodium salt; Acetyl Coenzyme A; MFCD00078858

Molecular FormulaC23H38N7O17P3S

Molecular Weight875.52

Purity≥93 (HPLC)%

Density1.9±0.1 g/cm3

Boiling Point

Melting Point

Flash Point

Appearancepowder

EINECS

MSDSChineseEnglish

Symboltransportation

Signal WordWarning

Cat. No.: 2A-9049871 Purity: ≥93 (HPLC)%
Change View

Please Login or Create an Account to: See VlP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

Quality Control of [ 102029-73-2 ] Purity: ≥93 (HPLC)% SDS Specification MoL

Chemical & Physical Properties
CAS Number102029-73-2
Catalog No.2A-9049871
Chinese Name乙酰辅酶 A 钠盐
SynonymsACETHYL COENZYME A SODIUM SALT; ACETYL COENZYME A (C2:0) SODIUMPREPARED ENZYMATICA; Acetyl-Coenzym A; acetyl coa; C2:0; Acetyl Coenzyme A Trisodium Salt; coenzyme A acetyl derivative (C2:0),sodium salt; Acetyl Coenzyme A; MFCD00078858
Molecular FormulaC23H38N7O17P3S
Molecular Weight875.52
Purity≥93 (HPLC)
Density1.9±0.1 g/cm3
Appearancepowder
Storage Condition-20 °C
ApplicationAcetyl Coenzyme A trisodium (Acetyl-CoA trisodium) is an important metabolic intermediate. Acetyl Coenzyme A trisodium is the actual molecule of glycolytic pyruvate into the tricarboxylic acid (TCA) c
PubChem ID24890621
MDL NumberMFCD00078858
SMILESO[C@H]1[C@](O[C@@H]([C@H]1OP(O)(O)=O)COP(OP(OCC(C)(C)[C@@H](O)C(NCCC(NCCSC(C)=O)=O)=O)(O)=O)(O)=O)([H])N2C3=NC=NC(N)=C3N=C2.[3Na]
InChI1S/C23H38N7O17P3S.Na/c1-12(31)51-7-6-25-14(32)4-5-26-21(35)18(34)23(2,3)9-44-50(41,42)47-49(39,40)43-8-13-17(46-48(36,37)38)16(33)22(45-13)30-11-29-15-19(24)27-10-28-20(15)30;/h10-11,13,16-18,22,33-34H,4-9H2,1-3H3,(H,25,32)(H,26,35)(H,39,40)(H,41,42)(H2,24,27,28)(H2,36,37,38);/q;+1/p-1/t13-,16-,17-,18?,22-;/m1./s1
InChI KeyHNLIOWFIXSPFEC-WLYMNMRISA-M
NACRES CodeNA.51
UNSPSC41106305
Hazard Symbolstransportation
MSDSmsds/49871_1_102029_73_2.pdf
BioactivityAcetyl Coenzyme A trisodium (Acetyl-CoA trisodium) is a central metabolic intermediate. Acetyl Coenzyme A trisodium is the actual molecule through which glycolytic pyruvate enters the tricarboxylic acid (TCA) cycle, is a key precursor of lipid synthesis, and is the sole donor of the acetyl groups for acetylation. Acetyl Coenzyme A trisodium acts as a potent allosteric activator of pyruvate carboxylase (PC)[1]. Related Catalog Research Areas >> Metabolic Disease In Vitro Acetyl-coenzyme A (Acetyl-CoA) is a membrane-impermeant molecule constituted by an acetyl moiety (CH3CO) linked to coenzyme A (CoA), a derivative of vitamin B5 and cysteine, through a thioester bond. As thioester bonds are energy rich, the chemical structure of acetyl-CoA facilitates the transfer of the acetyl moiety to a variety of acceptor molecules, including amino groups on proteins[1]. In most mammalian cells, Acetyl-coenzyme A (Acetyl-CoA) is predominantly generated in the mitochondrial matrix by various metabolic circuitries, namely glycolysis, β-oxidation, and the catabolism of branched amino acids. Cytosolic Acetyl-coenzyme A is the precursor of multiple anabolic reactions that underlie the synthesis of fatty acids and steroids, as well as specific amino acids including glutamate, proline, and arginine[1]. In Vivo Mice deprived of food (but with access to water ad libitum) for 24 hr exhibit a significant reduction in total Acetyl-coenzyme A (Acetyl-CoA) levels in several organs, including the heart and muscles, corresponding to a decrease in protein acetylation levels. However, the same experimental conditions have no major effects on Acetyl-coenzyme A concentrations in the brain and actually increase hepatic Acetyl-coenzyme A and protein acetylation levels. Ethanol intake augments Acetyl-coenzyme A levels in hepatic mitochondria[1]. References [1]. Federico Pietrocola, et al. Acetyl coenzyme A: a central metabolite and second messenger. Cell Metab. 2015 Jun 2;21(6):805-21. Chemical & Physical Properties Density 1.9±0.1 g/cm3 Molecular Formula C23H38N7O17P3S Molecular Weight 809.571 Exact Mass 809.125793 PSA 418.36000 LogP -3.89 Index of Refraction 1.718 InChIKey CRTIJMBXIFKWCA-JHJDYNLLSA-N SMILES CC(=O)SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP(=O)(O)OP(=O)(O)OCC1OC(n2cnc3c(N)ncnc32)C(O)C1OP(=O)(O)O.[Na+].[Na+].[Na+] Storage condition -20 °C
Use ofAcetyl Coenzyme A trisodium (Acetyl-CoA trisodium) is a central metabolic intermediate. Acetyl Coenzyme A trisodium is the actual molecule through which glycolytic pyruvate enters the tricarboxylic acid (TCA) cycle, is a key precursor of lipid synthesis, and is the sole donor of the acetyl groups for acetylation. Acetyl Coenzyme A trisodium acts as a potent allosteric activator of pyruvate carboxylase (PC)[1]. Properties Name Acetyl coenzyme A sodium salt Synonym More Synonyms Acetyl Coenzyme A trisodium Biological Activity Description Acetyl Coenzyme A trisodium (Acetyl-CoA trisodium) is a central metabolic intermediate. Acetyl Coenzyme A trisodium is the actual molecule through which glycolytic pyruvate enters the tricarboxylic acid (TCA) cycle, is a key precursor of lipid synthesis, and is the sole donor of the acetyl groups for acetylation. Acetyl Coenzyme A trisodium acts as a potent allosteric activator of pyruvate carboxylase (PC)[1]. Related Catalog Research Areas >> Metabolic Disease In Vivo Mice deprived of food (but with access to water ad libitum) for 24 hr exhibit a significant reduction in total Acetyl-coenzyme A (Acetyl-CoA) levels in several organs, including the heart and muscles, corresponding to a decrease in protein acetylation levels. However, the same experimental conditions have no major effects on Acetyl-coenzyme A concentrations in the brain and actually increase hepatic Acetyl-coenzyme A and protein acetylation levels. Ethanol intake augments Acetyl-coenzyme A levels in hepatic mitochondria[1]. References [1]. Federico Pietrocola, et al. Acetyl coenzyme A: a central metabolite and second messenger. Cell Metab. 2015 Jun 2;21(6):805-21. Chemical & Physical Properties Molecular Formula C23H38N7O17P3S Exact Mass 809.125793 PSA 418.36000 LogP -3.89 Index of Refraction 1.718 InChIKey CRTIJMBXIFKWCA-JHJDYNLLSA-N
Transport InfoProduct name: Purity: 90.0%
MSDS Transport InfoModule 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 Names specified by the United Nations (UN) European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Dangerous Regulations: No International Maritime Transport Dangerous Regulations Maritime Pollutants: No International Air Transport Risk Regulations: No 14.6 Special reminder to users No data available
Related Products in Specialty Chemicals
1-(2-Ethoxyethyl)-1,3-dihydro-2H-benzimidazol-2-one101953-61-12A-9049864
Birch-Me101978-01-22A-9049865
Tetrahydrothien-3-ylamine101993-01-52A-9049867
3,6,9,12,15,18,21,24,27-Nonaoxaoctacosanoic acid102013-72-92A-9049868
AMPSO sodium salt102029-60-72A-9049870
N-(3-Sulfopropyl)-3,3',5,5'-tetramethylbenzidine sodium salt102062-36-22A-9049874
Azetidin-3-amine dihydrochloride102065-86-12A-9049875
3-Azetidinamine dihydrochloride102065-89-42A-9049876
Bis(4-biphenylyl)amine102113-98-42A-9049879
1,1,4,4-Tetramethyl-6-nitro-1,2,3,4-tetrahydronaphthalene102121-55-12A-9049881
Browse all Specialty Chemicals products »
Contact Us

Phone:

630-322-8886

630-322-8887

Email:

[email protected]

Office Locations:

Chicago, IL, USA

San Francisco, CA, USA