CAS 108347-97-3
:succinyl coenzyme A sodium
Description:
Succinyl coenzyme A sodium, with the CAS number 108347-97-3, is a biochemical compound that plays a crucial role in metabolic pathways, particularly in the citric acid cycle (Krebs cycle) and fatty acid synthesis. It is a derivative of coenzyme A, which is essential for the activation and transport of acyl groups in various biochemical reactions. The sodium salt form enhances its solubility in aqueous solutions, making it more accessible for biological processes. Succinyl CoA is involved in the synthesis of heme and is a key intermediate in the metabolism of certain amino acids. Its structure features a succinyl group linked to coenzyme A, which contains a pantothenic acid moiety, a phosphate group, and an adenosine diphosphate (ADP) component. This compound is typically used in research and clinical settings to study metabolic functions and enzyme activities. Due to its role in energy metabolism, it is also of interest in the context of various metabolic disorders and potential therapeutic applications.
Formula:C25H39N7NaO19P3S
InChI:InChI=1/C25H40N7O19P3S.2Na/c1-25(2,20(38)23(39)28-6-5-14(33)27-7-8-55-16(36)4-3-15(34)35)10-48-54(45,46)51-53(43,44)47-9-13-19(50-52(40,41)42)18(37)24(49-13)32-12-31-17-21(26)29-11-30-22(17)32;;/h11-13,18-20,24,37-38H,3-10H2,1-2H3,(H,27,33)(H,28,39)(H,34,35)(H,43,44)(H,45,46)(H2,26,29,30)(H2,40,41,42);;/q;2*+1/p-2/t13-,18-,19-,20?,24-;;/m1../s1
InChI key:InChIKey=MZSOFLIDFHDGAA-YXKORUMSSA-N
SMILES:O[C@H]1[C@H](N2C=3C(N=C2)=C(N)N=CN3)O[C@H](COP(OP(OCC([C@H](C(NCCC(NCCSC(CCC(O)=O)=O)=O)=O)O)(C)C)(=O)O)(=O)O)[C@H]1OP(=O)(O)O.[Na]
Synonyms:- Coenzyme A, S-(hydrogen butanedioate), sodium salt
- disodium 1-{(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-3-[(hydroxyphosphinato)oxy]tetrahydrofuran-2-yl}-3,5,9-trihydroxy-8,8-dimethyl-10,14,19-trioxo-2,4,6-trioxa-18-thia-11,15-diaza-3,5-diphosphadocosan-22-oate 3,5-dioxide (non-preferred name)
- coenzyme A succinyl derivative, trisodium salt
- SUCCINYL COENZYME A SODIUM SALT
- succinyl coenzyme A sodium
- Succinyl coenzyme A sodium salt >=85%
- Succinyl CoA, Li-salt
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Succinyl-Coenzyme A sodium salt
CAS:Succinyl-Coenzyme A sodium saltFormula:C25H40N7NaO19P3SPurity:≥80%Molecular weight:890.6Succinyl coenzyme A sodium salt
CAS:Formula:C25H40N7O19P3SPurity:≥ 90.0%Color and Shape:White to pale yellow powderMolecular weight:867.61Succinyl-Coenzyme A sodium salt
CAS:Succinyl-Coenzyme A sodium salt(Succinyl-CoA sodium salt) participates in the citric acid cycle, where it is converted to succinic acid.Succinyl-Coenzyme A (Formula:C25H37N7Na3O19P3SPurity:88%Color and Shape:White SolidMolecular weight:933.552Succinyl-Coenzyme A Na salt
CAS:Formula:C25H40N7O19P3S.NaPurity:>95%Color and Shape:SolidMolecular weight:867.61Coenzyme A, S-(hydrogen butanedioate), xsodium salt
CAS:Formula:C25H40N7NaO19P3SPurity:85%Color and Shape:SolidMolecular weight:890.5966530000009Succinyl-Coenzyme A sodium salt (Standard)
CAS:Succinyl-Coenzyme A sodium salt (Standard) is a reference standard for research and analysis in studies involving Succinyl-Coenzyme A sodium salt. Succinyl-Coenzyme A sodium salt(Succinyl-CoA sodium salt) participates in the citric acid cycle, where it is converted to succinic acid.Succinyl-Coenzyme A (sodium salt) is involved in a variety of metabolic reactions in living organisms, and plays an important role in the body.Succinyl-Coenzyme A (sodium salt) is involved in heme synthesis. Succinyl-Coenzyme A (sodium salt) is involved in the synthesis of hemoglobin and is used in the study of metabolic, neurological, and hematological disorders caused by nutritional vitamin B12 deficiency, which results in a deficiency in Succinyl-Coenzyme A synthesis.Formula:C25H37N7Na3O19P3SMolecular weight:933.552Succinyl Coenzyme A Sodium
CAS:Controlled ProductFormula:C25H39N7NaO19P3SColor and Shape:NeatMolecular weight:889.589Succinyl coenzyme A sodium
CAS:Succinyl coenzyme A sodium (SCCA) is a membrane-permeable probe that can be used to measure the mitochondrial membrane potential. SCCA is transported into mitochondria and reduced by dehydrogenase, resulting in an increase in the concentration of its oxidized form, succinic semialdehyde. This increase in extracellular concentrations of succinic semialdehyde can be detected using high performance liquid chromatography with fluorescence detection. The use of this probe has been shown to be useful for measuring mitochondrial function in live cells and tissues, and for investigating genetic disorders that affect mitochondrial function.
Formula:C25H40N7O19P3S•NaxPurity:Min. 95%Molecular weight:889.59 g/mol









