
CAS 1921-48-8
:thionicotinamide adenine dinucleotide,*reduced fo
Description:
Thionicotinamide adenine dinucleotide (reduced form), commonly abbreviated as TADH, is a coenzyme involved in various biochemical reactions, particularly in redox processes. It is a derivative of nicotinamide adenine dinucleotide (NADH) and plays a crucial role in cellular metabolism, serving as an electron carrier in oxidation-reduction reactions. The reduced form indicates that it has accepted electrons, making it essential for energy production in cellular respiration. TADH is characterized by its ability to participate in enzymatic reactions, facilitating the transfer of electrons and protons. This coenzyme is also involved in the synthesis of nucleotides and the regulation of metabolic pathways. Its structure includes a nicotinamide moiety, an adenine unit, and a phosphate group, contributing to its biochemical functionality. The CAS number 1921-48-8 uniquely identifies this compound in chemical databases, aiding in its recognition and study in various scientific research contexts. Overall, TADH is significant in biochemistry for its role in energy metabolism and cellular function.
Formula:C21H27N7Na2O13P2S
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Found 3 products.
Thionicotinamide Adenine Dinucleotide Disodium Salt reduced form [for Biochemical Research]
CAS:Formula:C21H27N7Na2O13P2SPurity:>93.0%(HPLC)Color and Shape:White to Yellow to Orange powder to crystalMolecular weight:725.47β-Thionicotinamide adenine dinucleotide, reduced form disodium salt
CAS:<p>β-Thionicotinamide adenine dinucleotide, reduced form disodium salt</p>Formula:C21H29N7O13SP2Purity:92%Color and Shape:SolidMolecular weight:725.47g/molThionicotinamide Adenine Dinucleotide Disodium Salt Reduced (Thio-NADH) extrapure, 93%
CAS:Formula:C21H27N7O13SP2Na2Purity:min. 93%Color and Shape:Yellow, PowderMolecular weight:725.47


