CAS 102029-93-6
:Adenosine 5′-(trihydrogen diphosphate), P′→5′-ester with 1-(1,4-dihydro-1-β-D-ribofuranosyl-3-pyridinyl)ethanone, disodium salt
Description:
Adenosine 5′-(trihydrogen diphosphate), P′→5′-ester with 1-(1,4-dihydro-1-β-D-ribofuranosyl-3-pyridinyl)ethanone, disodium salt, commonly referred to by its CAS number 102029-93-6, is a complex chemical compound that combines elements of nucleotide chemistry and organic synthesis. This substance features a nucleotide backbone, specifically adenosine diphosphate (ADP), which is modified by the addition of a pyridine derivative. The presence of the disodium salt form indicates that it is likely soluble in water, which is a characteristic of many nucleotides and their derivatives. The compound may exhibit biological activity, potentially influencing metabolic pathways or serving as a substrate or inhibitor in enzymatic reactions. Its structure suggests it could interact with various biological macromolecules, including proteins and nucleic acids, due to the presence of both phosphate groups and a ribofuranosyl moiety. Overall, this compound represents a unique intersection of biochemistry and pharmacology, with potential applications in research and therapeutic contexts.
Formula:C22H30N6O14P2·2Na
InChI:InChI=1S/C22H30N6O14P2.2Na/c1-10(29)11-3-2-4-27(5-11)21-17(32)15(30)12(40-21)6-38-43(34,35)42-44(36,37)39-7-13-16(31)18(33)22(41-13)28-9-26-14-19(23)24-8-25-20(14)28;;/h2,4-5,8-9,12-13,15-18,21-22,30-33H,3,6-7H2,1H3,(H,34,35)(H,36,37)(H2,23,24,25);;/t12-,13-,15-,16-,17-,18-,21-,22-;;/m1../s1
InChI key:InChIKey=VONVDLUZPBGDIO-MNXWHKAMSA-N
SMILES:O[C@H]1[C@H](N2C=3C(N=C2)=C(N)N=CN3)O[C@H](COP(OP(OC[C@H]4O[C@H]([C@H](O)[C@@H]4O)N5C=C(C(C)=O)CC=C5)(=O)O)(=O)O)[C@H]1O.[Na]
Synonyms:- Adenosine 5′-(trihydrogen diphosphate), P′→5′-ester with 1-(1,4-dihydro-1-β-D-ribofuranosyl-3-pyridinyl)ethanone, disodium salt
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Found 2 products.
3-Acetylpyridine adenine dinucleotide disodium, reduced form
CAS:<p>Reduced synthetic analog of NADH with an acetylpyridine modification. It is used as a reducing substrate to study the mechanisms of NAD(P)+-dependent reductases and to probe the active sites and catalytic processes of these important enzymes through its altered spectroscopic and binding properties. The disodium salt ensures good solubility for biochemical applications.</p>Formula:C22H30N6O14P2•Na2Purity:Min. 95%Color and Shape:Slightly Yellow PowderMolecular weight:710.43 g/mol

