CAS 108392-03-6
:Adenosine 5′-(trihydrogen diphosphate), 3′-(dihydrogen phosphate), P′→5′-ester with 3-(aminocarbonyl)-1-α-D-ribofuranosylpyridinium, inner salt, sodium salt
Description:
Adenosine 5′-(trihydrogen diphosphate), 3′-(dihydrogen phosphate), P′→5′-ester with 3-(aminocarbonyl)-1-α-D-ribofuranosylpyridinium, inner salt, sodium salt, is a complex chemical compound characterized by its structure as a nucleotide derivative. It features a ribofuranosyl moiety linked to a pyridinium group, which contributes to its solubility and potential biological activity. The presence of multiple phosphate groups indicates its role in energy transfer and signaling within biological systems. This compound is likely to exhibit high polarity due to the phosphate groups, making it soluble in aqueous environments. Its inner salt formation suggests that it can exist in a zwitterionic state, which may influence its interaction with biological macromolecules. The sodium salt form enhances its stability and solubility, facilitating its use in biochemical applications. Overall, this compound is of interest in biochemical research, particularly in studies related to nucleotide metabolism and cellular signaling pathways.
Formula:C21H28N7O17P3·xNa
InChI:InChI=1S/C21H28N7O17P3.Na/c22-17-12-19(25-7-24-17)28(8-26-12)21-15(31)16(44-46(33,34)35)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)14(30)20(42-10)27-3-1-2-9(4-27)18(23)32;/h1-4,7-8,10-11,13-16,20-21,29-31H,5-6H2,(H7-,22,23,24,25,32,33,34,35,36,37,38,39);/t10-,11-,13-,14-,15-,16-,20+,21-;/m1./s1
InChI key:InChIKey=BWHZOLRRNZGBAU-VUWULMATSA-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)[N+]=5C=C(C(N)=O)C=CC5)(=O)[O-])(=O)O)[C@H]1OP(=O)(O)O.[Na]
Synonyms:- Adenosine 5′-(trihydrogen diphosphate), 3′-(dihydrogen phosphate), P′→5′-ester with 3-(aminocarbonyl)-1-α-D-ribofuranosylpyridinium, inner salt, sodium salt
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Found 1 products.
a-Nicotinamide adenine dinucleotide phosphate
CAS:<p>a-Nicotinamide adenine dinucleotide phosphate (NADP) is a modified form of the natural coenzyme nicotinamide adenine dinucleotide (NAD) and is an important component in cellular metabolism. NADP is also an anticancer agent that inhibits the synthesis of DNA, RNA, and protein. It is used for the treatment of viral infections such as cytomegalovirus (CMV), herpes simplex virus (HSV), varicella zoster virus (VZV), and Epstein-Barr virus (EBV). NADP is also a novel antiviral agent that has been shown to inhibit the enzyme diphosphate kinase, which prevents the production of ATP. This inhibition leads to cell death by disrupting normal energy production. NADP has been shown to be effective against CMV isolates resistant to ganciclovir or foscarnet due to its ability to inhibit DNA synthesis.</p>Formula:C21H28N7O17P3Purity:Min. 95%Molecular weight:743.41 g/mol
