
CAS 1042976-44-2
:N6-Furfuryl-2'-C-methyladenosine
Description:
N6-Furfuryl-2'-C-methyladenosine is a modified nucleoside that features a furfuryl group at the N6 position of the adenine base and a methyl group at the 2' position of the ribose sugar. This compound is of interest in biochemical research due to its potential roles in RNA biology and its implications in the study of gene expression and regulation. The presence of the furfuryl group may influence the stability and binding properties of the nucleoside, potentially affecting its interactions with RNA and proteins. Additionally, the methylation at the 2' position can impact the nucleoside's reactivity and its incorporation into RNA strands. Such modifications are often studied for their effects on the structure and function of RNA, as well as their potential therapeutic applications. The compound is typically characterized by techniques such as NMR spectroscopy, mass spectrometry, and chromatography to confirm its structure and purity. Overall, N6-Furfuryl-2'-C-methyladenosine represents a valuable tool for exploring the complexities of nucleic acid chemistry.
Formula:C16H19N5O5
Synonyms:- Adenosine, N-(2-furanylmethyl)-3'-C-methyl-
- N6-Furfuryl-2'-C-methyladenosine
- N6-(2-furanylmethyl)-9H-(3-C-methyl-β-D-ribofuranosyl)adenine
- N6-Furfuryl-2’-C-methyladenosine
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N6-Furfuryl-2'-C-methyladenosine
CAS:<p>N6-Furfuryl-2'-C-methyladenosine is a Nucleoside Derivative - 6-Modified purine nucleoside; 2'-Modified nucleoside.</p>Formula:C16H19N5O5Color and Shape:SolidMolecular weight:361.35
