CAS 85421-89-2
:2-amino-9-(6-deoxyhexofuranosyl)-3,9-dihydro-6H-purin-6-one
Description:
2-amino-9-(6-deoxyhexofuranosyl)-3,9-dihydro-6H-purin-6-one, with the CAS number 85421-89-2, is a purine derivative that exhibits characteristics typical of nucleobases. This compound features a purine ring structure, which is essential in the formation of nucleotides and nucleic acids. The presence of an amino group at the 2-position and a deoxyhexofuranosyl moiety contributes to its biological relevance, particularly in the context of nucleoside analogs. Its structural configuration allows for potential interactions with nucleic acid components, influencing its role in biochemical pathways. The compound is likely to be soluble in polar solvents, reflecting the hydrophilic nature of its functional groups. Additionally, it may exhibit biological activity, potentially acting as an antiviral or anticancer agent, similar to other purine analogs. Overall, this compound's unique structure and functional groups position it as a significant molecule in medicinal chemistry and biochemistry.
Formula:C11H15N5O5
InChI:InChI=1/C11H15N5O5/c1-3(17)7-5(18)6(19)10(21-7)16-2-13-4-8(16)14-11(12)15-9(4)20/h2-3,5-7,10,17-19H,1H3,(H3,12,14,15,20)
SMILES:CC(C1C(C(C(n2cnc3c2[nH]c(=N)nc3O)O1)O)O)O
Synonyms:- 2-(2-Amino-6-hydroxy-purin-9-yl)-5-(1-hydroxy-ethyl)-tetrahydro-furan-3,4-diol
- 5'(R)-C-Methylguanosine
- 6H-Purin-6-one, 2-amino-9-(6-deoxy-β-D-allofuranosyl)-1,9-dihydro-
- 5’(R)-C-Methylguanosine
- 9-(6'-deoxy-beta-D-allofuranosyl)guanine
- See more synonyms
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Found 2 products.
5'(R)-C-Methylguanosine
CAS:<p>5'(R)-C-Methylguanosine is a Nucleoside Derivative - 5'-Modified nucleoside.</p>Formula:C11H15N5O5Color and Shape:SolidMolecular weight:297.275’(R)-C-Methylguanosine
CAS:<p>5’-C-Methylguanosine (5’-GMG) is a nucleoside that is the major product of viral RNA replication. It has been shown to be effective against tobacco mosaic virus and other plant viruses, including strains resistant to other nucleosides. 5’-GMG can be used in combination with other antiviral agents as an inoculant or as a systemic agent for treatment of plants infected with viruses. The sensitivity of cowpea chlorotic mottle virus to 5’-GMG was found to be dependent on the strain of the virus. Incubation of infected leaves with 5’-GMG resulted in a greater number of chlorotic lesions than incubation with water or uninfected leaves.</p>Purity:Min. 95%

