CAS 3969-27-5
:8-methoxy-9-pentofuranosyl-9H-purin-6-amine
Description:
8-Methoxy-9-pentofuranosyl-9H-purin-6-amine, with the CAS number 3969-27-5, is a purine derivative that exhibits characteristics typical of nucleosides. This compound features a purine base, which is a fundamental component of nucleic acids, and is modified with a methoxy group at the 8-position and a pentofuranosyl sugar moiety. The presence of the methoxy group can influence its solubility and biological activity, potentially enhancing its stability and interaction with biological targets. As a nucleoside analog, it may exhibit antiviral or anticancer properties, making it of interest in medicinal chemistry. The structural modifications can affect its pharmacokinetics, including absorption, distribution, metabolism, and excretion. Additionally, the compound's ability to participate in hydrogen bonding and its electronic properties can influence its interactions with enzymes and receptors. Overall, 8-methoxy-9-pentofuranosyl-9H-purin-6-amine represents a significant class of compounds that can be explored for therapeutic applications in various biological contexts.
Formula:C11H15N5O5
InChI:InChI=1/C11H15N5O5/c1-20-11-15-5-8(12)13-3-14-9(5)16(11)10-7(19)6(18)4(2-17)21-10/h3-4,6-7,10,17-19H,2H2,1H3,(H2,12,13,14)
SMILES:COc1nc2c(N)ncnc2n1C1C(C(C(CO)O1)O)O
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Found 2 products.
8-Methoxyadenosine
CAS:<p>8-Methoxyadenosine is a Nucleoside Derivative - 8-Modified purine nucleoside.</p>Formula:C11H15N5O5Color and Shape:SolidMolecular weight:297.278-Methoxyadenosine
CAS:<p>8-Methoxyadenosine is an acidic adenosine that acts as a competitive antagonist of the A1 receptor. It has a high affinity for this receptor and blocks the binding of adenosine to the receptor, thereby inhibiting its function. 8-Methoxyadenosine is also a competitive antagonist of the uridine nucleotide, which inhibits enzymatic catalysis by ribonucleoside kinase and ribonucleotide reductase. It has been shown to have properties similar to those of other pyrimidine nucleosides such as cytidine, thymine, and uridine. This molecule has a hydroxyl group in its structure, which is essential for binding to these enzymes. 8-Methoxyadenosine also has a phosphate group in its structure, which is necessary for the synthesis of DNA or RNA from deoxyribonucleotides. The benzoate group in 8-methoxyadenosine's structure makes</p>Purity:Min. 95%

