CAS 524-69-6

9-β-D-Xylofuranosyladenine

Description:

9-β-D-Xylofuranosyladenine, also known by its CAS number 524-69-6, is a nucleoside analog characterized by the presence of a xylofuranosyl sugar moiety linked to an adenine base. This compound features a β-glycosidic bond, which is significant for its biological activity. The xylofuranosyl configuration distinguishes it from other nucleosides, as it can influence the compound's interaction with nucleic acid structures and enzymes. It is known to exhibit potential antiviral and anticancer properties, making it of interest in medicinal chemistry and pharmacology. The structural modifications in the sugar component can affect the stability, solubility, and overall bioavailability of the compound. Additionally, 9-β-D-Xylofuranosyladenine may participate in various biochemical pathways, potentially serving as a substrate or inhibitor for specific enzymes. Its unique characteristics make it a valuable compound for research in nucleoside chemistry and its applications in therapeutic development.

Formula: C₁₀H₁₃N₅O₄

InChI: InChI=1/C10H13N5O4/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(18)6(17)4(1-16)19-10/h2-4,6-7,10,16-18H,1H2,(H2,11,12,13)/t4-,6+,7-,10+/m1/s1

InChI key: InChIKey=OIRDTQYFTABQOQ-GAWUUDPSSA-N

SMILES: O[C@H]1[C@H](N2C=3C(N=C2)=C(N)N=CN3)O[C@H](CO)[C@@H]1O

Synonyms:

• 9-.alpha.-D-Xylofuranosyladenine
• 9-β-<span class="text-smallcaps">D</span>-Xylofuranosyl-9H-purin-6-amine
• 9-β-<span class="text-smallcaps">D</span>-Xylofuranosyladenine
• 9H-Purin-6-amine, 9-.alpha.-D-xylofuranosyl-
• 9H-Purin-6-amine, 9-β-<span class="text-smallcaps">D</span>-xylofuranosyl-
• Adenine xyloside
• Adenine β-<span class="text-smallcaps">D</span>-xylofuranoside
• Adenine, 9-.alpha.-D-xylofuranosyl-
• Adenine, 9-β-<span class="text-smallcaps">D</span>-xylofuranosyl-
• Adenine-9-β-<span class="text-smallcaps">D</span>-xylofuranoside
• Amg 002370
• NSC 7359
• Nqz-007
• Xyloadenosine
• Xylosyladenine
• 9-β-D-Xylofuranosyladenine
• 9H-Purin-6-amine, 9-β-D-xylofuranosyl-
• 9-β-D-Xylofuranosyl-9H-purin-6-amine
• Adenine, 9-β-D-xylofuranosyl-
• Xylosyl a
• Adenine, 9-.beta.-D-xylofuranosyl-
• Xa
• Xylo-adenosine
• 9H-Purin-6-amine, 9-.beta.-D-xylofuranosyl-
• 9-(-D-Xylofuranosyl)adenine
• 9-.beta.-D-Xylofuranosyladenine
• 9-(b-D-Xylofuranosyl)adenine,Xylo-adenosine, anticancer agent
• 9-(b-D-Xylofuranosyl)adenine

9-(β-D-Xylofuranosyl)adenine

CAS: 524-69-6

9-(β-D-Xylofuranosyl)adenine

Purity: ≥98%

Molecular weight: 267.24g/mol

Ref: 54-BUP06690

9-(β-D-Xylofuranosyl)adenine

CAS: 524-69-6

9-(β-D-Xylofuranosyl)adenine (Adenine xyloside) is an adenine nucleoside analog that is a potential smooth muscle vasodilator.9-(β-D-Xylofuranosyl)adenine has

Formula: C₁₀H₁₃N₅O₄

Purity: 99.97%

Color and Shape: Solid

Molecular weight: 267.24

Ref: TM-TNU0266

9-(β-D-Xylofuranosyl)adenine

CAS: 524-69-6

9-(β-D-Xylofuranosyl)adenine is a nucleoside analog that inhibits the activity of adenine nucleotide. It has been shown to be effective against a wide range of viruses and bacteria, including HIV, herpes simplex virus, influenza A virus, and Mycobacterium tuberculosis. The chemical structure of 9-(β-D-Xylofuranosyl)adenine resembles that of adenosine and this similarity confers inhibitory properties on it. 9-(β-D-Xylofuranosyl)adenine is an analog of adenosine. The steric interactions between the intramolecular hydrogen bonds in 9-(β-D-Xylofuranosyl)adenine are weaker than those in adenosine, which allows it to bind more easily with the enzyme responsible for the conversion of adenosine to inosinic acid. This inhibition prevents the formation of ATP from AMP, leading

Formula: C₁₀H₁₃N₅O₄

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 267.24 g/mol

Ref: 3D-FX144729