CAS 95523-13-0

N6-(P-aminobenzyl)adenosine

Description:

N6-(P-aminobenzyl)adenosine is a synthetic derivative of adenosine, characterized by the presence of a p-aminobenzyl group at the N6 position of the adenine moiety. This modification enhances its potential for biological activity, particularly in the context of adenosine receptor interactions. The compound is typically a white to off-white solid and is soluble in polar solvents, which facilitates its use in various biochemical assays and research applications. Its structure allows it to mimic adenosine, making it a valuable tool in studying adenosine signaling pathways and their implications in physiological and pathological processes. The presence of the amino group may also contribute to its reactivity and ability to form conjugates with other biomolecules. As a research chemical, N6-(P-aminobenzyl)adenosine is primarily utilized in pharmacological studies, particularly those exploring the roles of adenosine in cellular signaling, inflammation, and cancer biology. Proper handling and storage conditions are essential to maintain its stability and efficacy in experimental settings.

Formula: C₁₇H₂₀N₆O₄

InChI: InChI=1/C17H20N6O4/c18-10-3-1-9(2-4-10)5-19-15-12-16(21-7-20-15)23(8-22-12)17-14(26)13(25)11(6-24)27-17/h1-4,7-8,11,13-14,17,24-26H,5-6,18H2,(H,19,20,21)/t11-,13-,14-,17-/m1/s1

SMILES: c1cc(ccc1CNc1c2c(ncn1)n(cn2)[C@H]1[C@@H]([C@@H]([C@@H](CO)O1)O)O)N

Synonyms:

• N(6)-(4-Aminobenzyl)adenosine
• 4-Abza
• Adenosine, N-((4-aminophenyl)methyl)-
• N-(4-aminobenzyl)adenosine

N-[(4-Aminophenyl)methyl]adenosine

CAS: 95523-13-0

N-[(4-Aminophenyl)methyl]adenosine

Purity: ≥98%

Molecular weight: 372.38g/mol

Ref: 54-BUP05501

N-[(4-Aminophenyl)methyl]adenosine

CAS: 95523-13-0

N-[(4-Aminophenyl)methyl]adenosine is an adenosine receptor inhibitor (Ki: 29 nM for Rat ecto-5′-Nucleotidase).

Formula: C₁₇H₂₀N₆O₄

Purity: 98.75%

Color and Shape: Solid

Molecular weight: 372.38

Ref: TM-T16166