Adenosine-d

• CAT Number: M011366
• CAS Number: 109923-50-4
• Molecular Formula: C10H12DN5O4
• Molecular Weight: 268.25
• Purity: ≥95%
• Synonyms: (3R,4S,5R)-2-(2-deuterio-6-imino-3H-purin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
• IUPAC Name: (2R,3R,4S,5R)-2-(2-deuterio-6-imino-3H-purin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
• InChI: InChI=1S/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/i2D
• InChIKey: OIRDTQYFTABQOQ-ASCSKKCOSA-N
• SMILES: [2H]C1=NC(=N)C2=C(N1)N(C=N2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO)O)O

Adenosine-d（Cat No.:M011366）refers to a deuterium-labeled form of adenosine, a purine nucleoside involved in numerous physiological processes, including energy transfer, signal transduction, and neurotransmission. The deuterium substitution enhances its stability and enables precise detection in mass spectrometry, making it highly valuable for pharmacokinetic, metabolic, and receptor-binding studies. Adenosine-d retains the biological function of native adenosine, interacting with adenosine receptors (A1, A2A, A2B, A3) to regulate cardiovascular, neurological, and immune responses. It is widely used in tracer studies to investigate nucleotide metabolism, drug interactions, and the modulation of adenosinergic signaling pathways in research and development.