For research use only. Not for therapeutic Use.
2-Amino Adenosine (Cat.No:R003119) is a modified form of adenosine, a nucleoside found in RNA. The addition of an amino group makes it valuable in biochemical research. It is used to study adenosine receptor activity and has potential applications in drug development, particularly in the field of neurological disorders and cancer therapy.
Catalog Number | R003119 |
CAS Number | 2096-10-8 |
Synonyms | 2,6-Diamino-9-β-D-ribofuranosyl-9H-purine; 2,6-Diaminonebularine; 9-β-Ribosyl-2,6-diaminopurine; 2,6-Diaminopurine Riboside; 2,6-Diaminopurinosine; NSC 7363; |
Molecular Formula | C10H14N6O4 |
Purity | ≥95% |
Target | Nucleoside Antimetabolite/Analog |
Storage | Store at -20°C |
IUPAC Name | (2R,3R,4S,5R)-2-(2,6-diaminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol |
InChI | InChI=1S/C10H14N6O4/c11-7-4-8(15-10(12)14-7)16(2-13-4)9-6(19)5(18)3(1-17)20-9/h2-3,5-6,9,17-19H,1H2,(H4,11,12,14,15)/t3-,5-,6-,9-/m1/s1 |
InChIKey | ZDTFMPXQUSBYRL-UUOKFMHZSA-N |
SMILES | C1=NC2=C(N1C3C(C(C(O3)CO)O)O)N=C(N=C2N)N |
Reference | <span style=”font-size:12px;”><span style=”font-family:arial,helvetica,sans-serif;”>1.Long, Mary C., Vincent Escuyer, and William B. Parker. "Identification and characterization of a unique adenosine kinase from Mycobacterium tuberculosis." <i style=”font-family: Arial, sans-serif; font-size: 13px;”>Journal of bacteriology</i> 185.22 (2003): 6548-6555.<br /> |