CAS 89178-21-2
:Adenosine, 2-bromo-2′-deoxy-
Description:
Adenosine, 2-bromo-2′-deoxy- (CAS 89178-21-2) is a modified nucleoside that features a bromine atom substituted at the 2-position of the deoxyribose sugar moiety. This compound retains the purine base adenine, which is integral to various biological processes, including energy transfer and signal transduction. The presence of the bromine atom can influence the compound's biochemical properties, potentially affecting its interaction with enzymes and receptors. Typically, such modifications can alter the nucleoside's stability, solubility, and biological activity. Adenosine derivatives are often studied for their roles in pharmacology and biochemistry, particularly in relation to their effects on cellular signaling pathways. The compound may exhibit unique properties in terms of binding affinity and efficacy compared to its unmodified counterparts. As with many nucleoside analogs, it may also have potential therapeutic applications, particularly in the fields of antiviral and anticancer research.
Formula:C10H12BrN5O3
InChI:InChI=1S/C10H12BrN5O3/c11-10-14-8(12)7-9(15-10)16(3-13-7)6-1-4(18)5(2-17)19-6/h3-6,17-18H,1-2H2,(H2,12,14,15)/t4-,5+,6+/m0/s1
InChI key:InChIKey=UYDKYWTWCPKLJR-KVQBGUIXSA-N
SMILES:NC1=C2C(N(C=N2)[C@@H]3O[C@H](CO)[C@@H](O)C3)=NC(Br)=N1
Synonyms:- 2-Bromo-2′-deoxyadenosine
- 9H-purin-6-amine, 2-bromo-9-(2-deoxypentofuranosyl)-
- Adenosine, 2-bromo-2′-deoxy-
- NSC 341936
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Found 2 products.
2-Bromo-2'-deoxyadenosine
CAS:<p>2-Bromo-2'-deoxyadenosine is a Nucleoside Derivative - Halo-nucleoside; 2-Modified purine nucleoside; Scaffold and Template.</p>Formula:C10H12BrN5O3Color and Shape:SolidMolecular weight:330.14

