CAS 146-78-1: 2-Fluoroadenosine
Description:2-Fluoroadenosine is a modified nucleoside that features a fluorine atom substituted at the 2-position of the adenine base. Its molecular formula is C10H12FN5O3, and it is classified as a purine nucleoside, which is a building block of nucleic acids. This compound is known for its potential applications in biochemistry and pharmacology, particularly in the study of nucleoside analogs and their effects on cellular processes. The presence of the fluorine atom can influence the compound's biological activity, stability, and interaction with enzymes and receptors. 2-Fluoroadenosine is often used in research to explore mechanisms of action in cellular signaling pathways and to investigate its potential as an antiviral or anticancer agent. Its solubility and reactivity can vary depending on the conditions, making it a subject of interest in medicinal chemistry. As with many nucleoside analogs, understanding its pharmacokinetics and biological effects is crucial for developing therapeutic applications.
Formula:C10H12FN5O4
InChI:InChI=1S/C10H12FN5O4/c11-10-14-7(12)4-8(15-10)16(2-13-4)9-6(19)5(18)3(1-17)20-9/h2-3,5-6,9,17-19H,1H2,(H2,12,14,15)/t3-,5-,6-,9-/m1/s1
InChI key:InChIKey=HBUBKKRHXORPQB-UUOKFMHZSA-N
SMILES:FC=1N=C(N)C=2N=CN(C2N1)C3OC(CO)C(O)C3O
- Synonyms:
- 2-Fluoro-9-β-<span class="text-smallcaps">D</span>-ribofuranosyladenine
- 2-Fluoroadenosine
- 2-fluoro-9-pentofuranosyl-9H-purin-6-amine
- Adenosine, 2-fluoro-
- NSC 30605
- 2-Fluoro-9-β-D-ribofuranosyladenine
