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CAS 15811-32-2

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Adenosine, 2-fluoro-, 2′,3′,5′-triacetate

Description:
Adenosine, 2-fluoro-, 2′,3′,5′-triacetate, with the CAS number 15811-32-2, is a modified nucleoside derivative of adenosine. This compound features a fluorine atom at the 2-position of the ribose sugar, which can influence its biological activity and stability. The presence of three acetyl groups at the 2′, 3′, and 5′ positions enhances its lipophilicity, potentially facilitating cellular uptake and altering its interaction with biological targets. The modification of adenosine in this manner can affect its role in biochemical pathways, particularly in relation to nucleic acid synthesis and signaling. As a chemical entity, it may exhibit unique pharmacological properties, making it of interest in medicinal chemistry and biochemistry research. Its solubility, reactivity, and stability can vary based on environmental conditions, such as pH and temperature. Overall, this compound serves as a valuable tool for studying nucleoside function and for developing therapeutic agents targeting adenosine receptors or related pathways.
Formula:C16H18FN5O7
InChI:InChI=1S/C16H18FN5O7/c1-6(23)26-4-9-11(27-7(2)24)12(28-8(3)25)15(29-9)22-5-19-10-13(18)20-16(17)21-14(10)22/h5,9,11-12,15H,4H2,1-3H3,(H2,18,20,21)/t9-,11-,12-,15-/m1/s1
InChI key:InChIKey=LDICZLRLPNWOIS-SDBHATRESA-N
SMILES:O(C(C)=O)[C@H]1[C@@H](O[C@H](COC(C)=O)[C@H]1OC(C)=O)N2C=3C(N=C2)=C(N)N=C(F)N3
Synonyms:
  • 2-Fluoro-2',3',5'-tri-o-acetyladenosine
  • 2-Fluoro-2',3',5'-triacetoxyadenosine
  • 2-Fluoro-2,3,5'-tri-o-acetyladenosine
  • 2′,3′,5′-Tri-O-acetyl-2-fluoroadenosine
  • Adenosine, 2-fluoro-, 2′,3′,5′-triacetate
  • NSC 108853
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