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CAS 722515-03-9

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2’-Chloro-N6-(4-trifluoromethyl)benzyl adenosine

Description:
2’-Chloro-N6-(4-trifluoromethyl)benzyl adenosine, with the CAS number 722515-03-9, is a synthetic derivative of adenosine, a nucleoside that plays a crucial role in cellular energy transfer and signaling. This compound features a chloro substituent at the 2' position and a trifluoromethyl group at the para position of the benzyl moiety attached to the N6 position of the adenine base. The presence of the trifluoromethyl group enhances lipophilicity and may influence the compound's biological activity and receptor binding affinity. Typically, such modifications can affect the pharmacokinetics and pharmacodynamics of the molecule, potentially leading to increased selectivity for adenosine receptors. This compound is of interest in medicinal chemistry and pharmacology, particularly in the context of developing therapeutics for conditions influenced by adenosine signaling, such as cardiovascular diseases and cancer. Its unique structural features may also provide insights into structure-activity relationships within the adenosine receptor family.
Formula:C18H17ClF3N5O4
Synonyms:
  • 2’-Chloro-N6-(4-trifluoromethyl)benzyl adenosine
  • Adenosine, 2-chloro-N-[[4-(trifluoromethyl)phenyl]methyl]- (9CI)
  • 2’-Chloro-N6-(4-trifluoromethyl)benzyladenosine
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