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CAS 163706-52-3

:

Adenosine, N-acetyl-2-[(3,3,3-trifluoropropyl)thio]-, 2′,3′,5′-triacetate

Description:
Adenosine, N-acetyl-2-[(3,3,3-trifluoropropyl)thio]-, 2′,3′,5′-triacetate, identified by CAS number 163706-52-3, is a modified nucleoside derivative of adenosine. This compound features a trifluoropropylthio group, which enhances its lipophilicity and may influence its biological activity. The presence of multiple acetyl groups indicates that it has been chemically modified to potentially improve its stability or solubility in various environments. The trifluoropropyl moiety can impart unique electronic properties, making it of interest in medicinal chemistry and drug design. This compound may exhibit various pharmacological effects, including potential roles in cellular signaling or as a therapeutic agent. Its structural modifications suggest that it could interact with biological targets differently than unmodified adenosine, potentially leading to altered pharmacokinetics and pharmacodynamics. As with many nucleoside analogs, understanding its characteristics requires consideration of its synthesis, reactivity, and interactions within biological systems.
Formula:C21H24F3N5O8S
InChI:InChI=1S/C21H24F3N5O8S/c1-9(30)26-17-14-18(28-20(27-17)38-6-5-21(22,23)24)29(8-25-14)19-16(36-12(4)33)15(35-11(3)32)13(37-19)7-34-10(2)31/h8,13,15-16,19H,5-7H2,1-4H3,(H,26,27,28,30)/t13-,15-,16-,19-/m1/s1
InChI key:InChIKey=VTLARMXNHDPRLY-NVQRDWNXSA-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(NC(C)=O)N=C(SCCC(F)(F)F)N3
Synonyms:
  • Adenosine, N-acetyl-2-[(3,3,3-trifluoropropyl)thio]-, 2′,3′,5′-triacetate
  • Cangrelor Impurity 2Q: What is
  • Cangrelor Impurity 11
  • Cangrelor Impurity 2
  • Adenosine,N-acetyl-2-[(3,3,3-trifluoropropyl)thio]-,2',3',5'-triacetate (9CI)
  • Cangrelor Impurity 2 Q: What is the CAS Number of
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