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CAS 81794-13-0

:

5′-O-[Bis(4-methoxyphenyl)phenylmethyl]-2′-O-[(1,1-dimethylethyl)dimethylsilyl]adenosine

Description:
5′-O-[Bis(4-methoxyphenyl)phenylmethyl]-2′-O-[(1,1-dimethylethyl)dimethylsilyl]adenosine, with the CAS number 81794-13-0, is a modified nucleoside derivative of adenosine. This compound features a complex structure that includes a 5′-O-bis(4-methoxyphenyl)phenylmethyl group and a 2′-O-(1,1-dimethylethyl)dimethylsilyl moiety, which enhance its stability and solubility. The presence of methoxy groups contributes to its lipophilicity, potentially influencing its biological activity and interaction with cellular targets. The silyl group provides protection against hydrolysis, making it more resistant to enzymatic degradation. Such modifications are often employed to improve the pharmacokinetic properties of nucleosides, allowing for better absorption and longer half-life in biological systems. This compound may be of interest in biochemical research, particularly in studies involving nucleoside analogs and their applications in drug development or molecular biology. Its unique structural features suggest potential utility in therapeutic contexts, although specific biological activities would require further investigation.
Formula:C37H45N5O6Si
InChI:InChI=1S/C37H45N5O6Si/c1-36(2,3)49(6,7)48-32-31(43)29(47-35(32)42-23-41-30-33(38)39-22-40-34(30)42)21-46-37(24-11-9-8-10-12-24,25-13-17-27(44-4)18-14-25)26-15-19-28(45-5)20-16-26/h8-20,22-23,29,31-32,35,43H,21H2,1-7H3,(H2,38,39,40)/t29-,31-,32-,35-/m1/s1
InChI key:InChIKey=WBXYUFMFVHCXRR-QSYCCZFCSA-N
SMILES:C(OC[C@H]1O[C@H]([C@H](O[Si](C(C)(C)C)(C)C)[C@@H]1O)N2C=3C(N=C2)=C(N)N=CN3)(C4=CC=C(OC)C=C4)(C5=CC=C(OC)C=C5)C6=CC=CC=C6
Synonyms:
  • Adenosine, 5′-O-[bis(4-methoxyphenyl)phenylmethyl]-2′-O-[(1,1-dimethylethyl)dimethylsilyl]-
  • 5′-O-[Bis(4-methoxyphenyl)phenylmethyl]-2′-O-[(1,1-dimethylethyl)dimethylsilyl]adenosine
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