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CAS 114748-70-8

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7-Deaza-2',3'-Dideoxy-7-Iodo-Adenosine

Description:
7-Deaza-2',3'-Dideoxy-7-Iodo-Adenosine is a modified nucleoside analog of adenosine, characterized by the substitution of a nitrogen atom in the purine ring, which enhances its stability and alters its biological activity. The presence of the iodine atom at the 7-position contributes to its unique properties, potentially influencing its interaction with nucleic acid structures and enzymes. This compound is typically used in biochemical research and drug development, particularly in studies related to antiviral and anticancer therapies, due to its ability to mimic natural nucleosides while exhibiting altered pharmacological profiles. Its structural modifications can affect its solubility, binding affinity, and metabolic stability, making it a valuable tool in the exploration of nucleoside functions and mechanisms. As with many nucleoside analogs, the specific characteristics, such as solubility and reactivity, can vary based on the surrounding conditions and the presence of other chemical entities. Overall, 7-Deaza-2',3'-Dideoxy-7-Iodo-Adenosine represents an important compound in the field of medicinal chemistry and molecular biology.
Formula:C11H13IN4O2
InChI:InChI=1S/C11H13IN4O2/c12-7-3-16(8-2-1-6(4-17)18-8)11-9(7)10(13)14-5-15-11/h3,5-6,8,17H,1-2,4H2,(H2,13,14,15)/t6-,8+/m0/s1
InChI key:OEZWDZXBBPSXGY-POYBYMJQSA-N
SMILES:C1C[C@@H](O[C@@H]1CO)N2C=C(C3=C(N=CN=C32)N)I
Synonyms:
  • 7-Deaza-2',3'-Dideoxy-7-Iodo-Adenosine
  • (2S,5R)-5-(4-Amino-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-7-yl)tetrahydro-2-furanmethanol
  • ((2S,5R)-5-(4-Amino-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-7-yl)tetrahydrofuran-2-yl)methanol
  • 7-I-7-Deaza-ddA
  • 2-Furanmethanol, 5-(4-amino-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-7-yl)tetrahydro-, (2S,5R)-
  • 7-Deaza-2',3'-Dideoxy-7-Iodo-D-Adenosine
  • 2-Furanmethanol, 5-(4-amino-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-7-yl)tetrahydro-, (2S,5R)-7-Deaza-2', 3'-dideoxy-7-iodoadenosine
  • 7-Deaza-7-Iodo-2',3'-dideoxyadenosine
  • 7-Deaza-7-I-ddA
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