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Effect of the extent of thiolation and introduction of phosphorothioate internucleotide linkages on the anti-HIV activity of Suligovir [(s4dU)35].
- Source :
-
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2006 Oct 15; Vol. 16 (20), pp. 5321-3. Date of Electronic Publication: 2006 Aug 22. - Publication Year :
- 2006
-
Abstract
- Suligovir is a 35-mer homo-oligonucleotide, containing exclusively 4-thio deoxyuridylate, proved to be a potent inhibitor of HIV entry. In this paper, we described the effect of extent of thiolation and the introduction of nuclease-resistant phosphorothioate linkages on the anti-HIV activity of Suligovir. We found that the decreased thiolated nucleotide content decreases the anti-HIV potency of the compound and the introduction of phosphorothioate linkages does not improve its antiviral activity.
- Subjects :
- Anti-HIV Agents chemistry
Deoxyuracil Nucleotides chemistry
Deoxyuracil Nucleotides pharmacology
Microbial Sensitivity Tests
Molecular Structure
Oligonucleotides chemistry
Structure-Activity Relationship
Thionucleotides chemical synthesis
Thionucleotides pharmacology
Anti-HIV Agents chemical synthesis
Anti-HIV Agents pharmacology
Deoxyuracil Nucleotides chemical synthesis
HIV drug effects
Oligonucleotides chemical synthesis
Oligonucleotides pharmacology
Thionucleotides chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 0960-894X
- Volume :
- 16
- Issue :
- 20
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry letters
- Publication Type :
- Academic Journal
- Accession number :
- 16920358
- Full Text :
- https://doi.org/10.1016/j.bmcl.2006.07.082