Research Topics
| Katherine L Seley-RadtkeSummaryAffiliation: University of Maryland Country: USA Publications
Research Grants
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Detail Information
Publications
Carbocyclic isoadenosine analogues of neplanocin AKatherine L Seley
School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, Georgia, USA
Org Lett 5:4401-3. 2003..Their design, synthesis, and structural elucidation is reported...
Design and synthesis of a series of chlorinated 3-deazaadenine analoguesKatherine L Seley
School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, Georgia, USA
Nucleosides Nucleotides Nucleic Acids 22:2133-44. 2003..During the synthetic efforts, two unexpected compounds were identified. Their synthesis, along with synthesis of the chlorinated targets is presented herein...
"Molecular chameleons". Design and synthesis of C-4-substituted imidazole fleximersKatherine L Seley
Department of Chemistry and Biochemistry, University of Maryland, Baltimore County, Baltimore, Maryland 21250, USA
Org Lett 7:63-6. 2005..As a result, these structurally innovative nucleosides can more readily adapt to capricious binding sites and, as such, should find use for investigating enzyme-coenzyme as well as nucleic acid-protein interactions...
"Molecular chameleons". Design and synthesis of a second series of flexible nucleosidesKatherine L Seley
Department of Chemistry and Biochemistry, University of Maryland, Baltimore County, Baltimore, Maryland 21250, USA
J Org Chem 70:1612-9. 2005..Their design and synthesis is described...
Carbocyclic thymidine analogues for use as potential therapeutic agentsKatherine L Seley-Radtke
Department of Chemistry and Biochemistry, University of Maryland Baltimore County, Baltimore, Maryland, USA
Nucleosides Nucleotides Nucleic Acids 28:633-41. 2009..In that regard, the synthesis and preliminary biological results for two truncated carbocyclic thymidine analogues are presented herein...
Synthetic strategies toward carbocyclic purine-pyrimidine hybrid nucleosidesJoshua M Sadler
Department of Chemistry and Biochemistry, University of Maryland, Baltimore County, 1000 Hilltop Circle, Baltimore, MD 21250, USA
Bioorg Med Chem 17:5520-5. 2009..In that regard, the design, synthesis and results of preliminary biological activity for a series of carbocyclic uracil derivatives with either a fused imidazole or thiazole ring are presented herein...
Synthesis and biological evaluation of a series of thieno-expanded tricyclic purine 2'-deoxy nucleoside analoguesOrrette R Wauchope
Department of Chemistry and Biochemistry, University of Maryland, Baltimore County, 1000 Hilltop Circle, Baltimore, MD 21250, USA
Bioorg Med Chem 20:3009-15. 2012..The synthetic efforts towards realizing the expanded 2'-deoxy-guanosine and -adenosine tricyclic analogues as well as the preliminary biological results are presented herein...
Tricyclic 2'-C-modified nucleosides as potential anti-HCV therapeuticsOrrette R Wauchope
Department of Chemistry and Biochemistry, University of Maryland, Baltimore County, 1000 Hilltop Circle, Baltimore, Maryland 21250, USA
Org Lett 12:4466-9. 2010..Details of the synthesis, structural characterization, and preliminary biological results are reported...
A computational study of expanded heterocyclic nucleosides in DNAPeter I O'Daniel
Department of Chemistry and Biochemistry, University of Maryland, Baltimore County, 1000 Hilltop Circle, Baltimore, Maryland 21250, USA
J Biomol Struct Dyn 26:283-92. 2008..MD simulations of 10-mers suggest that the balance between base pairing vs. base stacking and intercalation can be shifted towards the latter due to the increased surface area and polarizability of the expanded bases...
Carbocyclic pyrimidine nucleosides as inhibitors of S-adenosylhomocysteine hydrolaseSylvester L Mosley
Department of Chemistry and Biochemistry, University of Maryland, Baltimore County, Baltimore, MD 21250, USA
Bioorg Med Chem 14:7967-71. 2006..3.1.1) for a series of truncated carbocyclic pyrimidine nucleoside analogues is presented. Of the four nucleosides obtained, 10 was found to be active with a Ki value of 5.0 microM against SAHase...
Research Grants
- Unnatural Base Pairs as DNA BioprobesKATHERINE RADTKE; Fiscal Year: 2009..abstract_text> ..
- Unnatural Base Pairs as DNA BioprobesKATHERINE RADTKE; Fiscal Year: 2007..abstract_text> ..
- Fused Pyrimidine (IsoA) Nucleosides:Design and SynthesisKATHERINE RADTKE; Fiscal Year: 2006..We believe this inhibition will result in meaningful biological activity, as well as to induce cell differentiation. ..
