Danielle Skropeta

Summary

Affiliation: University of Wollongong
Country: Australia

Publications

  1. ncbi Kinase inhibitors from marine sponges
    Danielle Skropeta
    School of Chemistry, University of Wollongong, Wollongong, NSW 2522, Australia
    Mar Drugs 9:2131-54. 2011
  2. ncbi Deep-sea natural products
    Danielle Skropeta
    School of Chemistry, University of Wollongong, Wollongong, Australia
    Nat Prod Rep 25:1131-66. 2008
  3. ncbi The effect of individual N-glycans on enzyme activity
    Danielle Skropeta
    School of Chemistry, University of Wollongong, Wollongong, NSW 2522, Australia
    Bioorg Med Chem 17:2645-53. 2009
  4. ncbi N-phenethyl and N-naphthylmethyl isatins and analogues as in vitro cytotoxic agents
    Lidia Matesic
    School of Chemistry, University of Wollongong, Wollongong, NSW 2522, Australia
    Bioorg Med Chem 16:3118-24. 2008
  5. ncbi Kinase inhibitory, haemolytic and cytotoxic activity of three deep-water sponges from North Western Australia and their fatty acid composition
    Ana Zivanovic
    School of Chemistry, University of Wollongong, NSW 2500, Australia
    Nat Prod Commun 6:1921-4. 2011
  6. ncbi c-AMP dependent protein kinase A inhibitory activity of six algal extracts from southeastern Australia and their fatty acid composition
    Ana Zivanovic
    School of Chemistry, University of Wollongong, NSW, 2500, Australia
    Nat Prod Commun 7:923-6. 2012
  7. ncbi N,O-isopropylidenated threonines as tools for peptide cyclization: application to the synthesis of mahafacyclin B
    Nima Sayyadi
    School of Chemistry, The University of Sydney, 2006 NSW, Australia
    Org Lett 7:5497-9. 2005

Collaborators

Detail Information

Publications7

  1. ncbi Kinase inhibitors from marine sponges
    Danielle Skropeta
    School of Chemistry, University of Wollongong, Wollongong, NSW 2522, Australia
    Mar Drugs 9:2131-54. 2011
    ..These compounds, which belong to diverse structural classes, are reviewed herein, and ordered based upon the kinase that they inhibit. Relevant synthetic studies on the marine natural product kinase inhibitors have also been included...
  2. ncbi Deep-sea natural products
    Danielle Skropeta
    School of Chemistry, University of Wollongong, Wollongong, Australia
    Nat Prod Rep 25:1131-66. 2008
    ..Relevant synthetic studies on the deep-sea natural products have also been included...
  3. ncbi The effect of individual N-glycans on enzyme activity
    Danielle Skropeta
    School of Chemistry, University of Wollongong, Wollongong, NSW 2522, Australia
    Bioorg Med Chem 17:2645-53. 2009
    ....
  4. ncbi N-phenethyl and N-naphthylmethyl isatins and analogues as in vitro cytotoxic agents
    Lidia Matesic
    School of Chemistry, University of Wollongong, Wollongong, NSW 2522, Australia
    Bioorg Med Chem 16:3118-24. 2008
    ..The results allowed further development of structure-activity relationships. The compound 5,7-dibromo-N-(1-naphthylmethyl)-1H-indole-2,3-dione 5a was the most potent against U937 cells with an IC(50) value of 0.19 microM...
  5. ncbi Kinase inhibitory, haemolytic and cytotoxic activity of three deep-water sponges from North Western Australia and their fatty acid composition
    Ana Zivanovic
    School of Chemistry, University of Wollongong, NSW 2500, Australia
    Nat Prod Commun 6:1921-4. 2011
    ....
  6. ncbi c-AMP dependent protein kinase A inhibitory activity of six algal extracts from southeastern Australia and their fatty acid composition
    Ana Zivanovic
    School of Chemistry, University of Wollongong, NSW, 2500, Australia
    Nat Prod Commun 7:923-6. 2012
    ..Importantly, this study reveals that abundant and readily available marine algae are a new and relatively unexplored source of PKA inhibitory compounds...
  7. ncbi N,O-isopropylidenated threonines as tools for peptide cyclization: application to the synthesis of mahafacyclin B
    Nima Sayyadi
    School of Chemistry, The University of Sydney, 2006 NSW, Australia
    Org Lett 7:5497-9. 2005
    ..Incorporation of an N,O-isopropylidenated threonine more than doubles the head-to-tail cyclization yield. The N,O-isopropylidene grouping is then readily disassembled to give the antimalarial cyclic peptide in high yield...