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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Isaac O. Donkor

Department of Pharmaceutical Sciences

University of Tennessee Health Science Center

Memphis

Tennessee 38163

USA

[email]@utmem.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Pharmaceutical Sciences, University of Tennessee Health Science Center, Memphis, Tennessee 38163, USA. 2000 - 2008

References

  1. Structural basis for the potent calpain inhibitory activity of peptidyl alpha-ketoacids. Donkor, I.O., Assefa, H., Liu, J. J. Med. Chem. (2008) [Pubmed]
  2. Design, synthesis, molecular modeling studies, and calpain inhibitory activity of novel alpha-ketoamides incorporating polar residues at the P1'-position. Donkor, I.O., Han, J., Zheng, X. J. Med. Chem. (2004) [Pubmed]
  3. Peptidyl aldehyde inhibitors of calpain incorporating P2-proline mimetics. Donkor, I.O., Korukonda, R., Huang, T.L., LeCour, L. Bioorg. Med. Chem. Lett. (2003) [Pubmed]
  4. Trypanocidal activity of conformationally restricted pentamidine congeners. Donkor, I.O., Huang, T.L., Tao, B., Rattendi, D., Lane, S., Vargas, M., Goldberg, B., Bacchi, C. J. Med. Chem. (2003) [Pubmed]
  5. Synthesis and DHFR inhibitory activity of a series of 6-substituted-2,4-diaminothieno[2,3-d]pyrimidines. Donkor, I.O., Li, H., Queener, S.F. Eur. J. Med. Chem (2003) [Pubmed]
  6. Significance of hydrogen bonding at the S(1)' subsite of calpain I. Donkor, I.O., Zheng, X., Han, J., Lacy, C., Miller, D.D. Bioorg. Med. Chem. Lett. (2001) [Pubmed]
  7. Trypanocidal activity of dicationic compounds related to pentamidine. Donkor, I.O., Assefa, H., Rattendi, D., Lane, S., Vargas, M., Goldberg, B., Bacchi, C. Eur. J. Med. Chem (2001) [Pubmed]
  8. Asymmetric synthesis of 2,3-methanoleucine stereoisomers from common intermediates. Donkor, I.O., Zheng, X., Han, J., Miller, D.D. Chirality (2000) [Pubmed]
  9. A survey of calpain inhibitors. Donkor, I.O. Curr. Med. Chem. (2000) [Pubmed]
  10. Synthesis and calpain inhibitory activity of alpha-ketoamides with 2,3-methanoleucine stereoisomers at the P2 position. Donkor, I.O., Zheng, X., Miller, D.D. Bioorg. Med. Chem. Lett. (2000) [Pubmed]
 
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