Zobrazeno 1 - 3
of 3
pro vyhledávání: '"James E. V. Harr"'
Autor:
Babine Robert E, Edward L. Brown, David A. Matthews, Susan L. Binford, Stephen T. Worland, Shella A. Fuhrman, Amy K. Patick, James E. V. Harr, Reich Siegfried Heinz, Joseph T. Marakovits, Thomas J. Prins, Caroline A. Lee, Wallace Michael B, Peter S. Dragovich, Littlefield Ethel S, and Dorothy M. DeLisle, James W. Meador, Rose Ann Ferre, Clifford E. Ford, Ru Zhou, Stephen E. Webber, Jayashree Tikhe
Publikováno v:
Journal of Medicinal Chemistry. 41:2819-2834
The structure-based design, chemical synthesis, and biological evaluation of various peptide-derived human rhinovirus (HRV) 3C protease (3CP) inhibitors are described. These compounds are comprised of an ethyl propenoate Michael acceptor moiety and a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97ae4560588b9aa6544425b6ac69eedc
https://doi.org/10.1021/jm9800696
https://doi.org/10.1021/jm9800696
Autor:
Ru Zhou, Stephen E. Webber, Thomas J. Prins, Joseph T. Marakovits, Rose Ann Ferre, Edward L. Brown, Caroline A. Lee, James E. V. Harr, Peter S. Dragovich, Tove Tuntland, Benjamin J. Burke, Amy K. Patick, Clifford E. Ford, Shella A. Fuhrman, Paul A. Rejto, Thomas F. Hendrickson, Maha Kosa, Stephen T. Worland, James W. Meador, David A. Matthews
Publikováno v:
Journal of medicinal chemistry. 42(7)
The structure-based design, chemical synthesis, and biological evaluation of various human rhinovirus (HRV) 3C protease (3CP) inhibitors which incorporate P1 lactam moieties in lieu of an L-glutamine residue are described. These compounds are compris
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92c2f8160e8a7ea6fa4aba2828d373e2
https://pubmed.ncbi.nlm.nih.gov/10197965
https://pubmed.ncbi.nlm.nih.gov/10197965
Autor:
Peter S. Dragovich, Stephen E. Webber, Robert E. Babine, Shella A. Fuhrman, Amy K. Patick, David A. Matthews, Caroline A. Lee, Siegfried H. Reich, Thomas J. Prins, Joseph T. Marakovits, Ethel S. Littlefield, Ru Zhou, Jayashree Tikhe, Clifford E. Ford, Michael B. Wallace, James W. Meador, Rose Ann Ferre, Edward L. Brown, Susan L. Binford, James E. V. Harr, Dorothy M. DeLisle, Stephen T. Worland
Publikováno v:
Journal of medicinal chemistry. 41(15)
The structure-based design, chemical synthesis, and biological evaluation of peptide-derived human rhinovirus (HRV) 3C protease (3CP) inhibitors are described. These compounds incorporate various Michael acceptor moieties and are shown to irreversibl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0aa969905b2a5a25f60f0720f539ece
https://pubmed.ncbi.nlm.nih.gov/9667970
https://pubmed.ncbi.nlm.nih.gov/9667970