Tripeptide Aldehyde Inhibitors of Human Rhinovirus 3C Protease:  Design, Synthesis, Biological Evaluation, and Cocrystal Structure Solution of P 1 Glutamine Isosteric Replacements

Tripeptide Aldehyde Inhibitors of Human Rhinovirus 3C Protease:  Design, Synthesis, Biological Evaluation, and Cocrystal Structure Solution of P 1 Glutamine Isosteric Replacements

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Veröffentlicht in:Journal of medicinal chemistry 1998-07, Vol.41 (15), p.2786-2805
Hauptverfasser: Webber, Stephen E., Okano, Koji, Little, Thomas L., Reich, Siegfried H., Xin, Yue, Fuhrman, Shella A., Matthews, David A., Love, Robert A., Hendrickson, Thomas F., Patick, Amy K., Meador, James W., Ferre, Rose Ann, Brown, Edward L., Ford, Clifford E., Binford, Susan L., Worland, Stephen T.
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container_end_page 2805
container_issue 15
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container_title Journal of medicinal chemistry
container_volume 41
creator Webber, Stephen E.
Okano, Koji
Little, Thomas L.
Reich, Siegfried H.
Xin, Yue
Fuhrman, Shella A.
Matthews, David A.
Love, Robert A.
Hendrickson, Thomas F.
Patick, Amy K.
Meador, James W.
Ferre, Rose Ann
Brown, Edward L.
Ford, Clifford E.
Binford, Susan L.
Worland, Stephen T.
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doi_str_mv 10.1021/jm980071x
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title Tripeptide Aldehyde Inhibitors of Human Rhinovirus 3C Protease:  Design, Synthesis, Biological Evaluation, and Cocrystal Structure Solution of P 1 Glutamine Isosteric Replacements
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