Authors:
Reich, SH
Johnson, T
Wallace, MB
Kephart, SE
Fuhrman, SA
Worland, ST
Matthews, DA
Hendrickson, TF
Chan, F
Meador, J
Ferre, RA
Brown, EL
DeLisle, DM
Patick, AK
Binford, SL
Ford, CE
Citation: Sh. Reich et al., Substituted benzamide inhibitors of human rhinovirus 3C protease: Structure-based design, synthesis, and biological evaluation, J MED CHEM, 43(9), 2000, pp. 1670-1683
Authors:
Matthews, DA
Dragovich, PS
Webber, SE
Fuhrman, SA
Patick, AK
Zalman, LS
Hendrickson, TF
Love, RA
Prins, TJ
Marakovits, JT
Zhou, R
Tikhe, J
Ford, CE
Meador, JW
Ferre, RA
Brown, EL
Binford, SL
Brothers, MA
DeLisle, DM
Worland, ST
Citation: Da. Matthews et al., Structure-assisted design of mechanism-based irreversible inhibitors of human rhinovirus 3C protease with potent antiviral activity against multiple rhinovirus serotypes, P NAS US, 96(20), 1999, pp. 11000-11007
Authors:
Dragovich, PS
Prins, TJ
Zhou, R
Webber, SE
Marakovits, JT
Fuhrman, SA
Patick, AK
Matthews, DA
Lee, CA
Ford, CE
Burke, BJ
Rejto, PA
Hendrickson, TF
Tuntland, T
Brown, EL
Meador, JW
Ferre, RA
Harr, JEV
Kosa, MB
Worland, ST
Citation: Ps. Dragovich et al., Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 4. Incorporation of P-1 lactam moieties as L-glutamine replacements, J MED CHEM, 42(7), 1999, pp. 1213-1224