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Design and synthesis of irreversible depsipeptidyl human rhinovirus 3C protease inhibitors. |
Bioorg Med Chem Lett |
2001 |
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Synthesis of new compounds with promising antiviral properties against group A and B Human Rhinoviruses. |
Bioorg Med Chem |
2014 |
Bernard AM;Cabiddu MG;De Montis S;Mura R;Pompei R |
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Design, synthesis, and evaluation of nonpeptidic inhibitors of human rhinovirus 3C protease. |
J Med Chem |
1996 |
Webber SE;Tikhe J;Worland ST;Fuhrman SA;Hendrickson TF;Matthews DA;Love RA;Patick AK;Meador JW;Ferre RA;Brown EL;DeLisle DM;Ford CE;Binford SL |
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Tripeptide aldehyde inhibitors of human rhinovirus 3C protease: design, synthesis, biological evaluation, and cocrystal structure solution of P1 glutamine isosteric replacements. |
J Med Chem |
1998 |
Webber SE;Okano K;Little TL;Reich SH;Xin Y;Fuhrman SA;Matthews DA;Love RA;Hendrickson TF;Patick AK;Meador JW 3rd;Ferre RA;Brown EL;Ford CE;Binford SL;Worland ST |
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