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A structurally biased combinatorial approach for discovering new anti-picornaviral compounds. |
Chem Biol |
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Tsang SK;Cheh J;Isaacs L;Joseph-McCarthy D;Choi SK;Pevear DC;Whitesides GM;Hogle JM |
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Use of MCSS to design small targeted libraries: application to picornavirus ligands. |
J Am Chem Soc |
2001 |
Joseph-McCarthy D;Tsang SK;Filman DJ;Hogle JM;Karplus M |
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Structure-based design of a parallel synthetic array directed toward the discovery of irreversible inhibitors of human rhinovirus 3C protease. |
J Med Chem |
2002 |
Johnson TO;Hua Y;Luu HT;Brown EL;Chan F;Chu SS;Dragovich PS;Eastman BW;Ferre RA;Fuhrman SA;Hendrickson TF;Maldonado FC;Matthews DA;Meador JW 3rd;Patick AK;Reich SH;Skalitzky DJ;Worland ST;Yang M;Zalman LS |
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Recent advances in the synthesis, design and selection of cysteine protease inhibitors. |
Curr Opin Chem Biol |
2002 |
Hernandez AA;Roush WR |
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