共 50 条
- [21] Synthesis of 1-aryl-7-substituted phthalazines as parasite cysteine protease inhibitors. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2003, 225 : U193 - U193
- [22] STRUCTURE-BASED DESIGN OF CALCINEURIN INHIBITORS. ACTA CRYSTALLOGRAPHICA A-FOUNDATION AND ADVANCES, 1996, 52 : C201 - C201
- [23] Structure-based design of ricin inhibitors. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2000, 219 : U54 - U54
- [24] Design, synthesis and SAR analysis of anthrax lethal factor protease inhibitors. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2004, 228 : U955 - U955
- [26] Structure-based design of ketone-containing human rhinovirus 3C protease inhibitors. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2000, 219 : U3 - U3
- [27] Structure-based design of irreversible peptidyl and peptidomimetic human rhinovirus 3C protease inhibitors. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1999, 217 : U1233 - U1233
- [28] Comparative QSAR as a cheminformatics tool in the design of HIV-1 protease inhibitors. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2005, 229 : U778 - U779
- [29] Recent advances in the design, synthesis and molecular recognition of cyclic HIV protease inhibitors. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1996, 212 : 122 - MEDI
- [30] Structure-biased library design:: α-ketoamide inhibitors of cruzain, a cysteine protease involved in Chagas' disease RATIONAL APPROACHES TO DRUG DESIGN, 2001, : 65 - 68