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- [33] Flexible docking, synthesis and biological evaluation of N-[(4-pyrazolyl)cyclopropylmethyl] cyclic ureas as HIV protease inhibitors. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1998, 215 : U868 - U868
- [35] Synthesis of highly potent HIV protease inhibitors with activity against protease resistant virus. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2002, 224 : U9 - U9
- [36] SYNTHESIS, STRUCTURE-ACTIVITY RELATIONSHIP AND X-RAY STUDIES OF POTENT NONPEPTIDAL CYCLIC HIV PROTEASE INHIBITORS ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1994, 208 : 36 - MEDI
- [37] Structure activity relationship of cyclic ureas with asymmetric P2/P2' substituents: Potent inhibitors of HIV-1 protease. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1997, 213 : 306 - MEDI
- [40] DESIGN AND SYNTHESIS OF POTENT, ORALLY BIOAVAILABLE HIV-1 PROTEASE INHIBITORS ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1994, 208 : 17 - MEDI