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1.
Synthesis and evaluation of nitroheterocyclic phosphoramidates as hypoxia-selective alkylating agents.
J Med Chem
; 43(11): 2258-65, 2000 Jun 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-10841804
2.
Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 4. Incorporation of P1 lactam moieties as L-glutamine replacements.
J Med Chem
; 42(7): 1213-24, 1999 Apr 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-10197965
3.
Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 1. Michael acceptor structure-activity studies.
J Med Chem
; 41(15): 2806-18, 1998 Jul 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-9667970
4.
Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 2. Peptide structure-activity studies.
J Med Chem
; 41(15): 2819-34, 1998 Jul 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-9667971
5.
Structure-based design of irreversible, tripeptidyl human rhinovirus 3C protease inhibitors containing N-methyl amino acids.
Bioorg Med Chem Lett
; 9(15): 2189-94, 1999 Aug 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-10465543
6.
Design and synthesis of irreversible depsipeptidyl human rhinovirus 3C protease inhibitors.
Bioorg Med Chem Lett
; 11(20): 2683-6, 2001 Oct 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-11591501
7.
Structure-assisted design of mechanism-based irreversible inhibitors of human rhinovirus 3C protease with potent antiviral activity against multiple rhinovirus serotypes.
Proc Natl Acad Sci U S A
; 96(20): 11000-7, 1999 Sep 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-10500114
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