2,5-Anhydro sugar diacid and 2,5-anhydro sugar diamine based C2 symmetric peptidomimetics as potential HIV-1 protease inhibitors
- 8 December 2000
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 41 (51) , 10121-10125
- https://doi.org/10.1016/s0040-4039(00)01803-7
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- Synthesis and Conformational Studies of Peptidomimetics Containing Furanoid Sugar Amino Acids and a Sugar DiacidThe Journal of Organic Chemistry, 2000
- Quantitative Symmetry in Structure−Activity Correlations: The Near C2 Symmetry of Inhibitor/HIV Protease ComplexesJournal of the American Chemical Society, 2000
- Folded Conformation in Peptides Containing Furanoid Sugar Amino AcidsJournal of the American Chemical Society, 1998
- Design and Synthesis of New PotentC2-Symmetric HIV-1 Protease Inhibitors. Use ofl-Mannaric Acid as a Peptidomimetic ScaffoldJournal of Medicinal Chemistry, 1998
- HIV-1 Protease Inhibitors Based on Acyclic CarbohydratesThe Journal of Organic Chemistry, 1998
- The Marketplace of HIV/AID$Science, 1996
- Stereoselective Synthesis of HIV-1 Protease Inhibitor, DMP 323The Journal of Organic Chemistry, 1996
- Carbohydrates and glycoconjugatesCurrent Opinion in Structural Biology, 1995
- Rational Design of Potent, Bioavailable, Nonpeptide Cyclic Ureas as HIV Protease InhibitorsScience, 1994
- STRUCTURE-BASED INHIBITORS OF HIV-1 PROTEASEAnnual Review of Biochemistry, 1993