Click Chemistry on Azidoproline: High‐Affinity Dual Antagonist for HIV‐1 Envelope Glycoprotein gp120
- 5 January 2006
- journal article
- Published by Wiley in ChemMedChem
- Vol. 1 (1), 54-57
- https://doi.org/10.1002/cmdc.200500037
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- In Situ Click Chemistry: Enzyme Inhibitors Made to Their Own SpecificationsJournal of the American Chemical Society, 2004
- Profiling Enzyme Activities In Vivo Using Click Chemistry MethodsCell Chemical Biology, 2004
- Mode of Action for Linear Peptide Inhibitors of HIV-1 gp120 InteractionsBiochemistry, 2004
- Cell Surface Labeling of Escherichia coli via Copper(I)-Catalyzed [3+2] CycloadditionJournal of the American Chemical Society, 2003
- A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal AlkynesAngewandte Chemie, 2002
- CD4-induced interaction of primary HIV-1 gp120 glycoproteins with the chemokine receptor CCR-5Nature, 1996
- CD4-dependent, antibody-sensitive interactions between HIV-1 and its co-receptor CCR-5Nature, 1996
- A Dual-Tropic Primary HIV-1 Isolate That Uses Fusin and the β-Chemokine Receptors CKR-5, CKR-3, and CKR-2b as Fusion CofactorsCell, 1996
- T-lymphocyte T4 molecule behaves as the receptor for human retrovirus LAVNature, 1984
- The CD4 (T4) antigen is an essential component of the receptor for the AIDS retrovirusNature, 1984