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AMD3100, a small molecule inhibitor of HIV-1 entry via the CXCR4 co-receptor.
- Source :
-
Nature medicine [Nat Med] 1998 Jan; Vol. 4 (1), pp. 72-7. - Publication Year :
- 1998
-
Abstract
- The bicyclam AMD3100 (formula weight 830) blocks HIV-1 entry and membrane fusion via the CXCR4 co-receptor, but not via CCR5. AMD3100 prevents monoclonal antibody 12G5 from binding to CXCR4, but has no effect on binding of monoclonal antibody 2D7 to CCR5. It also inhibits binding of the CXC-chemokine, SDF-1alpha, to CXCR4 and subsequent signal transduction, but does not itself cause signaling and has no effect on RANTES signaling via CCR5. Thus, AMD3100 prevents CXCR4 functioning as both a HIV-1 co-receptor and a CXC-chemokine receptor. Development of small molecule inhibitors of HIV-1 entry is feasible.
- Subjects :
- Antibodies, Monoclonal pharmacology
Benzylamines
CD4 Antigens immunology
CD4 Antigens physiology
CD4-Positive T-Lymphocytes drug effects
Calcium metabolism
Carbachol pharmacology
Cell Fusion
Cell Line
Cells, Cultured
Chemokine CCL5 pharmacology
Chemokine CXCL12
Cyclams
Cytokines metabolism
Cytokines pharmacology
HIV Envelope Protein gp120 drug effects
HIV Envelope Protein gp120 metabolism
HIV-1 drug effects
Humans
Interleukin-2 pharmacology
Kinetics
Membrane Fusion drug effects
Receptors, CCR5 physiology
Receptors, CXCR4 drug effects
Receptors, CXCR4 immunology
Signal Transduction drug effects
Somatostatin pharmacology
Anti-HIV Agents pharmacology
CD4-Positive T-Lymphocytes physiology
CD4-Positive T-Lymphocytes virology
Chemokines, CXC
HIV-1 physiology
Heterocyclic Compounds pharmacology
Receptors, CXCR4 physiology
Subjects
Details
- Language :
- English
- ISSN :
- 1078-8956
- Volume :
- 4
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Nature medicine
- Publication Type :
- Academic Journal
- Accession number :
- 9427609
- Full Text :
- https://doi.org/10.1038/nm0198-072