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AMD3100, a small molecule inhibitor of HIV-1 entry via the CXCR4 co-receptor.
Donzella, G A; Schols, D; Lin, S W; Esté, J A; Nagashima, K A; Maddon, P J; Allaway, G P; Sakmar, T P; Henson, G; De Clercq, E; Moore, J P.
  • Donzella GA; The Aaron Diamond AIDS Research Center, The Rockefeller University, New York, New York 10016, USA.
Nat Med ; 4(1): 72-7, 1998 Jan.
Article en En | MEDLINE | ID: mdl-9427609
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.
Asunto(s)
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Banco de datos: MEDLINE Asunto principal: Linfocitos T CD4-Positivos / VIH-1 / Fármacos Anti-VIH / Receptores CXCR4 / Quimiocinas CXC / Compuestos Heterocíclicos Límite: Humans Idioma: En Año: 1998 Tipo del documento: Article
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Banco de datos: MEDLINE Asunto principal: Linfocitos T CD4-Positivos / VIH-1 / Fármacos Anti-VIH / Receptores CXCR4 / Quimiocinas CXC / Compuestos Heterocíclicos Límite: Humans Idioma: En Año: 1998 Tipo del documento: Article