The molecular target of bicyclams, potent inhibitors of human immunodeficiency virus replication.

Ítems similars

• Highly potent and selective inhibition of human immunodeficiency virus by the bicyclam derivative JM3100.
  per: De Clercq, E, et al.
  Publicat: (1994)
• Sensitivity of human immunodeficiency virus to bicyclam derivatives is influenced by the three-dimensional structure of gp120.
  per: De Vreese, K, et al.
  Publicat: (1997)
• Bicyclams, Selective Antagonists of the Human Chemokine Receptor CXCR4, Potently Inhibit Feline Immunodeficiency Virus Replication
  per: Egberink, Herman F., et al.
  Publicat: (1999)
• Potent and selective inhibition of human immunodeficiency virus (HIV)-1 and HIV-2 replication by a class of bicyclams interacting with a viral uncoating event.
  per: De Clercq, E, et al.
  Publicat: (1992)
• Antiviral efficacy in vivo of the anti-human immunodeficiency virus bicyclam SDZ SID 791 (JM 3100), an inhibitor of infectious cell entry.
  per: Datema, R, et al.
  Publicat: (1996)