Synthesis of an inhibitor of human immunodeficiency virus infection

Jpn J Cancer Res. 1989 Feb;80(2):95-8. doi: 10.1111/j.1349-7006.1989.tb02272.x.

Abstract

Anti-HIV effects of lentinan sulfate were investigated by using an HTLV-I-carrying cell line, MT-4, in vitro. Lentinan, a fungal branched (1----3)-beta-D-glucan, was sulfated to various degrees by means of two kinds of procedures using piperidine N-sulfonic acid in dimethyl sulfoxide or chlorosulfonic acid in pyridine. Lentinan sulfate with a sulfur content of more than 13.9% effectively prevented HIV-induced cytopathic effects (CPE) at concentrations of more than 3.3 micrograms/ml. However, low-substituted lentinan sulfate did not prevent HIV-induced CPE at any concentration tested. When the countercation was 50% Na+ and 50% pyridinium ion, the inhibitory capacity was low. Anticoagulant activity of the lentinan sulfate was also assessed.

MeSH terms

  • Anticoagulants
  • Antiviral Agents / chemical synthesis*
  • Antiviral Agents / pharmacology
  • Cell Division / drug effects
  • Cell Line
  • Cytopathogenic Effect, Viral / drug effects
  • Fluorescent Antibody Technique
  • HIV / drug effects*
  • HIV Antigens / biosynthesis
  • Human T-lymphotropic virus 1
  • Humans
  • Lentinan / analogs & derivatives
  • Lentinan / chemical synthesis*
  • Lentinan / pharmacology
  • Lentinan / therapeutic use
  • Polysaccharides / chemical synthesis*
  • Sulfur / metabolism

Substances

  • Anticoagulants
  • Antiviral Agents
  • HIV Antigens
  • Polysaccharides
  • lentinan sulfate
  • Lentinan
  • Sulfur