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Polysaccharides from Sargassum tenerrimum: structural features, chemical modification and anti-viral activity.

Abstract
Herpes simplex viruses (HSVs) display affinity for cell-surface heparan sulfate proteoglycans with biological relevance in virus entry. Here, we exploit an approach to inhibiting HSV infection by using a sulfated fucoidan, and a guluronic acid-rich alginate derived from Sargassum tenerrimum, mimicking the active domain of the entry receptor. These macromolecules have apparent molecular masses of 30+/-5 and 26+/-5 kDa, respectively. They and their chemically sulfated derivatives showed activity against herpes simplex virus type 1 (HSV-1). Their inhibitory concentration 50% (IC(50)) values were in the range 0.5-15 microg/ml and they lacked cytotoxicity at concentrations up to 1000 microg/ml. The anti-HSV activity increased with increasing sulfate ester content. Our results suggest the feasibility of inhibiting HSV infection by blocking viral entry with polysaccharide having specific structure.
AuthorsSharmistha Sinha, Akram Astani, Tuhin Ghosh, Paul Schnitzler, Bimalendu Ray
JournalPhytochemistry (Phytochemistry) Vol. 71 Issue 2-3 Pg. 235-42 (Feb 2010) ISSN: 1873-3700 [Electronic] England
PMID19931103 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright2009 Elsevier Ltd. All rights reserved.
Chemical References
  • Alginates
  • Antiviral Agents
  • Hexuronic Acids
  • Plant Extracts
  • Polysaccharides
  • guluronic acid
  • Glucuronic Acid
  • fucoidan
Topics
  • Alginates (chemistry, pharmacology, therapeutic use)
  • Animals
  • Antiviral Agents (chemistry, pharmacology, therapeutic use)
  • Cells, Cultured
  • Glucuronic Acid (chemistry, pharmacology, therapeutic use)
  • Haplorhini
  • Herpes Simplex (drug therapy, virology)
  • Herpesvirus 1, Human (drug effects)
  • Hexuronic Acids (chemistry, pharmacology, therapeutic use)
  • Inhibitory Concentration 50
  • Phytotherapy
  • Plant Extracts (chemistry, pharmacology, therapeutic use)
  • Polysaccharides (chemistry, pharmacology, therapeutic use)
  • Sargassum (chemistry)
  • Structure-Activity Relationship
  • Virus Integration (drug effects)

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