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Central neural tumor destruction by controlled release of a synthetic glycoside dispersed in a biodegradable polymeric matrix.

Abstract
An octyl N-acetylglucosaminide derivative with a pentaerythritol chain at position 6 has been synthesized and evaluated as an inhibitor of neural tumor growth. The glycoside inhibited the growth of a neuroectodermic tumor implanted in rats and, when loaded on a slow-delivery polymer disk, caused the destruction of cultured human astroblastoma obtained after surgical biopsy.
AuthorsAlfonso Fernández-Mayoralas, Natalia De La Figuera, Mercedes Zurita, Jesús Vaquero, Gustavo A Abraham, Julio San Román, Manuel Nieto-Sampedro
JournalJournal of medicinal chemistry (J Med Chem) Vol. 46 Issue 8 Pg. 1286-8 (Apr 10 2003) ISSN: 0022-2623 [Print] United States
PMID12672228 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • 2-acetamido-2-deoxy-6-O-(2,2-bis(hydroxymethyl)-3-hydroxypropyl)glucopyranoside
  • Antineoplastic Agents
  • Delayed-Action Preparations
  • Drug Carriers
  • Glycosides
  • Polymers
  • Propylene Glycols
  • Acetylglucosamine
Topics
  • Acetylglucosamine (analogs & derivatives, chemical synthesis, pharmacology)
  • Animals
  • Antineoplastic Agents (chemical synthesis, pharmacology)
  • Brain Neoplasms (chemically induced, drug therapy, pathology)
  • Delayed-Action Preparations
  • Drug Carriers
  • Female
  • Glycosides (chemical synthesis, pharmacology)
  • Humans
  • Male
  • Neoplasm Transplantation
  • Neoplasms, Neuroepithelial (pathology)
  • Neuroectodermal Tumors, Primitive (chemically induced, drug therapy, pathology)
  • Polymers
  • Propylene Glycols (chemical synthesis, pharmacology)
  • Rats
  • Rats, Wistar
  • Tumor Cells, Cultured

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