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Antiviral activity of constituents of Tamus communis.

Abstract
The antiviral activity of the phenanthrene derivatives 1-6, of the spyrostane triglycosides dioscin (7) and gracillin (8), of the furostanol tetraglycosides methylprotodioscin (9), its (25S) epimer methylprotoneodioscin (10), and methylprotogracillin 11, have been tested towards two RNA viruses: vesicular stomatitis virus and human rhinovirus type 1B. All these products were extracted from the rizomes of Tamus communis L; compound 11 was isolated also from Asparagus cochinchinesis, together with pseudoprotodioscin (12), a 20 (22)-unsaturated furostanoside, which was also investigated for antiviral activity. The results were of some interest mainly for the phenanthrene derivatives.
AuthorsR Aquino, C Conti, F De Simone, N Orsi, C Pizza, M L Stein
JournalJournal of chemotherapy (Florence, Italy) (J Chemother) Vol. 3 Issue 5 Pg. 305-9 (Oct 1991) ISSN: 1120-009X [Print] England
PMID1667189 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antiviral Agents
  • RNA, Viral
  • Spirostans
  • gracillin
  • dioscin
  • Diosgenin
Topics
  • Animals
  • Antiviral Agents (pharmacology)
  • Cell Division (drug effects)
  • Cells, Cultured
  • Diosgenin (analogs & derivatives, pharmacology)
  • HeLa Cells
  • Humans
  • Plants, Medicinal
  • RNA, Viral
  • Rhinovirus (drug effects, physiology)
  • Spirostans (pharmacology)
  • Vesicular stomatitis Indiana virus (drug effects, physiology)
  • Virus Replication (drug effects)

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