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Jatrophane diterpenoids from Euphorbia mongolica as modulators of the multidrug resistance of L5128 mouse lymphoma cells.

Abstract
The dried aerial parts of Euphorbia mongolica afforded three new acylated polyhydroxy diterpenoids based on the jatrophane framework. The structures were established by means of a combination of 1D and 2D NMR techniques and mass spectrometry as (2S,3S,4R,5R,7S,8R,13S,15R)-5alpha,7beta,8alpha-triacetoxy-3beta-benzoyloxy-15beta-hydroxyjatropha-6(17),11E-diene-9,14-dione (1), (2S,3S,4R,5R,7S,8S,9S13S,15R)-5alpha,7beta,8alpha,9alpha,15beta-pentaacetoxy-3beta-benzoyloxyjatropha-6(17),11E-dien-14-one (2), and (2S,3S,4R,5R,7S,8S,9S13S,15R)-3beta,7beta,8alpha,9alpha,15beta-pentaacetoxy-5alpha-benzoyloxyjatropha-6(17),11E-dien-14-one (3). When the isolates were assayed for multidrug resistance-reversing activity in a rhodamine 123 exclusion test using L5178 mouse lymphoma cells, all compounds demonstrated a concentration-dependent effect in inhibiting the efflux pump activity of these tumor cells in the range 11.2-112 microM.
AuthorsJudit Hohmann, Dóra Rédei, Peter Forgo, József Molnár, György Dombi, Tomur Zorig
JournalJournal of natural products (J Nat Prod) Vol. 66 Issue 7 Pg. 976-9 (Jul 2003) ISSN: 0163-3864 [Print] United States
PMID12880317 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents, Phytogenic
  • Diterpenes
Topics
  • Animals
  • Antineoplastic Agents, Phytogenic (chemistry, isolation & purification, pharmacology)
  • Diterpenes (chemistry, isolation & purification, pharmacology)
  • Drug Resistance, Multiple (drug effects)
  • Drug Screening Assays, Antitumor
  • Euphorbia (chemistry)
  • Lymphoma
  • Mice
  • Molecular Structure
  • Mongolia
  • Nuclear Magnetic Resonance, Biomolecular
  • Plants, Medicinal (chemistry)
  • Stereoisomerism
  • Tumor Cells, Cultured (drug effects)

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