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Research article summary (published 30 Jan 2006):

New macrocyclic lathyrane diterpenes, from Euphorbia lagascae, as inhibitors of multidrug resistance of tumour cells.

Full Abstract

The new macrocyclic lathyrane diterpenes latilagascenes A and B ( 1 and 2), the diacetylated derivative of 2, latilagascene C ( 3), and the known diterpenes ent-16alpha,17-dihydroxyatisan-3-one ( 4) and ent-16alpha,17-dihydroxykauran-3-one ( 5), isolated from the methanol extract of Euphorbia lagascae, were examined for their effects on the reversal of multidrug resistance (MDR) on mouse lymphoma cells. Among the active lathyrane derivatives 1 - 3, compound 2 displayed the highest inhibition of rhodamine 123 efflux of human MDR1 gene transfected mouse lymphoma cells when compared to the untreated cells or the positive control verapamil. The new compounds are the first macrocyclic lathyrane diterpenes showing oxidation at C-16, whose structures were characterized by extensive spectroscopic methods, including 2D NMR experiments ( (1)H- (1)H COSY, HMQC, HMBC and NOESY). The known phenolic compounds vanillic acid ( 6), p-salicylic acid ( 7), isofraxidin ( 8) and cleomiscosin A ( 9) were also isolated from this species.

 

Author information

Author/s: Duarte, Noélia (N); Gyémánt, Nora (N); Abreu, Pedro M (PM); Molnár, Joseph (J); Ferreira, Maria-José U (MJ);

Affiliation: CECF, Faculty of Pharmacy, University of Lisbon, Av. das Forças Armadas, 1600-083 Lisbon, Portugal.

Journal and publication information

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal: Planta medica (Planta Med), published in Germany. (Language: eng)

Reference: 2006-Feb; vol 72 (issue 2) : pp 162-8

Dates: Created 2006/02/21; Completed 2006/04/19; Revised 2006/11/15;

PMID: 16491453, status: MEDLINE (last retrieval date: 2/18/2009, IMS Date: )

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

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MeSH headings (categories)

This article was linked to the MESH Headings shown below.

Associated Chemicals: Antineoplastic Agents, Phytogenic (0) ; Diterpenes (0) ; Plant Extracts (0)

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