Literature DB >> 16168652

New clerodane diterpenoids from Laetia procera (Poepp.) Eichler (Flacourtiaceae), with antiplasmodial and antileishmanial activities.

Valérie Jullian1, Colin Bonduelle, Alexis Valentin, Lucia Acebey, Anne-Gaëlle Duigou, Marie-Francoise Prévost, Michel Sauvain.   

Abstract

Extracts of Laetia procera (Flacourtiaceae) displayed significant in vitro activity against Plasmodium falciparum. P. falciparum bioassay guided fractionation of a trunk bark extract of this plant led to the isolation of six clerodane diterpenoids (1-6) and a butanolide (7). Five of these compounds are new and called Laetiaprocerine A-D (3-6) and Laetianolide A (7). Their structures were established on the basis of 1D and 2D NMR experiments. Absolute configurations of 1 and 2 were determined by a modified Mosher's method and the absolute configuration of 5 by chemical correlation. The clerodane diterpenoids displayed activities against P. falciparum with an IC50 down to 0.5 microM on FCb1 and F32 strains, and also cytotoxicity toward human tumor cell line MCF7. The most active compound showed a selectivity index of 6.8. Some of these compounds also displayed activities against Leishmania amazonensis amastigote axenic stages and promastigote.

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Year:  2005        PMID: 16168652     DOI: 10.1016/j.bmcl.2005.07.090

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  6 in total

Review 1.  Clerodane diterpenes: sources, structures, and biological activities.

Authors:  Rongtao Li; Susan L Morris-Natschke; Kuo-Hsiung Lee
Journal:  Nat Prod Rep       Date:  2016-07-18       Impact factor: 13.423

2.  Corymbulosins I-W, Cytotoxic Clerodane Diterpenes from the Bark of Laetia corymbulosa.

Authors:  Simayijiang Aimaiti; Airi Suzuki; Yohei Saito; Shuichi Fukuyoshi; Masuo Goto; Katsunori Miyake; David J Newman; Barry R O'Keefe; Kuo-Hsiung Lee; Kyoko Nakagawa-Goto
Journal:  J Org Chem       Date:  2018-01-10       Impact factor: 4.354

3.  Corymbulosins D-H, 2-Hydroxy- and 2-Oxo-clerodane Diterpenes from the Bark of Laetia corymbulosa.

Authors:  Airi Suzuki; Yohei Saito; Shuichi Fukuyoshi; Masuo Goto; Katsunori Miyake; David J Newman; Barry R O'Keefe; Kuo-Hsiung Lee; Kyoko Nakagawa-Goto
Journal:  J Nat Prod       Date:  2017-03-14       Impact factor: 4.050

4.  Cytotoxic clerodane diterpenoids and their hydrolysis products from Casearia nigrescens from the rainforest of Madagascar.

Authors:  Russell B Williams; Andrew Norris; James S Miller; Chris Birkinshaw; Fidy Ratovoson; Rabodo Andriantsiferana; Vincent E Rasamison; David G I Kingston
Journal:  J Nat Prod       Date:  2007-02       Impact factor: 4.050

5.  Clerodane diterpenes from Casearia arguta that act as synergistic TRAIL sensitizers.

Authors:  Emily L Whitson; Cheryl L Thomas; Curtis J Henrich; Thomas J Sayers; James B McMahon; Tawnya C McKee
Journal:  J Nat Prod       Date:  2010-11-10       Impact factor: 4.050

6.  In vitro antimalarial activity of different extracts of Eremostachys macrophylla Montbr. & Auch.

Authors:  Solmaz Asnaashari; Fariba Heshmati Afshar; Atefeh Ebrahimi; Sedigheh Bamdad Moghadam; Abbas Delazar
Journal:  Bioimpacts       Date:  2015-08-19
  6 in total

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