Literature DB >> 20189612

Antiplasmodial activity of (I-3,II-3)-biflavonoids and other constituents from Ormocarpum kirkii.

Liene Dhooghe1, Sheila Maregesi, Irena Mincheva, Daneel Ferreira, Jannie P J Marais, Filip Lemière, An Matheeussen, Paul Cos, Louis Maes, Arnold Vlietinck, Sandra Apers, Luc Pieters.   

Abstract

Preliminary screening of a series of medicinal plants, traditionally used in Tanzania, showed an IC(50) of 15.6-31.2 microg/ml for the crude extract of the root of Ormocarpum kirkii S. Moore (Papilionaceae) against Plasmodium falciparum. A bioguided isolation was performed in order to isolate the active constituents. Twelve constituents were obtained and identified using NMR and MS data, and optical rotation measurements. The compounds comprised seven (I-3,II-3)-biflavonoids, three (I-3,II-3)-bi-4-phenyldihydrocoumarins, an isoflavanone and a C-glucosylated flavone. Six compounds, liquiritigeninyl-(I-3,II-3)-naringenin, apigeninyl-(I-3,II-3)-naringenin, 7-O-beta-D-glucopyranosylchamaejasmin, (3R,4S,3''R,4''S)-5,5''-di-O-methyldiphysin, 7-O-beta-D-glucopyranosyldiphysin, and 4''-hydroxydiphysolone, were isolated in addition to six known components. The compounds were evaluated for antimicrobial activity in a broad screening panel, including P. falciparum. Seven of these showed antiplasmodial activity; isochamaejasmin being the most active with an IC(50) of 7.3+/-3.8 microM, but the selectivity was rather limited. Thus, these constituents may contribute, at least in part, to the antimalarial use of O. kirkii in traditional medicine. Copyright 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20189612     DOI: 10.1016/j.phytochem.2010.02.005

Source DB:  PubMed          Journal:  Phytochemistry        ISSN: 0031-9422            Impact factor:   4.072


  8 in total

1.  Antiplasmodial activity of some phenolic compounds from Cameroonians Allanblackia.

Authors:  Anatole Guy Blaise Azebaze; Jean Emmanuel Mbosso Teinkela; Edwige Laure Nguemfo; Alexis Valentin; Alain Bertrand Dongmo; Juliette Catherine Vardamides
Journal:  Afr Health Sci       Date:  2015-09       Impact factor: 0.927

Review 2.  Circular dichroism calculation for natural products.

Authors:  Alfarius Eko Nugroho; Hiroshi Morita
Journal:  J Nat Med       Date:  2013-04-07       Impact factor: 2.343

3.  In vitro antiplasmodial activity of crude extracts of Tetrapleura tetraptera and Copaifera religiosa.

Authors:  Jean Bernard Lekana-Douki; Sandrine Lydie Oyegue Liabagui; Jean Bernard Bongui; Rafika Zatra; Jacques Lebibi; Fousseyni S Toure-Ndouo
Journal:  BMC Res Notes       Date:  2011-11-23

4.  Naturally Occurring Cytotoxic [3'→8″]-Biflavonoids from Podocarpus nakaii.

Authors:  Pen-Ho Yeh; Yun-Dar Shieh; Li-Chun Hsu; Li-Ming Yang Kuo; Jhih-Hu Lin; Chia-Ching Liaw; Yao-Haur Kuo
Journal:  J Tradit Complement Med       Date:  2012-07

5.  Biflavanones, Chalconoids, and Flavonoid Analogues from the Stem Bark of Ochna holstii.

Authors:  Thobias M Kalenga; Monica M Ndoile; Yoseph Atilaw; Pieter J Gilissen; Joan J E Munissi; Anastasia Rudenko; Catarina Bourgard; Per Sunnerhagen; Stephen S Nyandoro; Mate Erdelyi
Journal:  J Nat Prod       Date:  2021-01-29       Impact factor: 4.050

6.  Ethnobotanical study of plants used by the traditional healers to treat malaria in Mogovolas district, northern Mozambique.

Authors:  Leonardo Manuel; Aurélio Bechel; Emília Virgínia Noormahomed; Delfina Fernandes Hlashwayo; Maria do Céu Madureira
Journal:  Heliyon       Date:  2020-12-18

7.  In Vitro and In Silico Potential Inhibitory Effects of New Biflavonoids from Ochna rhizomatosa on HIV-1 Integrase and Plasmodium falciparum.

Authors:  Angélique Nicolas Messi; Susan Lucia Bonnet; Brice Ayissi Owona; Anke Wilhelm; Eutrophe Le Doux Kamto; Joseph Thierry Ndongo; Xavier Siwe-Noundou; Madan Poka; Patrick H Demana; Rui W M Krause; Joséphine Ngo Mbing; Dieudonné Emmanuel Pegnyemb; Christian G Bochet
Journal:  Pharmaceutics       Date:  2022-08-15       Impact factor: 6.525

8.  Total synthesis of ochnaflavone.

Authors:  Monica M Ndoile; Fanie R van Heerden
Journal:  Beilstein J Org Chem       Date:  2013-07-08       Impact factor: 2.883

  8 in total

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