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Literature DB >> 18234452

Anti-plasmodial activity of the extracts and two sesquiterpenes from Cyperus articulatus.

G M Rukunga¹, F W Muregi, S A Omar, J W Gathirwa, C N Muthaura, M G Peter, M Heydenreich, G M Mungai.

Abstract

Two sesquiterpenes, corymbolone and mustakone, isolated from the chloroform extract of the rhizomes of Cyperus articulatus, exhibited significant anti-plasmodial properties. Mustakone was approximately ten times more active than corymbolone against the sensitive strains of the Plasmodium falciparum.

Entities: Chemical Species

Mesh：

Substances：

Year: 2007 PMID： 18234452 DOI： 10.1016/j.fitote.2007.11.010

Source DB: PubMed Journal: Fitoterapia ISSN： 0367-326X Impact factor: 2.882

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Cited

7 in total

Review 1. Review on medicinal plants and natural compounds as anti-Onchocerca agents.

Authors: Dieudonné Ndjonka; Boursou Djafsia; Eva Liebau
Journal: Parasitol Res Date: 2018-07-15 Impact factor: 2.289

2. Anticonvulsant effect of ethanolic extract of Cyperus articulatus L. leaves on pentylenetetrazol induced seizure in mice.

Authors: Oscar Herrera-Calderon; Rocio Santiváñez-Acosta; Bertha Pari-Olarte; Edwin Enciso-Roca; Vicente Martin Campos Montes; Jorge Luis Arroyo Acevedo
Journal: J Tradit Complement Med Date: 2017-04-20

3. Cyperus articulatus L. (Cyperaceae) Rhizome Essential Oil Causes Cell Cycle Arrest in the G₂/M Phase and Cell Death in HepG2 Cells and Inhibits the Development of Tumors in a Xenograft Model.

Authors: Mateus L Nogueira; Emilly J S P de Lima; Asenate A X Adrião; Sheila S Fontes; Valdenizia R Silva; Luciano de S Santos; Milena B P Soares; Rosane B Dias; Clarissa A Gurgel Rocha; Emmanoel V Costa; Felipe M A da Silva; Marcos A Vannier-Santos; Nállarett M D Cardozo; Hector H F Koolen; Daniel P Bezerra
Journal: Molecules Date: 2020-06-09 Impact factor: 4.411

4. The in vitro and in vivo anti-hepatotoxic, anti-hepatitis B virus and hepatic CYP450 modulating potential of Cyperus rotundus.

Authors: Mohammad K Parvez; Mohammed S Al-Dosari; Ahmed H Arbab; Sakina Niyazi
Journal: Saudi Pharm J Date: 2019-02-05 Impact factor: 4.330

Anti-plasmodial activity of the extracts and two sesquiterpenes from Cyperus articulatus.

Review 1. Review on medicinal plants and natural compounds as anti-Onchocerca agents.

2. Anticonvulsant effect of ethanolic extract of Cyperus articulatus L. leaves on pentylenetetrazol induced seizure in mice.

3. Cyperus articulatus L. (Cyperaceae) Rhizome Essential Oil Causes Cell Cycle Arrest in the G₂/M Phase and Cell Death in HepG2 Cells and Inhibits the Development of Tumors in a Xenograft Model.

4. The in vitro and in vivo anti-hepatotoxic, anti-hepatitis B virus and hepatic CYP450 modulating potential of Cyperus rotundus.

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

6. Anti-Onchocerca activity and phytochemical analysis of an essential oil from Cyperus articulatus L.

7. Anti-onchocerca Metabolites from Cyperus articulatus: Isolation, In Vitro Activity and In Silico 'Drug-Likeness'.

Anti-plasmodial activity of the extracts and two sesquiterpenes from Cyperus articulatus.

Review 1. Review on medicinal plants and natural compounds as anti-Onchocerca agents.

2. Anticonvulsant effect of ethanolic extract of Cyperus articulatus L. leaves on pentylenetetrazol induced seizure in mice.

3. Cyperus articulatus L. (Cyperaceae) Rhizome Essential Oil Causes Cell Cycle Arrest in the G2/M Phase and Cell Death in HepG2 Cells and Inhibits the Development of Tumors in a Xenograft Model.

4. The in vitro and in vivo anti-hepatotoxic, anti-hepatitis B virus and hepatic CYP450 modulating potential of Cyperus rotundus.

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

6. Anti-Onchocerca activity and phytochemical analysis of an essential oil from Cyperus articulatus L.

7. Anti-onchocerca Metabolites from Cyperus articulatus: Isolation, In Vitro Activity and In Silico 'Drug-Likeness'.

3. Cyperus articulatus L. (Cyperaceae) Rhizome Essential Oil Causes Cell Cycle Arrest in the G₂/M Phase and Cell Death in HepG2 Cells and Inhibits the Development of Tumors in a Xenograft Model.