* Corresponding Author
Evaluation of the Antiplasmodial Properties of Andrographis paniculata (Burm.f.) and Peperomia pellucida (L.) Kunth
https://doi.org/10.22146/ijc.74481 Nurhayati Bialangi(1), Mohamad Adam Mustapa(2), Yuszda Salimi(3), Weny Musa(4), Ari Widiyantoro(5), Agus Malik Ibrahim(6), Boima Situmeang(7*), Julinton Sianturi(8)
(1) Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Gorontalo, Gorontalo 96128, Indonesia
(2) Department of Pharmacy, Faculty of Sport and Health Sciences, Universitas Negeri Gorontalo, Gorontalo 96128, Indonesia
(3) Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Gorontalo, Gorontalo 96128, Indonesia
(4) Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Gorontalo, Gorontalo 96128, Indonesia
(5) Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Tanjungpura, Pontianak 78115, Indonesia
(6) Department of Chemistry, Sekolah Tinggi Analis Kimia Cilegon, Banten, 42411, Indonesia
(7) Department of Chemistry, Sekolah Tinggi Analis Kimia Cilegon, Banten, 42411, Indonesia
(8) Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1, 14424 Potsdam, Germany
(*) Corresponding Author
Abstract
Plasmodium species are the infectious agents that are responsible for malaria, a disease that claims the lives of approximately 400,000 people annually. The fact that drug resistance against malaria is on the rise suggests that new antimalarial compounds need to be discovered. It is well known that medicinal plants present the best opportunity for the identification of novel antimalaria chemicals. Both the Andrographis paniculata (Burm.f.) and Peperomia pellucida (L. Kunth) species have been tested for their antiplasmodial ability against the Plasmodium falciparum strain. The P. pellucida (L. Kunth) species has also been subjected to in vitro and in vivo biological research. P. pellucida was used to isolate the steroid known as 3-hydroxy-24-ethyl-5,22-cholestadiene (1) and the triterpenoid known as 3-hydroxy-9-lanosta-7,24E-dien-26-oic acid (2). Both compounds were then tested for their activity in vitro. In the mice model, triterpenoid 2 had a substantial chemo-suppressive impact.
Keywords
References
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DOI: https://doi.org/10.22146/ijc.74481
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