Sylvestre Saidou Tsila , Claire Christine Waleguele , Noella Molisa Efange , Billy Toussie Tchegnitegni , Jean Rodolphe Chouna , Angelbert Fusi Awantu , Yannick Stéphane Fotsing Fongang , Lawrence Ayong , Norbert Sewald , Bruno Ndjakou Lenta
{"title":"Antiplasmodial-guided isolation of constituents from the stem bark of Balanites aegyptiaca","authors":"Sylvestre Saidou Tsila , Claire Christine Waleguele , Noella Molisa Efange , Billy Toussie Tchegnitegni , Jean Rodolphe Chouna , Angelbert Fusi Awantu , Yannick Stéphane Fotsing Fongang , Lawrence Ayong , Norbert Sewald , Bruno Ndjakou Lenta","doi":"10.1016/j.phytol.2025.02.016","DOIUrl":null,"url":null,"abstract":"<div><div>The CH<sub>2</sub>Cl<sub>2</sub>/MeOH (1:1, v/v) extract of the stem bark of <em>Balanites aegyptiaca</em> showed moderate antiplasmodial activity against both the chloroquine sensitive <em>Plasmodium falciparum</em> 3D7 (<em>Pf</em>3D7) and multidrug-resistant <em>Plasmodium falciparum</em> Dd2 (<em>Pf</em>Dd2) strains with IC<sub>50</sub> values of 14.20 ± 1.92 and 42.14 ± 2.83 <em>µ</em>g/mL, respectively. The extract was successively subjected to liquid-liquid partition with <em>n-</em>hexane, ethyl acetate, and <em>n-</em>butanol, and the fractions obtained were assessed for their antiplasmodial activity against the same strains. The ethyl acetate soluble fraction was the most active one with IC<sub>50</sub> values of 7.74 ± 0.74 and 19.27 ± 2.15 <em>µ</em>g/mL against <em>Pf</em>3D7 and <em>Pf</em>Dd2, respectively, followed by the <em>n-</em>hexane fraction (IC<sub>50</sub> = values of 31.06 ± 2.60 and 90.67 ± 0.07 <em>µ</em>g/mL against <em>Pf</em>3D7 and <em>Pf</em>Dd2, respectively). The <em>n-</em>butanol fraction was inactive (IC<sub>50</sub> > 50 <em>µ</em>g/mL). Successive column chromatography of the active fractions led to the isolation of fifteen compounds including two new lignans [balanitals A (<strong>1</strong>) and B (<strong>2</strong>)], together with 13 known compounds (<strong>3</strong>–<strong>15</strong>). Their structures were established by means of spectroscopic methods. The isolated compounds were also assessed for their antiplasmodial activity against both <em>Pf</em>3D7 and <em>Pf</em>Dd2. Compound <strong>4</strong> exhibited a good antiplasmodial activity with an IC<sub>50</sub> value of 4.95 ± 0.70 <em>µ</em>M against <em>Pf</em>3D7, while it was not active against <em>Pf</em>Dd2 (IC<sub>50</sub> > 100 <em>µ</em>M).</div></div>","PeriodicalId":20408,"journal":{"name":"Phytochemistry Letters","volume":"66 ","pages":"Pages 126-130"},"PeriodicalIF":1.3000,"publicationDate":"2025-03-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytochemistry Letters","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1874390025010286","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0
Abstract
The CH2Cl2/MeOH (1:1, v/v) extract of the stem bark of Balanites aegyptiaca showed moderate antiplasmodial activity against both the chloroquine sensitive Plasmodium falciparum 3D7 (Pf3D7) and multidrug-resistant Plasmodium falciparum Dd2 (PfDd2) strains with IC50 values of 14.20 ± 1.92 and 42.14 ± 2.83 µg/mL, respectively. The extract was successively subjected to liquid-liquid partition with n-hexane, ethyl acetate, and n-butanol, and the fractions obtained were assessed for their antiplasmodial activity against the same strains. The ethyl acetate soluble fraction was the most active one with IC50 values of 7.74 ± 0.74 and 19.27 ± 2.15 µg/mL against Pf3D7 and PfDd2, respectively, followed by the n-hexane fraction (IC50 = values of 31.06 ± 2.60 and 90.67 ± 0.07 µg/mL against Pf3D7 and PfDd2, respectively). The n-butanol fraction was inactive (IC50 > 50 µg/mL). Successive column chromatography of the active fractions led to the isolation of fifteen compounds including two new lignans [balanitals A (1) and B (2)], together with 13 known compounds (3–15). Their structures were established by means of spectroscopic methods. The isolated compounds were also assessed for their antiplasmodial activity against both Pf3D7 and PfDd2. Compound 4 exhibited a good antiplasmodial activity with an IC50 value of 4.95 ± 0.70 µM against Pf3D7, while it was not active against PfDd2 (IC50 > 100 µM).
期刊介绍:
Phytochemistry Letters invites rapid communications on all aspects of natural product research including:
• Structural elucidation of natural products
• Analytical evaluation of herbal medicines
• Clinical efficacy, safety and pharmacovigilance of herbal medicines
• Natural product biosynthesis
• Natural product synthesis and chemical modification
• Natural product metabolism
• Chemical ecology
• Biotechnology
• Bioassay-guided isolation
• Pharmacognosy
• Pharmacology of natural products
• Metabolomics
• Ethnobotany and traditional usage
• Genetics of natural products
Manuscripts that detail the isolation of just one new compound are not substantial enough to be sent out of review and are out of scope. Furthermore, where pharmacology has been performed on one new compound to increase the amount of novel data, the pharmacology must be substantial and/or related to the medicinal use of the producing organism.