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   <subfield code="a">In vitro antiplasmodial activity and cytotoxicity of crude extracts and compounds from the stem bark of Kigelia africana (Lam.) Benth (Bignoniaceae)</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Denis Zofou, Archile Kengne, Mathieu Tene, Moses Ngemenya, Pierre Tane, Vincent Titanji]</subfield>
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   <subfield code="a">In order to assess the potential of the stem bark of Kigelia africana (Lam.) Benth as source of new anti-malarial leads, n-hexane and ethyl acetate (EtOAc) extracts and four compounds isolated from the stem bark were screened in vitro against the chloroquine-resistant W-2 and two field isolates of Plasmodium falciparum using lactate dehydrogenase assay. The products were also tested for their cytotoxicity on LLC/MK2 monkey kidney cells. The EtOAc extract exhibited a significant antiplasmodial activity (IC50 = 11.15μg/mL on W-2; 3.91 and 4.74μg/mL on field CAM10 and SHF4 isolates, respectively), whereas the n-hexane fraction showed a weak activity (IC50 = 73.78μg/mL on W-2 and 21.85μg/mL on SHF4). Three out of the four compounds showed good activity against all the three different parasite strains (IC50 &lt; 5μM). Specicoside exhibited the highest activity on W-2 (IC50 = 1.54μM) followed by 2β, 3β, 19α-trihydroxy-urs-12-en-28-oic acid (IC50 = 1.60μM) and atranorin (IC50 = 4.41μM), while p-hydroxycinnamic acid was the least active (IC50 = 53.84μM). The EtOAc extract and its isolated compounds (specicoside and p-hydroxycinnamic acid) were non-cytotoxic (CC50 &gt; 30μg/mL), whereas the n-hexane extract and two of its products, atranorin and 2β, 3β, 19α-trihydroxy-urs-12-en-28-oic acid showed cytotoxicity at high concentrations, with the last one being the most toxic (CC50 = 9.37μg/mL). These findings justify the use of K. africana stem bark as antimalaria by traditional healers of Western Cameroon, and could constitute a good basis for further studies towards development of new leads or natural drugs for malaria.</subfield>
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