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Antiplasmodial prenylated flavanonols from Tephrosia subtriflora.
Muiva-Mutisya, Lois M; Atilaw, Yoseph; Heydenreich, Matthias; Koch, Andreas; Akala, Hoseah M; Cheruiyot, Agnes C; Brown, Matthew L; Irungu, Beatrice; Okalebo, Faith A; Derese, Solomon; Mutai, Charles; Yenesew, Abiy.
Afiliação
  • Muiva-Mutisya LM; a Department of Chemistry , University of Nairobi , Nairobi , Kenya.
  • Atilaw Y; a Department of Chemistry , University of Nairobi , Nairobi , Kenya.
  • Heydenreich M; b Institut für Chemie , Universität Potsdam , Potsdam , Germany.
  • Koch A; b Institut für Chemie , Universität Potsdam , Potsdam , Germany.
  • Akala HM; c United States Army Medical Research Directorate-Kenya (USAMRD-K), Kenya Medical Research Institute (KEMRI)/Walter Reed Project (WRP) , Kisumu , Kenya.
  • Cheruiyot AC; c United States Army Medical Research Directorate-Kenya (USAMRD-K), Kenya Medical Research Institute (KEMRI)/Walter Reed Project (WRP) , Kisumu , Kenya.
  • Brown ML; c United States Army Medical Research Directorate-Kenya (USAMRD-K), Kenya Medical Research Institute (KEMRI)/Walter Reed Project (WRP) , Kisumu , Kenya.
  • Irungu B; d Centre for Traditional Medicine and Drug Research , Kenya Medical Research Institute , Nairobi , Kenya.
  • Okalebo FA; e Department of Pharmacology and Pharmacognosy , University of Nairobi , Nairobi , Kenya.
  • Derese S; a Department of Chemistry , University of Nairobi , Nairobi , Kenya.
  • Mutai C; f Department of Medical Laboratory Sciences , Masinde Muliro University of Sciences and Technology , Kakamega , Kenya.
  • Yenesew A; a Department of Chemistry , University of Nairobi , Nairobi , Kenya.
Nat Prod Res ; 32(12): 1407-1414, 2018 Jun.
Article em En | MEDLINE | ID: mdl-28714338
ABSTRACT
The CH2Cl2/MeOH (11) extract of the aerial parts of Tephrosia subtriflora afforded a new flavanonol, named subtriflavanonol (1), along with the known flavanone spinoflavanone B, and the known flavanonols MS-II (2) and mundulinol. The structures were elucidated by the use of NMR spectroscopy and mass spectrometry. The absolute configuration of the flavanonols was determined based on quantum chemical ECD calculations. In the antiplasmodial assay, compound 2 showed the highest activity against chloroquine-sensitive Plasmodium falciparum reference clones (D6 and 3D7), artemisinin-sensitive isolate (F32-TEM) as well as field isolate (KSM 009) with IC50 values 1.4-4.6 µM without significant cytotoxicity against Vero and HEp2 cell lines (IC50 > 100 µM). The new compound (1) showed weak antiplasmodial activity, IC50 12.5-24.2 µM, but also showed selective anticancer activity against HEp2 cell line (CC50 16.9 µM).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Plasmodium falciparum / Flavonoides / Tephrosia / Antimaláricos Limite: Animals / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Plasmodium falciparum / Flavonoides / Tephrosia / Antimaláricos Limite: Animals / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article