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Secondary metabolites of the leaves of Tricalysia atherura N. Hallé (Rubiaceae) and their potential antiplasmodial activity.
Djikam Sime, Gwladys; Mbabi Nyemeck, Norbert; Zintchem, Auguste Abouem A; October, Natasha; Missi, Marius Balemaken; Farooq, Rabia; Khan, Khalid Mohammed; Ngono Bikobo, Dominique Serge; Choudhary, Muhammad Iqbal; Pegnyemb, Dieudonné Emmanuel.
Afiliação
  • Djikam Sime G; Faculty of Science, Department of Organic Chemistry, University of Yaoundé 1, Yaoundé, Cameroon.
  • Mbabi Nyemeck N; International Center for Chemical and Biological Sciences, H.E.J Research Institute of Chemistry, University of Karachi, Karachi, Pakistan.
  • Zintchem AAA; Faculty of Science, Department of Organic Chemistry, University of Yaoundé 1, Yaoundé, Cameroon.
  • October N; Department of Chemistry, Faculty of Science, University of Dschang, Dschang, Cameroon.
  • Missi MB; Faculty of Science, Department of Organic Chemistry, University of Yaoundé 1, Yaoundé, Cameroon.
  • Farooq R; Department of Chemistry, Higher Teacher's Training College, University of Yaoundé 1, Yaoundé, Cameroon.
  • Khan KM; Department of Chemistry, University of Pretoria, Hatfield, South Africa.
  • Ngono Bikobo DS; Faculty of Science, Department of Organic Chemistry, University of Yaoundé 1, Yaoundé, Cameroon.
  • Choudhary MI; Department of Chemistry, University of Pretoria, Hatfield, South Africa.
  • Pegnyemb DE; International Center for Chemical and Biological Sciences, H.E.J Research Institute of Chemistry, University of Karachi, Karachi, Pakistan.
Nat Prod Res ; 37(17): 2830-2840, 2023.
Article em En | MEDLINE | ID: mdl-36282891
One monoterpene indole alkaloid, atheruramine (1) bearing an ether bridge linking, one hydrobenzoin derivative, tricalydioloside (2) and two ursane-type triterpenes, atherurosides (A and B) (3 and 4) were isolated from the leaves of Tricalysia atherura, together with eight known compounds. The structures of these new compounds were elucidated on the basis of the results of spectroscopic analysis, and the relative configurations of compounds 1-3 were established by NOE difference. Four of the metabolites were screened in vitro against both chloroquine (CQ)-sensitive (3D7) and -resistant (Dd2) strains of Plasmodium falciparum; they were found to exhibit moderate activity against chloroquine-resistant (Dd2) (IC50 64.99-92.29 µg/mL). Meanwhile, crude extract possesses high antiplasmodial activity against both 3D7 and Dd2 strains of P. falciparum (IC50 4.39-7.54 µg/mL) and high selectivity indices values (SI > 10) and was found to be safe.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article