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A phenanthridin-6(5H)-one derivative and a lanostane-type triterpene with antibacterial properties from Anonidium mannii (Oliv). Engl. & Diels (Annonaceae).
Ngangoue, Marcelle Oliviane; Ngameni, Bathelemy; Ambassa, Pantaleon; Chi, Godloves Fru; Wamba, Brice Elvis Nougan; Ombito, Japheth Omollo; Bojase, Gomotsang Moleta; Fotso, Ghislain Wabo; Kuete, Victor; Ngadjui, Bonaventure Tchaleu.
Afiliación
  • Ngangoue MO; Faculty of Science, Department of Organic Chemistry, University of Yaoundé 1, Yaoundé, Cameroon.
  • Ngameni B; Faculty of Medicine and Biomedical Sciences, Department of Pharmacognosy and Pharmaceutical Chemistry, University of Yaoundé I, Yaoundé, Cameroon.
  • Ambassa P; Faculty of Science, Department of Organic Chemistry, University of Yaoundé 1, Yaoundé, Cameroon.
  • Chi GF; Faculty of Science, Department of Organic Chemistry, University of Yaoundé 1, Yaoundé, Cameroon.
  • Wamba BEN; Faculty of Science, Department of Biochemistry, University of Dschang, Dschang, Cameroon.
  • Ombito JO; Department of Chemistry, University of Botswana, Gaborone, Botswana.
  • Bojase GM; Department of Chemistry, University of Botswana, Gaborone, Botswana.
  • Fotso GW; Faculty of Science, Department of Organic Chemistry, University of Yaoundé 1, Yaoundé, Cameroon.
  • Kuete V; Faculty of Science, Department of Biochemistry, University of Dschang, Dschang, Cameroon.
  • Ngadjui BT; Faculty of Science, Department of Organic Chemistry, University of Yaoundé 1, Yaoundé, Cameroon.
Nat Prod Res ; 35(21): 4041-4050, 2021 Nov.
Article en En | MEDLINE | ID: mdl-32400185
ABSTRACT
The chemical investigation of Anonidium mannii root extract by column chromatography techniques led to the isolation of eight compounds among which two previously unreported compounds; a lanostane-type triterpene, lanosta-7,9(11),23-triene-3ß,15α-diol 1 and an alkaloid, 9-hydroxy-8-methoxyphenanthridin-6(5H)-one 2 along with six known compounds lanosta-7,9(11),24-triene-3ß,21-diol 3, oxoanolobine 4, 3, 4-dihydroxybenzoic acid 5, stigmasterol 6, ß-sitosterol 7 and 3-O-ß-D-glucopyranosyl-ß-stigmasterol 8. Their structures were established from spectral data, mainly HR-ESIMS, 1 D and 2 D NMR and by comparison with literature data. The crude root and stem bark extracts (AMR and AMB) and the isolated compounds (1-8) were tested against nine Gram-negative bacteria using rapid p-iodonitrotetrazolium chloride ≥97% (INT) microdilution technique. It was found that AMR, AMB and compound 5 were active against the nine tested bacteria with MIC values ranging from 64 to 1024 µg/mL. Compounds 1-4 had selective antibacterial activities whilst 6-8 were not active.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Triterpenos / Annonaceae Idioma: En Revista: Nat Prod Res Año: 2021 Tipo del documento: Article País de afiliación: Camerún

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Triterpenos / Annonaceae Idioma: En Revista: Nat Prod Res Año: 2021 Tipo del documento: Article País de afiliación: Camerún