| Literature DB >> 16499336 |
Emmanoel V Costa1, Maria Lúcia B Pinheiro, Clahildek M Xavier, Jefferson R A Silva, Ana Cláudia F Amaral, Afonso D L Souza, Andersson Barison, Francinete R Campos, Antonio G Ferreira, Gérzia M C Machado, Leonor L P Leon.
Abstract
Bioassay-guided fractionation of the bark extract of Annona foetida afforded a new antileishmanial pyrimidine-beta-carboline alkaloid, N-hydroxyannomontine (1), together with the previously reported annomontine (2), O-methylmoschatoline (3), and liriodenine (4). The structure of compound 1 was established on the basis of extensive 1D and 2D NMR and MS analyses. This is the third reported pyrimidine-beta-carboline-type alkaloid and is particularly important for Annona genus chemotaxonomy. In addition, all compounds exhibit in vitro antileishmanial activity against promastigote forms of Leishmania braziliensis. Compounds 2 and 4 showed better activity than compounds 1 and 3 against L. braziliensis. Compound 2 was not active against L. guyanensis.Entities:
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Year: 2006 PMID: 16499336 DOI: 10.1021/np050422s
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050