| Literature DB >> 16442576 |
Kenneth Oben Eyong1, Gabriel Ngosong Folefoc, Victor Kuete, Veronique Penlap Beng, Karsten Krohn, Hidayat Hussain, Augustin Ephram Nkengfack, Michael Saeftel, Salem Ramadan Sarite, Achim Hoerauf.
Abstract
The study of the chemical constituents of the roots of Newbouldia laevis (Bignoniaceae) has resulted in the isolation and characterization of a naphthoquinone-anthraquinone coupled pigment named newbouldiaquinone A (1) together with 14 known compounds: apigenin, chrysoeriol, newbouldiaquinone, lapachol, 2-methylanthraquinone, 2-acetylfuro-1,4-naphthoquinone, 2,3-dimethoxy-1,4-benzoquinone, oleanolic acid, canthic acid, 2-(4-hydroxyphenyl)ethyl triacontanoate, newbouldiamide, 5,7-dihydroxydehydroiso-alpha-lapachone, beta-sitosterol, and beta-sitosterol glucopyranoside. The structure elucidation of the isolated compounds was established based on spectroscopic studies, notably of the 2D NMR spectra. The antimalarial activity of compound (1) against Plasmodium falciparum in vitro shows moderate chemo suppression of parasitic growth. Its antimicrobial activity against a wide range of microorganisms was 13- and 24-fold more active against Candida gabrata and Enterobacter aerogens than the reference antibiotics nystatin and gentamycin.Entities:
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Year: 2006 PMID: 16442576 DOI: 10.1016/j.phytochem.2005.12.019
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072