2008
DOI: 10.1016/j.jep.2007.12.017
|View full text |Cite
|
Sign up to set email alerts
|

Antimicrobial activity of the crude extracts and five flavonoids from the twigs of Dorstenia barteri (Moraceae)

Abstract: The aim of this study was to evaluate the antimicrobial activity of the crude extract of the twigs of Dorstenia barteri (DBT) as well as that of four of the five flavonoids isolated from this extract. Gram-positive bacteria (six species), Gram-negative bacteria (12 species) and fungi (four species) were used. The agar disc diffusion test was used to determine the sensitivity of the tested samples while the well micro-dilution was used to determine the minimal inhibition concentrations (MIC) and the minimal mic… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
86
0
2

Year Published

2009
2009
2024
2024

Publication Types

Select...
8
1

Relationship

2
7

Authors

Journals

citations
Cited by 148 publications
(89 citation statements)
references
References 15 publications
1
86
0
2
Order By: Relevance
“…The procedure was repeated using plant extracts at 1.0 g/ml in place of SIRE. The general antimicrobial activity using Escherichia coli (ATCC 2592), Staphylococcus aureus (ATCC 25923) and Candida albican (ATCC 90028) was assayed by standard disc diffusion method according to Ayo et al (2007), Mbaveng et al (2008), Ngoci et al (2012) and Mwitari et al (2013).…”
Section: Antitubercular and Antimicrobial Activity Screeningmentioning
confidence: 99%
“…The procedure was repeated using plant extracts at 1.0 g/ml in place of SIRE. The general antimicrobial activity using Escherichia coli (ATCC 2592), Staphylococcus aureus (ATCC 25923) and Candida albican (ATCC 90028) was assayed by standard disc diffusion method according to Ayo et al (2007), Mbaveng et al (2008), Ngoci et al (2012) and Mwitari et al (2013).…”
Section: Antitubercular and Antimicrobial Activity Screeningmentioning
confidence: 99%
“…1) were obtained from the chemical bank of the Laboratory of Organic Chemistry, University of Yaoundé I, Cameroon. Isolation and identification of the following compounds have been reported previously [10][11][12][13]: crotozambefurans A, B and C; bartericin C; MAB3; mammeisin; norcassaide; norerythrosuaveolide; 1,8-dihydroxy-6-methoxy-3-methylanthraquinone; 3-geranyloxy-6-methyl-1,8-dihydroxyanthraquinone; vismiaquinone and vismiaquinone C; bivismiaquinone; laurentixanthone B; kaempferol; lapachol; 2-acetylfuro-1,4-naphathoquinone; newbouldiaquinone and newbouldiaquinone A; hardwickiic acid; 3-friedelanone; betulinic acid; oleanolic acid; 7-methoxycoumarin; 7-hydroxycoumarin; 1,5-dihydroxyxanthone; smeathxanthone A and smeathxanthone B; gancaonin Q; stipulin; angusticornin B; 1,7-dihydroxyxanthone; 4-hydroxylonchocarpin; and quercetin.…”
Section: Chemicals For Antimicrobial Assaysmentioning
confidence: 99%
“…Their identification was confirmed before use at the Laboratory of Applied Microbiology and Molecular Pharmacology (LMP) (Faculty of Science, University of Yaoundé I). This was followed by culturing on the specific media and biochemical test using the API system (Mbaveng et al, 2008b).…”
Section: Microbial Strainsmentioning
confidence: 99%