Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 5 de 5
Filter
Add filters








Year range
1.
Rev. bras. farmacogn ; 29(6): 749-754, Nov.-Dec. 2019. tab, graf
Article in English | LILACS-Express | LILACS | ID: biblio-1057852

ABSTRACT

ABSTRACT This paper describes the chemical composition and the enantiomer content of the volatile oil hydrodistilled from Clinopodium brownei (Sw.) Kuntze, Lamiaceae. The plant was collected in the South of Ecuador. Thirty one components were identified by GC-MS, which accounted for the 96.15% of the volatile oil. The major components were pulegone (48.44%), menthone (34.55%) and β-acorenol (3.41%). Oxygenated monoterpenes (86.06%), followed by oxygenated sesquiterpenes (5.36%) constituted the most abundant fractions. The enantiomeric compositions of β-pinene, sabinene, 3-octanol, menthone, pulegone and menthyl acetate were determined by enantioselective GC-MS. (-)-Menthone showed the highest enantiomeric excess (ee = 83.4%). In in vitro tests, the volatile oil showed high selective inhibitory activity for butyrylcholinesterase with an IC50, 13.4 ± 1.8 µg/ml. In contrast, it was weakly active against acetylcholinesterase with an IC50 >250 µg/ml.

2.
Rev. bras. farmacogn ; 28(5): 559-563, Sept.-Oct. 2018. tab, graf
Article in English | LILACS | ID: biblio-977728

ABSTRACT

Abstract Lepechinia mutica (Benth.) Epling, Lamiaceae, and Vallea stipularis L.f., Elaeocarpaceae, are the object of the present study. These plants are endemic to the Andean region and have attracted our attention on the basis of interesting results obtained in a preliminary anticholinesterase screening. Actually, carnosol and tiliroside, isolated from L. mutica and V. stipularis, respectively, have shown a promising selective inhibitory activity against butyrylcholinesterase. Specifically, the anti-butyrylcholinesterase activity of carnosol was 5.15 µM and that of tiliroside was 52.9 µM, compared to 8.568 ± 0.570 µM of the positive control Donepezil. Carnosol and tiliroside were purified chromatographically from the ethyl acetate extract of L. mutica and V. stipularis, respectively. Spectrophotometric methods were used for enzymatic studies.

3.
Rev. bras. farmacogn ; 21(5): 850-855, Sept.-Oct. 2011. ilus, tab
Article in English | LILACS | ID: lil-600965

ABSTRACT

The essential oil of the species Clinopodium nubigenum (Kunth) Kuntze, Lamiaceae, was analyzed by GC-MS and GC-FID, taking into account the more recent literature. Among the seventy compounds identified, the majority are oxygenated monoterpenoids. The essential oil, tested for antimicrobial activity, resulted effective in vitro against Candida albicans. From the aqueous MeOH extract of the aerial parts of the plant two nonvolatile compounds, named schizonepetoside A and schizonepedoside C, have been isolated. They are rare glycosyl terpenoids, which were previously isolated from only one plant, but never found before in the genus Clinopodium.

4.
In. Naranjo, Plutarco; Escaleras, Ruperto. La medicina tradicional en el Ecuador - v.2. Quito, Universidad Andina Simón Bolivar, Corporación Editora Nacional, 1995. p.117-23, ilus, tab.
Monography in Spanish | LILACS | ID: lil-178449

ABSTRACT

El senecio canescens Humb., conocido vulgarmente como "orejas de conejo", es usado en la medicina popular para curar infecciones, dolores de cabeza y reumatismos. La investigación de las partes aéreas y de las raíces condujo a la determinación de compuestos furanoeremofilanos, entre los cuales se elució el primer furanoeremofilano hidroperóxido natural y dos nuevos derivados de la cacalohastina, uno de los cuales es un dimero. La fracción volatil fue analizada por GC-MS.


Subject(s)
Senecio , Furans/administration & dosage
5.
In. Naranjo, Plutarco; Escaleras, Ruperto. La medicina tradicional en el Ecuador - v.2. Quito, Universidad Andina Simón Bolivar, Corporación Editora Nacional, 1995. p.125-8.
Monography in Spanish | LILACS | ID: lil-178450
SELECTION OF CITATIONS
SEARCH DETAIL