scholarly journals Composition and Chemical Variability of Root Bark oil from Ivoirian Cleistopholis patens

2018 ◽  
Vol 13 (6) ◽  
pp. 1934578X1801300
Author(s):  
Zana A. Ouattara ◽  
Thierry A. Yapi ◽  
Yves-Alain Békro ◽  
Akhanovna J. Mamyrbékova-Békro ◽  
Mathieu Paoli ◽  
...  

The chemical composition of root bark oil of Cleistopholis patens (Benth.) Engl. & Diels from Côte d'Ivoire was determined by GC (in combination with retention indices), GC-MS and 13C NMR. The contents of the major compounds varied drastically from sample to sample: patchoulenone (0–70.5%), β-pinene (0–51.9%), bornyl acetate (0.5–31.2%), α-pinene (0.2–25.7%), juvenile hormone III (0.3–22.2%) and β-elemol (0–18.8%). Three chemical compositions may be differentiated, dominated by i) patchoulenone, ii) β-pinene and α-pinene, iii) juvenile hormone III, accompanied by bornyl acetate or β-elemol. 13C NMR data of patchoulenol (3-patchoulen-5- exo-ol) are reported.

2015 ◽  
Vol 10 (6) ◽  
pp. 1934578X1501000
Author(s):  
Thierry Acafou Yapi ◽  
Jean Brice Boti ◽  
Antoine Coffy Ahibo ◽  
Sylvain Sutour ◽  
Ange Bighelli ◽  
...  

The chemical composition of a leaf oil sample from Ivoirian Xylopia staudtii Engler & Diels (Annonaceae) has been investigated by a combination of chromatographic [GC(RI)] and spectroscopic (GC-MS, 13C NMR) techniques. Thirty-five components that accounted for 91.8% of the whole composition have been identified. The oil composition was dominated by the furanoguaiadienes furanoguaia-1,4-diene (39.0%) and furanoguaia-1,3-diene (7.5%), and by germacrene D (17.5%). The composition of twelve other leaf oil samples demonstrated qualitative homogeneity, but quantitative variability. Indeed, the contents of the major components varied substantially: furanoguaia-1,4-diene (24.7–51.7%) and germacrene D (5.9–24.8%). The composition of X. staudtii leaf oil is close to that of X. rubescens leaf oil but varied drastically from those of the essential oils isolated from other Xylopia species. 13C NMR spectroscopy appeared as a powerful and complementary tool for analysis of sesquiterpene-rich essential oils.


Molecules ◽  
2019 ◽  
Vol 24 (14) ◽  
pp. 2575 ◽  
Author(s):  
Medbouhi ◽  
Benbelaïd ◽  
Djabou ◽  
Beaufay ◽  
Bendahou ◽  
...  

The chemical composition of essential oils extracted from aerial parts of Eryngium campestre collected in 37 localities from Western Algeria was characterized using GC-FID and GC/MS analyses. Altogether, 52 components, which accounted for 70.1 to 86.8% of the total composition oils were identified. The main compounds were Germacrene D (0.4–53.4%), Campestrolide (1.6–35.3%), Germacrene B (0.2–21.5%), Myrcene (0.1–8.4%), α-Cadinol (0.2–7.6%), Spathulenol (0.1–7.6%), Eudesma-4(15)-7-dien-1-β-ol (0.1–7.6%) and τ-Cadinol (0.3–5.5%). The chemical compositions of essential oils obtained from separate organs and during the complete vegetative cycle of the plant were also studied. With the uncommon 17-membered ring lactone named Campestrolide as the main component, Algerian E. campestre essential oils exhibited a remarkable chemical composition. A study of the chemical variability using statistical analysis allowed the discrimination of two main clusters according to the geographical position of samples. The study contributes to the better understanding of the relationship between the plant and its environment. Moreover, the antimicrobial activity of the essential oil was assessed against twelve strains bacteria and two yeasts involved in foodborne and nosocomial infections using paper disc diffusion and dilution agar assays. The in vitro study demonstrated a strong activity against Gram-positive strains such as S. aureus, B. cereus, and E. faecalis. The cytotoxicity and antiparasitic activities (on Lmm and Tbb) of the collective essential oil and one sample rich in campestrolide, as well as some enriched fractions or fractions containing other terpenic compounds, were also analyzed. Campestrolide seems to be one compound responsible for the cytotoxic and antileishmanial effect, while myrcene or/and trans-β-farnesene have a more selective antitrypanosomal activity.


2018 ◽  
Vol 13 (8) ◽  
pp. 1934578X1801300
Author(s):  
Joséphine Ottavioli ◽  
Ange Bighelli ◽  
Joseph Casanova ◽  
Félix Tomi

Juniperus communis L. var. communis is widespread in European countries. In Corsica a very small population grows wild in the North-Eastern side of the island. The chemical compositions of nine needle oil samples and three berry oil samples from Corsican J. communis L. var. communis have been investigated by GC(RI), GC-MS and 13C NMR. The composition of needle oils was dominated by monoterpene hydrocarbons, α-pinene (2/9 oil samples, 70.4 and 67.1%) or sabinene (7/9 oil samples, 24.4–45.3%). Berry oils displayed α-pinene/myrcene (43.0/24.1%) or α-pinene/sabinene/limonene/terpinen-4-ol (19.9/17.3/14.0/13.8%) as main components. A third oil sample contained mainly α-pinene (22.0%) accompanied by 21 sesquiterpenes (42.0% in total). It is noticeable that various needle and berry oil compositions have been observed within a really small population of J. communis L. var. communis.


2010 ◽  
Vol 5 (10) ◽  
pp. 1934578X1000501 ◽  
Author(s):  
Amel Bouzabata ◽  
Faffani Boussaha ◽  
Joseph Casanova ◽  
Félix Tomi

The chemical composition of 27 oil samples of Myrtus communis isolated from leaves collected in three locations in north–eastern Algeria was investigated by GC(RI) and 13C NMR spectroscopy. Yields ranged between 0.2-1.2% (w/w). The chemical composition of the oils was largely dominated by monoterpene hydrocarbons, with α-pinene (40.5-64.0%), 1,8-cineole (10.9-29.1%) and limonene (6.7-8.2%) being the major compounds. In all the samples, 3,3,5,5,8,8-hexamethyl-7-oxabicyclo[4.3.0]non-1(6)-ene-2,4-dione was identified (0.8-1.5%). The composition is similar to that reported for myrtle oils from Corsica, Sardinia and Tunisia, but differed from that of Moroccan and Spanish myrtle oils.


2020 ◽  
Vol 32 (7) ◽  
pp. 1630-1634
Author(s):  
Vu Thi Thu Le Vu Thi Thu Le ◽  
Lai Phuong Phuong Thao ◽  
Pham Thi Hong Minh ◽  
Hoang Thi Bich ◽  
Do Tien Lam ◽  
...  

In this study, the essential oil profile of Callicarpa candicans (Burm. f.) Hochr was presented. Samples were collected from Vietnam and the oils were extracted from fresh leaves and dry leaves by hydrodistillation method. GC-MS data and retention indices were used to identify the chemical composition. The essential oil performance achieved 0.263% for fresh leaves and 1.503% for dry leaves. A total of 47 components were identified from fresh leaves oil and 39 constituents from dry leaves oil. Chemical compositions of the two essential oils were similar, with the major components being α-gurjunene, δ-cadinene, ε-caryophyllene (β-caryophyllene) and α-selinene.


2009 ◽  
Vol 4 (8) ◽  
pp. 1934578X0900400 ◽  
Author(s):  
Asta Judzentiene ◽  
Félix Tomi ◽  
Joseph Casanova

Different techniques have been utilized to determine the composition of Artemisia absinthum (wormwood) essential oil. The oil was fractionated on a silica gel column and each fraction analyzed by GC(RI), GC-MS and 13C NMR. This allowed the identification, for the first time in A. absinthium, of two diterpenes, 9-geranyl-p-cymene and 9-geranyl-α-terpinene, and two homoditerpenes, 9-(15,16-dihydro-15-methylene)-geranyl-p-cymene and 9-(15,16-dihydro-15-methylene)-geranyl-α-terpinene. Chemical variability of A. absinthium essential oils from plants collected in the surroundings of Vilnius city over several years (1999-2007) was also shown. Chemical composition was determined by GC and GC-MS. Thujones ( cis+trans, 10.2-36.3%) and trans-sabinyl acetate (9.8-39.2%) were the two predominant constituents of almost all the investigated oils (13 out of 15 samples). The third major compound was myrcene (5.1-9.2%, in four samples), β-pinene (5.4-10.4%, in 5), linalool (4.7% in one), trans-sabinol (6.4%, in one) and 1,8-cineole (5.2-7.1%, in two). In one oil, the prevailing components were thujones ( cis+trans, 11.2%), trans-sabinene hydrate (11.0%) and trans-sabinyl acetate (8.8%), while another sample was characterized by a large quantity of trans-sabinyl acetate (55.2%) and the absence of thujones.


2016 ◽  
Vol 11 (8) ◽  
pp. 1934578X1601100 ◽  
Author(s):  
Maghnia Boussaïd ◽  
Chahrazed Bekhechi ◽  
Fewzia Atik-Bekkara ◽  
Mathieu Paoli ◽  
Joseph Casanova ◽  
...  

Very little is known about the yield and chemical composition of the essential oil isolated from cones of Tetraclinis articulata (Vahl) Masters (Cupressaceae). In continuation of our on-going work devoted to the valorisation of medicinal and aromatic plants from Tlemcen Province (North-Western Algeria), cones have been harvested in eight locations (coastal township and highlands) and 40 oil samples have been isolated by hydrodistillation. Six oil samples were analyzed by a combination of chromatographic [GC(Retention indices)] and spectroscopic techniques (GC-MS, 13C NMR). Then, the remaining 34 oil samples were analyzed by [GC(RI)] and 13C NMR and the 40 compositions were submitted to statistical analysis. Essential oil yields varied substantially from sample to sample (0.17 to 1.13%, w/w). The cone oils consisted mainly of monoterpenes, with α-pinene (47.1-73.6%) and limonene (6.5-21.9%) being the main components. (E)-β-Caryophyllene and germacrene D were the major sesquiterpenes. Diterpenes, ( Z) and ( E)-biformene were identified for the first time in T. articulata essential oil. PCA analysis of the data allowed the distinction of two groups, the second group being sub-divided into two sub-groups. Groups and sub-groups were differentiated with respect to their contents of α-pinene and limonene and, to a lesser extent, of sesquiterpenes.


2013 ◽  
Vol 8 (12) ◽  
pp. 1934578X1300801 ◽  
Author(s):  
Zana A. Ouattara ◽  
Jean Brice Boti ◽  
Coffy Antoine Ahibo ◽  
Félix Tomi ◽  
Joseph Casanova ◽  
...  

The composition of root bark oil from Cleistopholis glauca Pierre ex Engler & Diels growing wild in Ivory Coast was investigated by GC (in combination with retention indices) and 13C NMR spectroscopy after partition of hydrocarbons and oxygenated compounds on silica gel. Thirty-one compounds have been identified. C. glauca produces a sesquiterpene-rich oil, patchoulenone (33.5%), cyperene (9.5%) and germacrene D (6.6%) being the main components. Special attention was paid to the identification and quantification of germacrene C (a heat-sensitive compound) and δ-elemene, which were achieved by a combination of GC(FID) and 13C NMR spectroscopy. The composition of C. glauca root bark and leaf oils differed drastically.


2014 ◽  
Vol 9 (4) ◽  
pp. 1934578X1400900
Author(s):  
Katalin Veres ◽  
Orsolya Roza ◽  
Eszter Laczkó-Zöld ◽  
Judit Hohmann

The essential oils of Grindelia squarrosa (Pursh) Dunal and G. hirsutula Hook. & Arn. cultivated in Romania were isolated by hydrodistillation. The essential oils were analyzed by a combination of GC-FID and GC-MS. The identification of the constituents was achieved from their retention indices and comparison of their MS data with computer library database and literature data. The fifty-six identified constituents accounted for 72.1-81.3% of the oils. The oils were found to contain α-pinene, β-pinene, limonene, borneol, bornyl acetate and germacrene D as main constituents. The oils obtained from the two species showed small differences in chemical composition. However, menthol, menthone and pulegone were detected only in the essential oil of G. hirsutula.


2014 ◽  
Vol 9 (5) ◽  
pp. 1934578X1400900 ◽  
Author(s):  
Amel Bouzabata ◽  
Ange Bighelli ◽  
Lahouari Abed ◽  
Joseph Casanova ◽  
Félix Tomi

The composition of eight oil samples isolated from leaves of Eucalyptus bosistoana F. Muell., acclimatized in Tamanrasset (southern Algeria, Saharan climate), has been investigated by GC (retention indices), GC-MS and 13C NMR spectroscopy. Two groups may be distinguished. The five samples of group I have their composition dominated by p-cymene (32.0-39.5%), cryptone (11.5-15.6%), 1,8-cineole (7.8-10.5%) and spathulenol (6.8-16.5%). The three oil samples of group II contained mainly 1,8-cineole (55.3-63.9%) and α-pinene (11.6-12.1%).


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