Chemical composition and cytotoxic activity of the leaf essential oil of Eugenia zuchowskiae from Monteverde, Costa Rica

2007 ◽  
Vol 61 (4) ◽  
pp. 414-417 ◽  
Author(s):  
Ramona A. Cole ◽  
Anita Bansal ◽  
Debra M. Moriarity ◽  
William A. Haber ◽  
William N. Setzer
Keyword(s):  
Costa Rica ◽  
Chemical Composition ◽  
Essential Oil ◽  
Cytotoxic Activity ◽  
Leaf Essential Oil

scholarly journals Leaf Essential Oil of Manekia naranjoana (Piperaceae) from Costa Rica and its Cytotoxic Activity

2011 ◽  
Vol 6 (1) ◽  
pp. 1934578X1100600 ◽  
Author(s):  
Carlos Chaverri ◽  
Cecilia Díaz ◽  
José F. Cicció
Keyword(s):  
Costa Rica ◽  
Chemical Composition ◽  
Essential Oil ◽  
Tumor Cell ◽  
Cytotoxic Activity ◽  
Tumor Cell Lines ◽  
Capillary Gc ◽  
Leaf Oil ◽  
Leaf Essential Oil ◽  
Low Toxicity

The chemical composition of the leaf oil of Manekia naranjoana (C. DC.) Callejas (Piperaceae) from Costa Rica was analyzed by capillary GC/FID and GC/MS. Fifty-five compounds were identified. Major compounds from the leaf oil were β-pinene (30.6%), α-pinene (18.8%), limonene (13.7%), and β-caryophyllene (6.1%). The oil presented very low toxicity to tumor and non-tumor cell lines, even though it contains components, such as α- and β-pinene, limonene and others, which have been shown to be cytotoxic. This is the first report of the chemical composition of the essential oil obtained from this species.

scholarly journals Composition and in-vitro CytotoxicActivities of the Leaf Essential Oil of Beilschmiedia erythrophloia from Taiwan

2013 ◽  
Vol 8 (1) ◽  
pp. 1934578X1300800
Author(s):  
Yu-Chang Su ◽  
Chen-Lung Ho
Keyword(s):  
Chemical Composition ◽  
Essential Oil ◽  
Cytotoxic Activity ◽  
Cancer Cells ◽  
Cytotoxic Activities ◽  
Anticancer Activities ◽  
Leaf Essential Oil ◽  
Main Components ◽  
Type Apparatus

This study investigated the chemical composition and in-vitro cytotoxic activities of the essential oil isolated from the leaf of Beilschmiedia erythrophloia. The essential oil was isolated using hydrodistillation in a Clevenger-type apparatus, and characterized by GC-FID and GC-MS. Fifty-five compounds were identified, representing 100% of the oil. The main components identified were β-caryophyllene (22.6%), α-humulene (21.9%), terpinen-4-ol (5.3%), cis-β-ocimene (5.1%), sabinene (5.0%) and limonene (4.5%). The anticancer activities of oil were evaluated. The results showed that the oil exhibited cytotoxic activity against human oral, liver, lung, colon, melanoma, and leukemic cancer cells.

scholarly journals Analysis of the Leaf Essential Oil of Stauranthus perforatus from Monteverde, Costa Rica

2006 ◽  
Vol 1 (3) ◽  
pp. 1934578X0600100 ◽  
Author(s):  
Jennifer M. Schmidt ◽  
William N. Setzer
Keyword(s):  
Costa Rica ◽  
Chemical Composition ◽  
Essential Oil ◽  
Germacrene D ◽  
Leaf Essential Oil ◽  
Oil Components

The leaf essential oil of Stauranthus perforatus Leibm. (Rutaceae) from Monteverde, Costa Rica, was isolated by hydrodistillation and the chemical composition determined by GC–MS. The most abundant essential oil components were α-pinene, germacrene D, and α-cadinol.

scholarly journals Composition and in vitro Anticancer Activities of the Leaf Essential Oil of Neolitsea variabillima from Taiwan

2013 ◽  
Vol 8 (4) ◽  
pp. 1934578X1300800 ◽  
Author(s):  
Yu-Chang Su ◽  
Kuan-Ping Hsu ◽  
Eugene I-Chen Wang ◽  
Chen-Lung Ho
Keyword(s):  
Chemical Composition ◽  
Essential Oil ◽  
Cytotoxic Activity ◽  
Cancer Cells ◽  
Anticancer Activities ◽  
Leaf Oil ◽  
Leaf Essential Oil ◽  
Main Components ◽  
Type Apparatus

This study investigated the chemical composition and in vitro anticancer activities of the essential oil isolated from the leaf of Neolitsea variabillima. The essential oil was isolated using hydrodistillation in a Clevenger-type apparatus, and characterized by GC-FID and GC-MS. Sixty-seven compounds were identified, representing 100% of the oil. The main components identified were trans-β-ocimene (13.4%), α-cadinol (10.5%), terpinen-4-ol (9.3%), τ-cadinol (9.2%), β-caryophyllene (8.8%), and sabinene (6.7%). The anticancer activities of oil were evaluated. The results showed that the oil exhibited cytotoxic activity against human oral, liver, lung, colon, melanoma, and leukemic cancer cells. The presence of β-caryophyllene, τ-cadinol, and α-cadinol significantly contributed to the anticancer activities of N. variabillima leaf oil.

scholarly journals Caryophyllene-Rich Essential Oil of Didymocarpus Tomentosa: Chemical Composition and Cytotoxic Activity

2012 ◽  
Vol 7 (11) ◽  
pp. 1934578X1200701 ◽  
Author(s):  
Prameela Javarayi Gowda ◽  
Hanumanthaiah Ramakrishnaiah ◽  
Venkatarangaiah Krishna ◽  
Sivakrishna Narra ◽  
Nataraj Jagannath
Keyword(s):  
Chemical Composition ◽  
Essential Oil ◽  
Tumor Cell ◽  
Cytotoxic Activity ◽  
Cell Line ◽  
Mtt Assay ◽  
Tumor Cell Line ◽  
Caryophyllene Oxide ◽  
Leaf Oil ◽  
Leaf Essential Oil

The essential oil from the leaves of Didymocarpus tomentosa was extracted by hydrodistillation and analyzed by GC/FID and GC/MS. Twenty five constituents amounting to 81.6% of the oil were identified. The leaf oil contained 78.7% sesquiterpenes and 2.9% monoterpenes. The leaf essential oil of D. tomentosa is a unique caryophyllene-rich natural source containing β-caryophyllene, caryophyllene oxide, α-humulene and humulene oxide. The cytotoxic activity of the oil was determined by the BSLT using shrimp larva and the MTT assay using HeLa tumor cell line. The oil showed significant cytotoxic activity with LC50 and IC50 values of 12.26 and 11.4 μg/mL, respectively. This is the first report on the chemical composition and cytotoxic activity of the essential oil of D. tomentosa.

scholarly journals Chemical Composition and Cytotoxic Activity of Chenopodium ambrosioides L. Essential Oil from Togo

1970 ◽  
Vol 44 (4) ◽  
pp. 435-440 ◽  
Author(s):  
Koffi Koba ◽  
Guyon Catherine ◽  
Christine Raynaud ◽  
Jean-Pierre Chaumont ◽  
Komla Sanda ◽  
...  
Keyword(s):  
Chemical Composition ◽  
Essential Oil ◽  
Cytotoxic Activity ◽  
Cell Line ◽  
Human Cell Line ◽  
In Vitro Cytotoxicity ◽  
Chenopodium Ambrosioides ◽  
Ic50 Value ◽  
Leaf Essential Oil

The leaf essential oil of Chromolaena odorata L. (Chenopodiaceae) from Togo were steam-distilled, analyzed by GC and GC-MS for chemical composition and investigated in vitro for its potential cytotoxic activity on human epidermic cell line HaCat. The chemical composition showed that the main constituents of essential oil sample were respectively ascaridole (51.12 %), p-cymene (19.88 %), neral (8.70%) and geraniol (7.55%). The in vitro cytotoxicity bioassays on human cell line HaCaT revealed moderate toxicity level of C. ambrosioides essential oil IC50 with 700 μL.mL-1. Pure commercial neral standard showed high toxicity with IC50 value of 100 μL.mL-1). Conversely, pure ascaridole p-cymene and geraniol standards appeared almost non-toxic (IC50 >1000 μL.mL-1), proving the major role played by neral in the overall toxicity showed by the C. ambrosiodes oil sample tested in this work. Keywords: Chenopodium ambrosioides; Essential oil; Ascaridole; p-cymene; HaCaT cell line; Cytotoxicity. DOI: 10.3329/bjsir.v44i4.4594 Bangladesh J. Sci. Ind. Res. 44(4), 435-440, 2009

scholarly journals Chemical Composition and Cytotoxic Activity of the Leaf Essential Oil of Ocotea tonduzii from Monteverde, Costa Rica

2007 ◽  
Vol 2 (7) ◽  
pp. 1934578X0700200 ◽  
Author(s):  
Anita Bansal ◽  
Debra M. Moriarity ◽  
Sayaka Takaku ◽  
William N. Setzer
Keyword(s):  
Costa Rica ◽  
Chemical Composition ◽  
Essential Oil ◽  
Cytotoxic Activities ◽  
Germacrene D ◽  
Leaf Oil ◽  
Leaf Essential Oil ◽  
Oil Components ◽  
Mcf 7

The leaf essential oil of Ocotea tonduzii from Monteverde, Costa Rica has been obtained by hydrodistillation and analyzed by GC-MS. The principal constituents of O. tonduzii leaf oil were the monoterpenes α-pinene (41.4%) and pinene (25.1%) and the sesquiterpenes α-humulene (6.9%), β-caryophyllene (5.8%), and germacrene D (3.8%). O. tonduzii leaf oil was notably cytotoxic on MCF-7, MDA-MB-231, MDA-MB-468, and UACC-257 cells in vitro. The major essential oil components showed cytotoxic activities comparable to doxorubicin ( LC50, 20–70 μg/mL).

scholarly journals Chemical Composition of the Leaf Essential Oil of Casimiroa Edulis La Llave & Lex. (Rutaceae) from Monteverde, Costa Rica

2009 ◽  
Vol 4 (3) ◽  
pp. 1934578X0900400 ◽  
Author(s):  
Sarah L. Miller ◽  
William A. Haber ◽  
William N. Setzer
Keyword(s):  
Costa Rica ◽  
Chemical Composition ◽  
Essential Oil ◽  
Traditional Use ◽  
Sesquiterpene Hydrocarbons ◽  
Germacrene D ◽  
Casimiroa Edulis ◽  
Leaf Oil ◽  
Leaf Essential Oil

The leaf essential oil of Casimiroa edulis (Rutaceae), collected from Monteverde, Costa Rica, has been obtained by hydrodistillation and analyzed by GC-MS. The leaf oil was dominated by sesquiterpene hydrocarbons, predominately germacrene D (16-22%) and ( E)-caryophyllene (16-17%), consistent with the traditional use of this plant as a sedative, sleep inducer and hypotensive.

scholarly journals Essential oil Composition of Dendropanax Gonatopodus from Monteverde, Costa Rica. An ab Initio Examination of Aromadendrane Sesquiterpenoids

2008 ◽  
Vol 3 (9) ◽  
pp. 1934578X0800300 ◽  
Author(s):  
William N. Setzer
Keyword(s):  
Costa Rica ◽  
Chemical Composition ◽  
Essential Oil ◽  
Ab Initio ◽  
Density Functional ◽  
Essential Oil Composition ◽  
Oil Composition ◽  
Hartree Fock ◽  
Leaf Oil ◽  
Leaf Essential Oil

The leaf essential oil of Dendropanax gonatopodus from Monteverde, Costa Rica, has been obtained by hydrodistillation and the chemical composition determined by GC-MS. The major components in the leaf oil were ( E)-2-hexenal (16.9%), terpinolene (14.8%), δ-cadinene (13.5%), ( E)-caryophyllene (9.9%), and α-copaene (7.3%). Minor amounts of the aromadendrane sesquiterpenoids aromadendrene (0.3%), alloaromadendrene (0.3%), spathulenol (0.6%) and globulol (0.6%) were also detected. An ab initio investigation of the aromadendrane sesquiterpenoids has been carried out using both density functional (B3LYP/6-31G*) and post Hartree-Fock (MP2/6-31G**) methods. The calculated relative energies of the aromadendranes belie their relative concentrations generally observed in essential oil compositions.

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