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1.
Chem Biodivers ; 13(1): 66-76, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26765353

ABSTRACT

The hydrodistilled oil of Cryptocarya massoy bark was characterized by GC-FID and GC/MS analyses, allowing the identification of unusual C10 massoia lactone (3, 56.2%), C12 massoia lactone (4, 16.5%), benzyl benzoate (1, 12.7%), C8 massoia lactone (3.4%), δ-decalactone (5, 1.5%), and benzyl salicylate (2, 1.8%) as main constituents. The phytotoxic activities of the oil, three enriched fractions (lactone-rich, ester-rich, and sesquiterpene-rich), and four constituents (compounds 1, 2, 5, and δ-dodecalactone (6)) against Lycopersicon esculentum and Cucumis sativus seeds and seedlings were screened. At a concentration of 1000 µl/l, the essential oil and the massoia lactone-rich fraction caused a complete inhibition of the germination of both seeds, and, when applied on tomato plantlets, they induced an 85 and 100% dieback, respectively. These performances exceeded those of the well-known phytotoxic essential oils of Syzygium aromaticum and Cymbopogon citratus, already used in commercial products for the weed and pest management. The same substances were also evaluated against four phytopathogenic bacteria and ten phytopathogenic fungi, providing EC50 values against the most susceptible strains in the 100-500 µl/l range for the essential oil and in the 10-50 µl/l range for compound 6 and the lactone-rich fraction. The phytotoxic behavior was related mainly to massoia lactones and benzyl esters, while a greater amount of 6 may infer a good activity against some phytopathogenic fungi. Further investigations of these secondary metabolites are warranted, to evaluate their use as natural herbicides.


Subject(s)
Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/pharmacology , Antifungal Agents/chemistry , Antifungal Agents/pharmacology , Bacteria/drug effects , Cryptocarya/chemistry , Fungi/drug effects , Plant Oils/pharmacology , Seeds/drug effects , Anti-Bacterial Agents/isolation & purification , Anti-Bacterial Agents/toxicity , Antifungal Agents/isolation & purification , Antifungal Agents/toxicity , Cucumis sativus/drug effects , Cucumis sativus/growth & development , Dose-Response Relationship, Drug , Solanum lycopersicum/drug effects , Solanum lycopersicum/growth & development , Microbial Sensitivity Tests , Molecular Structure , Plant Bark/chemistry , Plant Oils/chemistry , Plant Oils/isolation & purification , Seeds/growth & development , Structure-Activity Relationship
2.
J Oleo Sci ; 63(12): 1243-50, 2014.
Article in English | MEDLINE | ID: mdl-25391685

ABSTRACT

Nowadays, data concerning the composition of Caryodendron orinocense Karst. (Euphorbiaceae) and Bactris gasipaes Kunth (Arecaceae) seed oils are lacking. In light of this fact, in this paper fatty acids and unsaponifiable fraction composition have been determined using GC-MS, HPLC-DAD (Diode Array Detector), NMR approaches and possible future applications have been preliminary investigated through estimation of antioxidant activity, performed with DPPH test. For C. orinocense linoleic acid (85.59%) was the main component, lauric (33.29%) and myristic (27.76%) acids were instead the most abundant in B. gasipaes. C. orinocense unsaponifiable fraction (8.06%) evidenced a remarkable content of ß-sitosterol, campesterol, stigmasterol, squalene and vitamin E (816 ppm). B. gasipaes revealed instead ß-sitosterol and squalene as main constituents of unsaponifiable matter (3.01%). Antioxidant capacity evidenced the best performance of C. orinocense seed oil. These preliminary results could be interesting to suggest the improvement of the population's incomes from Amazonian basin. In particular the knowledge of chemical composition of C. orinocense and B. gasipaes oils could be helpful to divulge and valorize these autochthones plants.


Subject(s)
Antioxidants , Arecaceae/chemistry , Euphorbiaceae/chemistry , Fatty Acids/isolation & purification , Fatty Acids/pharmacology , Nuts/chemistry , Plant Oils/chemistry , Seeds/chemistry , Cholesterol/analogs & derivatives , Cholesterol/analysis , Cholesterol/isolation & purification , Cholesterol/pharmacology , Chromatography, High Pressure Liquid , Fatty Acids/analysis , Free Radical Scavengers , Gas Chromatography-Mass Spectrometry , Lauric Acids/analysis , Lauric Acids/isolation & purification , Lauric Acids/pharmacology , Linoleic Acid/analysis , Linoleic Acid/isolation & purification , Linoleic Acid/pharmacology , Magnetic Resonance Spectroscopy , Myristic Acid/analysis , Myristic Acid/isolation & purification , Myristic Acid/pharmacology , Phytosterols/analysis , Phytosterols/isolation & purification , Phytosterols/pharmacology , Plant Oils/isolation & purification , Sitosterols/analysis , Sitosterols/isolation & purification , Sitosterols/pharmacology , Squalene/analysis , Squalene/isolation & purification , Squalene/pharmacology , Stigmasterol/analysis , Stigmasterol/isolation & purification , Stigmasterol/pharmacology , Vitamin E/analysis , Vitamin E/isolation & purification , Vitamin E/pharmacology
3.
Phytother Res ; 28(8): 1173-81, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24395450

ABSTRACT

Eleven decoctions, obtained from indian plants widely used in ayurvedic medicine, have been investigated as a possible source of molecules exhibiting biological activity on the interaction between DNA and NF-kB, a transcription factor involved in the expression of proinflammatory genes. Cystic fibrosis (CF) cell line stimulated by TNF-α has been used as inflammatory cellular model to determinate interleukin-8 (IL-8), one of the most relevant pro-inflammatory mediator in CF regulated by the NF-kB. The chemical characterization of these 11 decoctions by spectrophotometric analysis and NMR fingerprinting highlighted that sugars and polyphenols seemed to be the main compounds. Our results demonstrated that Azadirachta indica, Terminalia bellerica, Terminalia chebula, Hemidesmus indicus, Emblica officinalis and Swertia chirata are the most active decoctions in inhibiting NF-kB/DNA interactions by EMSA assay and in reducing pro-inflammatory IL- 8 expression in CF cells at IC50 concentrations by Real-Time and Bio-plex analyses. Finally, we observed the increase of all inhibitory activities with the rise of total polyphenols, procyanidins and flavonoids, except for the levels of IL-8 mRNA accumulation, that were as high as flavonoid content grown up by the statistical multivariate analyses. In conclusion, these six decoctions might be interesting to explore new anti-inflammatory treatments for diseases, such as CF.


Subject(s)
Interleukin-8/metabolism , Medicine, Ayurvedic , Plant Extracts/pharmacology , Azadirachta/chemistry , Cell Line , Cystic Fibrosis , Hemidesmus/chemistry , Humans , NF-kappa B/metabolism , Phyllanthus emblica/chemistry , Plant Extracts/chemistry , Polyphenols/chemistry , Swertia/chemistry , Terminalia/chemistry , Tumor Necrosis Factor-alpha/pharmacology
4.
Food Chem ; 139(1-4): 439-47, 2013 Aug 15.
Article in English | MEDLINE | ID: mdl-23561129

ABSTRACT

The Amazonian Croton lechleri stem bark essential oil was tested for its anti-mutagenic potential by performing the Ames test against heterocyclic amines (HCAs), in continuing research on applicative functional profile of this phytocomplex as food ingredient (Rossi et al., 2011). Salmonella typhimurium strain TA98 was used with and without metabolic activation (S9 mix). The anti-mutagenic properties was assayed with the following HCAs: 2-amino-3-methylimidazo-[4,5-f]quinoline (IQ), 2-amino-3,4-dimethylimidazo-[4,5-f]quinoline (MeIQ), 2-amino-3,8-dimethylimidazo-[4,5-f]quinoxaline (MeIQx), the imidazoles 2-amino-6-methyldipyrido-[1,2-a:3',2'-d]imidazole (Glu-P-1) and 2-aminodipirydo-[1,2-a:3',2'-d]imidazole (Glu-P-2). All HCAs with S9 induced mutagenicity at 10(-10) mol/plate. Without S9, IQ and MeIQ showed mutagenicity at 10(-8) mol/plate, MeIQx and Glu-P-1 at 10(-5) mol/plate, while Glu-P-2 was inactive. In presence of HACs (10(-9) mol/plate), C. lechleri essential oil was tested for mutagen-protective properties (concentration range: 0.01-0.10 mg/plate) taking the Highest Uneffective Dose (HUD) as threshold reference. With S9 mix, C. lechleri essential oil displayed a significant reduction of revertants at 0.05 mg/plate, from 21% to 34%. The essential oil showed mutagen-protective efficacy against IQ and MeIQ tested as direct mutagens (10(-7) mol/plate), with a revertants percentage reduction of 39% and 40%, respectively. No anti-mutagen capacity was noted for MeIQx and Glu-P-1 (10(-5) mol/plate). Since HACs are known as possible colon and liver cancer inducers, C. lechleri essential oil was tested for its cytotoxicity and anti-proliferative capacity against LoVo and HepG2 cancer cell lines showing IC50 of 74.95±0.05 µg/ml (LoVo) and 82.28±0.03 µg/ml (HepG2), displaying a promising role of this essential oil as a functional food ingredient with interesting mutagen preventing properties.


Subject(s)
Amines/toxicity , Antimutagenic Agents/pharmacology , Euphorbiaceae/chemistry , Food Additives/pharmacology , Oils, Volatile/pharmacology , Plant Bark/chemistry , Plant Oils/pharmacology , Amines/chemistry , Antimutagenic Agents/analysis , Cell Line , Cell Proliferation/drug effects , Cooking , Food Additives/analysis , Food Analysis , Humans , Molecular Structure , Mutagens/chemistry , Mutagens/toxicity , Oils, Volatile/analysis , Plant Oils/analysis , Salmonella typhimurium/drug effects , Salmonella typhimurium/genetics
5.
Planta Med ; 78(18): 1927-31, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23154840

ABSTRACT

Juniperus excelsa fruit essential oil as well as J. oxycedrus, Cedrus libani, and Pinus pinea wood essential oils have been obtained with yields between 2.2 ± 0.3 % to 3.4 ± 0.5 % and analyzed by gas chromatography. Sesquiterpenes mainly characterized C. libani and J. oxycedrus essential oils, while in P. pinea and J. excelsa, monoterpenes were the most abundant compounds. In J. oxycedrus, cis-calamenene (7.8 %), cuparene (3.8 %), and cis-thujopsenal (2.0 %) have been detected for the first time. The cytotoxic activity of these essential oils against drug-sensitive CCRF-CEM and multidrug-resistant P-glycoprotein-expressing CEM/ADR5000 leukemia cells has been investigated (IC50 values: 29.46 to 61.54 µg/mL). Remarkably, multidrug-resistant CEM/ADR5000 cells did not reveal cross-resistance, indicating that these essential oils might be useful to treat otherwise drug-resistant and refractory tumors.


Subject(s)
Antineoplastic Agents, Phytogenic/pharmacology , Drug Resistance, Neoplasm/drug effects , Leukemia/drug therapy , Oils, Volatile/chemistry , Phytotherapy , Plants, Medicinal/chemistry , Tumor Cells, Cultured/drug effects , Antineoplastic Agents, Phytogenic/chemistry , Antineoplastic Agents, Phytogenic/isolation & purification , Cedrus/chemistry , Drug Resistance, Multiple/drug effects , Fruit/chemistry , Humans , Juniperus/chemistry , Lebanon , Monoterpenes/isolation & purification , Oils, Volatile/pharmacology , Pinus/chemistry , Sesquiterpenes/isolation & purification , Wood/chemistry
6.
Molecules ; 17(10): 12393-405, 2012 Oct 22.
Article in English | MEDLINE | ID: mdl-23090020

ABSTRACT

Fourteen brands of resveratrol-containing nutraceuticals were evaluated in order to verify their actual resveratrol content and to control if their health-promoting properties are related to manufacturing quality. Products included pure resveratrol capsules or multi-ingredient formulations with standardized amounts of resveratrol and other phytochemicals. Samples were analyzed for total trans-resveratrol, flavonoids, procyanidin, polyphenol content and the results were compared with the content declared on-label. Only five out of 14 brands had near label values, compliant with Good Manufacturing Practices (GMP) requirements (95-105% content of active constituent), four products were slightly out of this range (83-111%) and three were in the 8-64% range. Two samples were below the limit of detection. The greater the difference between actual and labeled resveratrol content, the lower was the antioxidant and antiproliferative activity strength. Dietary supplements containing pure trans-resveratrol exhibited a greater induction of differentiation towards human leukemic K562 cells when compared to multicomponent products. Great differences currently exist among resveratrol food supplements commercially available and GMP-grade quality should not be taken for granted. On the other side, dosages suggested by most "pure", "high-dosage" supplements may allow a supplementation level adequate to obtain some of the purported health benefits.


Subject(s)
Commerce/standards , Dietary Supplements/standards , Stilbenes/standards , Antioxidants/analysis , Biflavonoids/analysis , Catechin/analysis , Cell Differentiation/drug effects , Cell Proliferation/drug effects , Chromatography, High Pressure Liquid , Discriminant Analysis , Erythroid Cells/cytology , Erythroid Cells/drug effects , Erythroid Cells/metabolism , Flavonoids/analysis , Food Labeling , Humans , K562 Cells , Least-Squares Analysis , Polyphenols/analysis , Proanthocyanidins/analysis , Resveratrol , Stilbenes/pharmacology
7.
Pharm Biol ; 48(7): 834-8, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20645785

ABSTRACT

The essential oil of fruits of Cuminum cyminum L. (Apiaceae), from India, was analyzed by GC and GC-MS, and its antifungal activity was tested on dermatophytes and phytopathogens, fungi, yeasts and some new Aspergilli. The most abundant components were cumin aldehyde, pinenes, and p-cymene, and a fraction of oxygenate compounds such as alcohol and epoxides. Because of the large amount of the highly volatile components in the cumin extract, we used a modified recent technique to evaluate the antifungal activity only of the volatile parts at doses from 5 to 20 microL of pure essential oil. Antifungal testing showed that Cuminum cyminum is active in general on all fungi but in particular on the dermatophytes, where Trichophyton rubrum was the most inhibited fungus also at the lowest dose of 5 microL. Less sensitive to treatment were the phytopathogens.


Subject(s)
Antifungal Agents/pharmacology , Arthrodermataceae/drug effects , Cuminum/chemistry , Fungi/drug effects , Oils, Volatile/pharmacology , Yeasts/drug effects , Antifungal Agents/isolation & purification , Arthrodermataceae/growth & development , Arthrodermataceae/metabolism , Fungi/growth & development , Fungi/metabolism , Medicine, Ayurvedic , Microbial Sensitivity Tests , Oils, Volatile/isolation & purification , Trichophyton/drug effects , Trichophyton/growth & development , Trichophyton/metabolism , Yeasts/growth & development , Yeasts/metabolism
8.
J Agric Food Chem ; 58(9): 5438-43, 2010 May 12.
Article in English | MEDLINE | ID: mdl-20392042

ABSTRACT

A new approach for removing monoterpenes (MTs) from bergamot oil by selective inclusion in deoxycholic acid (DCA) is proposed. The inclusion process is very efficient, the included fraction being composed mainly of limonene (71.7%) and gamma-terpinene (19.8%). On the other hand, the deterpenated bergamot oil fraction showed for the linalool and linalyl acetate derivatives significant increases from 16.6 and 21.4% to 18.3 and 42.2%, respectively. The major advantages of this methodology are its simplicity, the mild conditions employed, and the quantitative recovery of both host (DCA) and guest (monoterpenes) compounds. Differential scanning calorimetry (DSC), thermal gravimetry (TG), powder X-ray diffractometry (XRPD), infrared spectroscopy (IR), and proton magnetic resonance ((1)H NMR) analysis were used to investigate and characterize the inclusion compounds.


Subject(s)
Deoxycholic Acid/chemistry , Monoterpenes/isolation & purification , Plant Oils/chemistry , Calorimetry, Differential Scanning , Magnetic Resonance Spectroscopy , Spectrophotometry, Infrared , X-Ray Diffraction
9.
Biotechnol Lett ; 28(11): 805-10, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16786245

ABSTRACT

Fungi from Amazonian forest soil (Ecuador) and an Italian factory were screened for Baeyer-Villiger (BV) oxidation of bicyclo [3.2.0]hept-2-en-6-one to 2-oxabicyclo[3.3.0]oct-6-en-3-one (Corey's lactone). Isolates of Fusarium sp. and F. solani produced the (+)-(1R,5S)-lactone while isolates of Aspergillus terricola and A. amazonicus afforded the (-)-(1S,5R)-lactone. Highest conversions (85% yield and 70% enantiomeric excess) were obtained with A. amazonicus grown in presence of 2.7 mM titanium dioxide.


Subject(s)
Aspergillus/metabolism , Bridged Bicyclo Compounds/metabolism , Fusarium/metabolism , Aspergillus/growth & development , Biotransformation/physiology , Fusarium/growth & development , Oxidation-Reduction , Stereoisomerism , Titanium
10.
J Agric Food Chem ; 52(11): 3486-91, 2004 Jun 02.
Article in English | MEDLINE | ID: mdl-15161220

ABSTRACT

Wild Amazonian basil Ocimum micranthum Willd. (O. campechianum Mill.) Labiatae essential oil was analyzed by GC and GC-MS: 31 compounds were identified. The main components were eugenol (46.55 +/- 5.11%), beta-caryophyllene (11.94 +/- 1.31%), and beta-elemene (9.06 +/- 0.99%), while a small amount of linalool (1.49 +/- 0.16%) was detected. The oil was tested for its in vitro food-related biological activities and compared with common basil Ocimum basilicum and Thymus vulgaris commercial essential oils. Radical scavenging activity was evaluated employing 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay. The oil exerted a good capacity to act as a nonspecific donor of hydrogen atoms or electrons when checked in the diphenylpicrylhydrazyl assay, quenching 76,61 +/- 0.33% of the radical, with values higher than those reported by reference oils. In the beta-carotene bleaching test, the oil provided an antioxidant efficacy comparable with that of O. basilicum and T. vulgaris essential oils. These data were confirmed by photochemiluminescence, where the oil showed a remarkable antioxidant capacity (2.39 +/- 0.1), comparable to that of Trolox and vitamin E, and higher than the other essential oils. Antibacterial activity of O. micranthum essential oil was evaluated against Gram positive and Gram negative bacterial strains. The oil showed a dose-dependent antifungal activity against pathogenic and food spoiling yeasts.


Subject(s)
Ocimum/chemistry , Oils, Volatile/chemistry , Anti-Bacterial Agents/analysis , Anti-Bacterial Agents/pharmacology , Antioxidants/analysis , Antioxidants/pharmacology , Bacteria/drug effects , Chromatography, Gas , Gas Chromatography-Mass Spectrometry
11.
J Org Chem ; 67(16): 5802-6, 2002 Aug 09.
Article in English | MEDLINE | ID: mdl-12153284

ABSTRACT

The asymmetric epoxidation of substituted cinnamic acids has been obtained in the presence of different keto bile acid derivatives as optically active carbonyl inducers and Oxone as oxygen source. Predominant or almost exclusive formation of both enantiomeric epoxides is obtained (ee up to 95%) depending on the specific substitution at carbons C(7) and C(12) of the bile acid.


Subject(s)
Bile Acids and Salts , Cinnamates/chemical synthesis , Epoxy Compounds , Cinnamates/chemistry , Indicators and Reagents , Ketones , Magnetic Resonance Spectroscopy , Molecular Conformation , Stereoisomerism , Structure-Activity Relationship
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