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1.
Bioorg Chem ; 116: 105333, 2021 11.
Article in English | MEDLINE | ID: mdl-34537516

ABSTRACT

Natural products--polyoxygenated cyclohexenes exhibited potent anti-tumor activity, such as zeylenone, which is a natural product isolated from Uvaria grandiflora Roxb. This article will attempt to establish a gram-scale synthesis method of (+)-zeylenone and explain the structure-activity relationship of this kind of compound. Total synthesis of (+)-zeylenone was completed in 13 steps with quinic acid as the starting material in 9.8% overall yield. The highlight of the route was the control of the three carbon's chirality by single step dihydroxylation. In addition, different kinds of derivatives were designed and synthesized. Cell Counting Kit-8 (CCK8) assay was used for evaluating antitumor activity against three human cancer cell lines. The structure--activity relationship suggested that compounds with both absolute configurations exhibited tumor-suppressive effects. Moreover, hydroxyls at the C-1/C-2 position were crucial to the activity, and the esterification of large groups at C-1 hydroxyl eliminated the activity. Hydroxyl at the C-3 position was also important as proper ester substituent could increase the potency.


Subject(s)
Antineoplastic Agents, Phytogenic/pharmacology , Cyclohexanes/pharmacology , Dioxanes/pharmacology , Uvaria/chemistry , Animals , Antineoplastic Agents, Phytogenic/chemistry , Antineoplastic Agents, Phytogenic/isolation & purification , Cell Proliferation/drug effects , Cell Survival/drug effects , Cyclohexanes/chemistry , Cyclohexanes/isolation & purification , Dioxanes/chemistry , Dioxanes/isolation & purification , Dose-Response Relationship, Drug , Drug Screening Assays, Antitumor , Humans , Mice , Molecular Structure , Stereoisomerism , Structure-Activity Relationship , Tumor Cells, Cultured
2.
Angew Chem Int Ed Engl ; 60(44): 23590-23595, 2021 10 25.
Article in English | MEDLINE | ID: mdl-34463419

ABSTRACT

Shape complementarity is a biological craft for precisely binding substrates at protein-protein interfaces. An analogy to such a function can be drawn conceptually for crystalline porous solids; yet the manifested entities are rare in reticular chemistry. The bottleneck-shaped pores carved out of a metal-organic framework, Zn(MIBA)2 (aka. MAF-stu-13), can perfectly accommodate benzene molecules. Remarkably, its framework adapts to the optimal guest binding-the enhanced host-guest interactions in the neck in turn minimize the guest-guest repulsion in the pore to the extent it turns into attraction-as demonstrated by the combined X-ray structural and DFT computational studies. This adaptive material can be used for liquid-phase production of ultrahigh-purity (≥99 %) cyclohexane, achieving a balance between uptake capacity and separation selectivity and surpassing the performances of other porous and nonporous crystals reported recently (e.g. product purity 99.4 % vs. 97.5 % to date).


Subject(s)
Cyclohexanes/isolation & purification , Imidazoles/chemistry , Metal-Organic Frameworks/chemistry , Cyclohexanes/chemistry , Models, Molecular , Particle Size
3.
J Nat Prod ; 83(3): 730-737, 2020 03 27.
Article in English | MEDLINE | ID: mdl-32163285

ABSTRACT

Two new helvolic acid analogues (1 and 2) and one new fumagillin derivative containing an octahydroisobenzofuran moiety (3), together with four known compounds (4-7), were isolated from an Aspergillus terreus, isolated from soil collected from Mauna Kea, the highest mountain in Hawaii. Compound 4 was recorded in SciFinder with a CAS Registry Number of 1379525-35-5, but it was not documented in the cited reference (ACS Chem. Biol. 2012, 7, 137). The structures of compounds 1-4 were elucidated by NMR spectroscopy and HRMS and ECD analysis. Compounds 5 and 6 showed significant inhibitory activity against NF-κB with IC50 values of 2.7 ± 2.6 and 6.5 ± 0.8 µM, respectively. Compounds 1 and 2 were active against S. aureus with MICs of 6.25 and 6.25 µg/mL, respectively, while compound 5 inhibited E. coli with an MIC of 3.12 µg/mL.


Subject(s)
Anti-Bacterial Agents/pharmacology , Aspergillus/chemistry , Cyclohexanes/pharmacology , Fatty Acids, Unsaturated/pharmacology , Fusidic Acid/analogs & derivatives , NF-kappa B/antagonists & inhibitors , Anti-Bacterial Agents/isolation & purification , Biological Products/isolation & purification , Biological Products/pharmacology , Cyclohexanes/isolation & purification , Escherichia coli/drug effects , Fatty Acids, Unsaturated/isolation & purification , Fusidic Acid/isolation & purification , Fusidic Acid/pharmacology , HEK293 Cells , Hawaii , Humans , Microbial Sensitivity Tests , Molecular Structure , Sesquiterpenes/isolation & purification , Sesquiterpenes/pharmacology , Staphylococcus aureus/drug effects
4.
Molecules ; 24(19)2019 Oct 01.
Article in English | MEDLINE | ID: mdl-31581527

ABSTRACT

The band shapes and band positions of near-infrared (NIR) and Raman spectra change depending on the concentrations of specific chemical functionalities in a multicomponent system. To elucidate these effects in more detail and clarify their impact on the analytical measurement techniques and evaluation procedures, NIR transmission spectra and Raman spectra of two organic liquid three-component systems with variable compositions were analyzed by two different multivariate calibration procedures, partial least squares (PLS) and classical least-squares (CLS) regression. Furthermore, the effect of applying different concentration units (volume percent (%V) and weight percent (%W) on the performance of the two calibration procedures have been tested. While the mixtures of benzene/cyclohexane/ethylbenzene (system 1) can be regarded as a blended system with comparatively low molecular interactions, hydrogen bonding plays a dominant role in the blends of ethyl acetate/1-heptanol/1,4-dioxane (system 2). Whereas system 1 yielded equally good calibrations by PLS and CLS regression, for system 2 acceptable results were only obtained by PLS regression. Additionally, for both sample systems, Raman spectra generally led to lower calibration performance than NIR spectra. Finally, volume and weight percent concentration units yielded comparable results for both chemometric evaluation procedures.


Subject(s)
Hydrocarbons, Cyclic/isolation & purification , Benzene Derivatives/isolation & purification , Calibration , Cyclohexanes/isolation & purification , Hydrogen Bonding , Least-Squares Analysis , Molecular Weight , Spectroscopy, Near-Infrared , Spectrum Analysis, Raman
5.
J Nat Prod ; 80(1): 141-148, 2017 01 27.
Article in English | MEDLINE | ID: mdl-28099006

ABSTRACT

Human pancreatic cancer cell lines have a remarkable tolerance to nutrition starvation, which enables them to survive under a tumor microenvironment. The search for agents that preferentially inhibit the survival of cancer cells under low nutrient conditions represents a novel antiausterity strategy in anticancer drug discovery. In this investigation, a methanol extract of the rhizomes of Boesenbergia pandurata showed potent preferential cytotoxicity against PANC-1 human pancreatic cancer cells under nutrient-deprived conditions, with a PC50 value of 6.6 µg/mL. Phytochemical investigation of this extract led to the isolation of 15 compounds, including eight new cyclohexene chalcones (1-8). The structures of the new compounds were elucidated by NMR spectroscopic data analysis. Among the isolated compounds obtained, isopanduratin A1 (14) and nicolaioidesin C (15) exhibited potent preferential cytotoxicity against PANC-1 human pancreatic cancer cells under nutrition-deprived conditions, with PC50 values of 1.0 and 0.84 µM, respectively.


Subject(s)
Antineoplastic Agents, Phytogenic/isolation & purification , Chalcone/isolation & purification , Chalcone/pharmacology , Chalcones/chemistry , Cyclohexanes/isolation & purification , Cyclohexanes/pharmacology , Pancreatic Neoplasms/drug therapy , Plant Extracts/chemistry , Rhizome/chemistry , Zingiberaceae/chemistry , Antineoplastic Agents, Phytogenic/chemistry , Antineoplastic Agents, Phytogenic/pharmacology , Cell Line, Tumor , Chalcone/chemistry , Chalcones/isolation & purification , Chalcones/pharmacology , Cyclohexanes/chemistry , Drug Screening Assays, Antitumor , Humans , Molecular Structure
6.
J Sep Sci ; 40(23): 4610-4618, 2017 Dec.
Article in English | MEDLINE | ID: mdl-28988464

ABSTRACT

Microwave- and ultrasound-assisted methods based on a quick, easy, cheap, effective, rugged, and safe sample preparation approach followed by high-performance liquid chromatography with tandem mass spectrometry were developed for the simultaneous determination of eight bisphenol analogues in serum and sediment. The developed methods provided satisfactory extraction efficiency for the energy provided by microwaves and ultrasound. Compositions of commercial sorbents (primary secondary amine, MgSO4 , octadecyl-modified silica, and graphitized carbon black) were evaluated. The ultrasound-assisted method was suited for serum using primary secondary amine, MgSO4 , and octadecyl-modified silica as sorbents and a mixture of hexane and ethyl acetate as extraction solvent. The microwave-assisted method worked better for sediment with tetrahydrofuran and methanol as solvents and primary secondary amine, MgSO4 , octadecyl-modified silica, and graphitized carbon black as sorbents. Other experimental parameters, such as extraction temperature and time, were also optimized. The inter- and intraday relative standard deviations ranged from 2.7 to 5.5%. The limits of detection were between 0.1 and 1.0 ng/mL for serum and between 0.1 and 0.5 ng/g dry weight for sediment. The proposed methods were successfully applied to seven sediment and 20 human serum samples. The results showed that the developed methods were practical for the analysis and biomonitoring of bisphenols in sera and sediment.


Subject(s)
Benzhydryl Compounds/blood , Benzhydryl Compounds/isolation & purification , Geologic Sediments/chemistry , Phenols/blood , Phenols/isolation & purification , Animals , Chromatography, High Pressure Liquid , Cyclohexanes/blood , Cyclohexanes/isolation & purification , Humans , Male , Microwaves , Rats, Sprague-Dawley , Solid Phase Extraction , Solvents , Sulfones/blood , Sulfones/isolation & purification , Tandem Mass Spectrometry , Ultrasonics
7.
J Asian Nat Prod Res ; 17(5): 550-8, 2015 May.
Article in English | MEDLINE | ID: mdl-26022116

ABSTRACT

Three new cyclohexenones (1-3, named sarcosones A-C) and two new isocoumarins (4 and 5), together with five known isocoumarins (6-10), were isolated from the solid cultures of an endophytic fungus Sarcosomataceae sp. NO.49-14-2-1. Their chemical structures were elucidated by analyses of HR-ESI-TOF-MS, (1)H, (13)C NMR, (1)H-(1)H COSY, HSQC, and HMBC spectra. Their absolute configurations were determined via modified Mosher's method and circular dichroism spectra method.


Subject(s)
Ascomycota/chemistry , Cyclohexanes/isolation & purification , Isocoumarins/isolation & purification , Cyclohexanes/chemistry , Isocoumarins/chemistry , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular
8.
J Org Chem ; 79(17): 7945-50, 2014 Sep 05.
Article in English | MEDLINE | ID: mdl-25101523

ABSTRACT

Investigation of the alkaloids from Myrioneuron faberi, a plant unique to China, gave four pairs of enantiomers (1-4). (±)-ß-Myrifabral A (1) and (±)-α-myrifabral A (2) formed an inseparable mixture of anomers (cluster A), as did (±)-ß-myrifabral B (3) and (±)-α-myrifabral B (4) (cluster B). Their structures were determined by X-ray diffraction and NMR analysis. Compounds 1-4 possessed novel cyclohexane-fused octahydroquinolizine skeletons and represent the first quinolizidine alkaloids from the genus Myrioneuron. The epimers of cluster A (1 and 2) were modified and separated. In vitro, clusters A and B and their derivatives inhibited replication of hepatitis C virus (HCV, IC50 0.9 to 4.7 µM) with cytotoxicity lower than that of telaprevir.


Subject(s)
Alkaloids/chemistry , Alkaloids/pharmacology , Antiviral Agents/chemistry , Antiviral Agents/pharmacology , Cyclohexanes/chemistry , Cyclohexanes/pharmacology , Hepacivirus/drug effects , Heterocyclic Compounds, 4 or More Rings/chemistry , Heterocyclic Compounds, 4 or More Rings/pharmacology , Quinolizines/chemistry , Quinolizines/pharmacology , Alkaloids/isolation & purification , Antiviral Agents/isolation & purification , Crystallography, X-Ray , Cyclohexanes/isolation & purification , Heterocyclic Compounds, 4 or More Rings/isolation & purification , Humans , Magnetic Resonance Spectroscopy , Molecular Structure , Quinolizines/isolation & purification , Stereoisomerism
9.
Environ Sci Technol ; 48(15): 8768-76, 2014.
Article in English | MEDLINE | ID: mdl-24955878

ABSTRACT

In this article, gas-phase advanced oxidation, a new method for pollution control building on the photo-oxidation and particle formation chemistry occurring in the atmosphere, is introduced and characterized. The process uses ozone and UV-C light to produce in situ radicals to oxidize pollution, generating particles that are removed by a filter; ozone is removed using a MnO2 honeycomb catalyst. This combination of in situ processes removes a wide range of pollutants with a comparatively low specific energy input. Two proof-of-concept devices were built to test and optimize the process. The laboratory prototype was built of standard ventilation duct and could treat up to 850 m(3)/h. A portable continuous-flow prototype built in an aluminum flight case was able to treat 46 m(3)/h. Removal efficiencies of >95% were observed for propane, cyclohexane, benzene, isoprene, aerosol particle mass, and ozone for concentrations in the range of 0.4-6 ppm and exposure times up to 0.5 min. The laboratory prototype generated a OH(•) concentration derived from propane reaction of (2.5 ± 0.3) × 10(10) cm(-3) at a specific energy input of 3 kJ/m(3), and the portable device generated (4.6 ± 0.4) × 10(9) cm(-3) at 10 kJ/m(3). Based on these results, in situ gas-phase advanced oxidation is a viable control strategy for most volatile organic compounds, specifically those with a OH(•) reaction rate higher than ca. 5 × 10(-13) cm(3)/s. Gas-phase advanced oxidation is able to remove compounds that react with OH and to control ozone and total particulate mass. Secondary pollution including formaldehyde and ultrafine particles might be generated, depending on the composition of the primary pollution.


Subject(s)
Air Pollution/prevention & control , Ozone/isolation & purification , Particulate Matter/isolation & purification , Photolysis , Volatile Organic Compounds/isolation & purification , Air Filters , Atmosphere/chemistry , Benzene/isolation & purification , Butadienes/isolation & purification , Cyclohexanes/isolation & purification , Environmental Pollution , Hazardous Substances/isolation & purification , Hemiterpenes/isolation & purification , Oxidation-Reduction , Pentanes/isolation & purification , Propane/isolation & purification , Ultraviolet Rays
10.
J Nat Prod ; 76(2): 297-301, 2013 Feb 22.
Article in English | MEDLINE | ID: mdl-23360521

ABSTRACT

A new chlorinated sesquiterpenoid analogue of fumagillin, ligerin (1), was isolated from a marine-derived strain of Penicillium, belonging to the subgenus Penicillium, along with the known compounds penicillic acid (2), orcinol, and orsellinic acid. Chemical structures were established by an interpretation of spectroscopic data including IR, UV, and HRESIMS, together with analyses of 1D and 2D NMR spectra and X-ray analysis for the determination of the absolute configuration. Ligerin (1) displayed strong inhibitory activity against an osteosarcoma cell line. This is the first report of the isolation of a fumagillin analogue from a marine-derived Penicillium strain.


Subject(s)
Antineoplastic Agents/isolation & purification , Antineoplastic Agents/pharmacology , Hydrocarbons, Chlorinated/isolation & purification , Hydrocarbons, Chlorinated/pharmacology , Penicillium/chemistry , Sesquiterpenes/isolation & purification , Sesquiterpenes/pharmacology , Antineoplastic Agents/chemistry , Cyclohexanes/chemistry , Cyclohexanes/isolation & purification , Drug Screening Assays, Antitumor , Estuaries , Fatty Acids, Unsaturated/chemistry , Fatty Acids, Unsaturated/isolation & purification , France , Hydrocarbons, Chlorinated/chemistry , Marine Biology , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Osteosarcoma/drug therapy , Penicillic Acid/isolation & purification , Sesquiterpenes/chemistry
11.
J Chem Ecol ; 37(4): 387-97, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21445566

ABSTRACT

Studies were conducted to develop an attractant for the cranberry weevil, Anthonomus musculus, a pest of blueberry and cranberry flower buds and flowers in the northeastern United States. In previous studies, we showed that cinnamyl alcohol, the most abundant blueberry floral volatile, and the green leaf volatiles (Z)-3-hexenyl acetate and hexyl acetate, emitted from both flowers and flower buds, elicit strong antennal responses from A. musculus. Here, we found that cinnamyl alcohol did not increase capture of A. musculus adults on yellow sticky traps compared with unbaited controls; however, weevils were highly attracted to traps baited with the Anthonomus eugenii Cano aggregation pheromone, indicating that these congeners share common pheromone components. To identify the A. musculus aggregation pheromone, headspace volatiles were collected from adults feeding on blueberry or cranberry flower buds and analyzed by gas chromatography-mass spectrometry. Three male-specific compounds were identified: (Z)-2-(3,3-dimethyl-cyclohexylidene) ethanol (Z grandlure II); (Z)-(3,3-dimethylcyclohexylidene) acetaldehyde (grandlure III); and (E)-(3,3- dimethylcyclohexylidene) acetaldehyde (grandlure IV). A fourth component, (E)-3,7-dimethyl-2,6-octadien-1-ol (geraniol), was emitted in similar quantities by males and females. The emission rates of these volatiles were about 2.8, 1.8, 1.3, and 0.9 ng/adult/d, respectively. Field experiments in highbush blueberry (New Jersey) and cranberry (Massachusetts) examined the attraction of A. musculus to traps baited with the male-produced compounds and geraniol presented alone and combined with (Z)-3-hexenyl acetate and hexyl acetate, and to traps baited with the pheromones of A. eugenii and A. grandis. In both states and crops, traps baited with the A. musculus male-produced compounds attracted the highest number of adults. Addition of the green leaf volatiles did not affect A. musculus attraction to its pheromone but skewed the sex ratio of the captured adults towards females. Although the role of plant volatiles in host-plant location by A. musculus is still unclear, our studies provide the first identification of the primary A. musculus aggregation pheromone components that can be used to monitor this pest in blueberry and cranberry pest management programs.


Subject(s)
Acetaldehyde/analogs & derivatives , Blueberry Plants/metabolism , Cyclohexanes/chemistry , Cyclohexanes/isolation & purification , Flowers/metabolism , Pheromones/analysis , Propanols/chemistry , Propanols/isolation & purification , Vaccinium macrocarpon/metabolism , Volatile Organic Compounds/analysis , Weevils/physiology , Acetaldehyde/chemistry , Acetaldehyde/isolation & purification , Acetates/chemistry , Acyclic Monoterpenes , Animals , Behavior, Animal/physiology , Cycloparaffins/chemistry , Cycloparaffins/isolation & purification , Female , Gas Chromatography-Mass Spectrometry , Male , New England , Terpenes/chemistry , Terpenes/isolation & purification
12.
Inorg Chem ; 49(23): 11164-73, 2010 Dec 06.
Article in English | MEDLINE | ID: mdl-20973558

ABSTRACT

A new CdL(2)-MOF was synthesized based on an asymmetric Schiff-base ligand LH, which is obtained by condensation of 5-formyl-8-hydroxyquinoline and 3-pyridinecarboxylic acid hydrazide. A series of organic six-membered ring analogues, namely, 1,4-dioxane, cyclohexane, cyclohexene, benzene, cyclohexanone, and cyclohexanol, can be absorbed by the CdL(2) porous framework in liquid-phase to generate G(n)⊂CdL(2) (n = 1 and 2) host-guest complexes. In addition, the CdL(2) host framework displays different affinity for these six-membered ring substrates and can effectively separate them under mild conditions (i.e., 1, 4-dioxane > cyclohexane > cyclohexene and benzene > cyclohexanone > cyclohexanol). The empty CdL(2) displays strong green-yellow emission. Furthermore, these host-guest systems show an interesting guest-driven luminescent emission, and the emission intensities of these guest-loaded complexes are effectively reduced.


Subject(s)
Benzene/isolation & purification , Cadmium Compounds/chemistry , Cyclohexanes/isolation & purification , Cyclohexanols/isolation & purification , Dioxanes/isolation & purification , Organometallic Compounds/chemistry , Adsorption , Cadmium Compounds/chemical synthesis , Cyclohexanones/isolation & purification , Models, Molecular , Organometallic Compounds/chemical synthesis , Schiff Bases/chemical synthesis , Schiff Bases/chemistry
13.
J Nat Prod ; 72(2): 265-9, 2009 Feb 27.
Article in English | MEDLINE | ID: mdl-19193024

ABSTRACT

Seven structurally related new polyoxygenated methyl cyclohexanoids, ampelomins A-G (1-7), were isolated from the mycelial solid culture of a soil-derived Ampelomyces fungus. Their structures were determined by spectroscopic and chemical means. Ampelomins A (1), C (3), E (5), and G (7) exhibited weak activity against alpha-glucosidase with IC(50) values of 1.74-5.93 mM, and ampelomin A (1) showed moderate antibacterial activity with MIC(90) values ranging from 202.4 to 1015.9 microM. A plausible polyketide biogenetic pathway is postulated for these compounds.


Subject(s)
Anti-Bacterial Agents/isolation & purification , Ascomycota/chemistry , Cyclohexanes/isolation & purification , Glycoside Hydrolase Inhibitors , Oxygen/chemistry , Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/pharmacology , Cyclohexanes/chemistry , Cyclohexanes/pharmacology , Escherichia coli/drug effects , Microbial Sensitivity Tests , Molecular Structure , Multienzyme Complexes/antagonists & inhibitors , Nuclear Magnetic Resonance, Biomolecular , Penicillium/enzymology , Proteus vulgaris/drug effects , Prunus/enzymology , Pseudomonas aeruginosa/drug effects , Saccharomyces cerevisiae/enzymology , Staphylococcus aureus/drug effects , beta-Glucosidase/antagonists & inhibitors
14.
J Asian Nat Prod Res ; 11(6): 523-8, 2009 Jun.
Article in English | MEDLINE | ID: mdl-20183285

ABSTRACT

Two new cyclohexyl-ethanol derivatives, incarvmareins A (1) and B (2), together with two known derivatives, 3 and 4, were isolated from the ethanolic extract of the roots of Incarvillea mairei. The structures of the new compounds were elucidated primarily on the basis of analysis of spectroscopic data.


Subject(s)
Bignoniaceae/chemistry , Cyclohexanes/isolation & purification , Drugs, Chinese Herbal/isolation & purification , Cyclohexanes/chemistry , Drugs, Chinese Herbal/chemistry , Ethanol/analogs & derivatives , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Plant Roots/chemistry
15.
Fitoterapia ; 134: 372-377, 2019 Apr.
Article in English | MEDLINE | ID: mdl-30878292

ABSTRACT

Eight new bisabolane derivatives, trichobisabolins A-H, along with two known ones, (3R,6R,7R)-1,10-bisaboladien-3-ol (9) and (3R,6R,7S)-1,10-bisaboladien-3,6-diol (10) were isolated from the culture of Trichoderma asperellum Y6-2, obtained from the surface of the marine red alga Chondrus ocellatus. Their structures and relative configurations were identified by interpretation of 1D/2D NMR and MS data. Compounds 1-8 were assayed for inhibiting the growth of some marine-derived organisms, including four marine phytoplankton species, one marine zooplankton species, and five pathogenic bacteria. All of them exhibited inhibition against the marine phytoplanktons with IC50 values ranging from 2.1-78 µg/mL, compounds 4 and 8 showed weak lethality to the marine zooplankton, and none of them had inhibition against the five pathogenic bacteria.


Subject(s)
Bacteria/drug effects , Chondrus/microbiology , Cyclohexanes/pharmacology , Phytoplankton/drug effects , Trichoderma/chemistry , China , Cyclohexanes/isolation & purification , Molecular Structure , Structure-Activity Relationship
16.
Nutrients ; 10(3)2018 Mar 20.
Article in English | MEDLINE | ID: mdl-29558444

ABSTRACT

Hyperglycemia occurs during diabetes and insulin resistance. It causes oxidative stress by increasing reactive oxygen species (ROS) levels, leading to cellular damage. Polyphenols play a central role in defense against oxidative stress. In our study, we investigated the antioxidant properties of simmondsin, a pure molecule present in jojoba seeds, and of the aqueous extract of jojoba seeds on fructose-induced oxidative stress in RINm5f beta cells. The exposure of RINm5f beta cells to fructose triggered the loss of cell viability (-48%, p < 0.001) and disruption of insulin secretion (p < 0.001) associated with of reactive oxygen species (ROS) production and a modulation of pro-oxidant and antioxidant signaling pathway. Cell pre-treatments with extracts considerably increased cell viability (+86% p < 0.001) for simmondsin and +74% (p < 0.001) for aqueous extract and insulin secretion. The extracts also markedly decreased ROS (-69% (p < 0.001) for simmondsin and -59% (p < 0.001) for aqueous extract) and caspase-3 activation and improved antioxidant defense, inhibiting p22phox and increasing nuclear factor (erythroid-derived 2)-like 2 (Nrf2) levels (+70%, p < 0.001) for aqueous extract. Simmondsin had no impact on Nrf2 levels. The richness and diversity of molecules present in jojoba seed extract makes jojoba a powerful agent to prevent the destruction of RINm5f beta cells induced by hyperglycemia.


Subject(s)
Acetonitriles/pharmacology , Antioxidants/pharmacology , Cyclohexanes/pharmacology , Fructose/toxicity , Glucosides/pharmacology , Insulin-Secreting Cells/drug effects , Magnoliopsida , Oxidative Stress/drug effects , Plant Extracts/pharmacology , Seeds , Acetonitriles/isolation & purification , Animals , Antioxidants/isolation & purification , Caspase 3/metabolism , Cell Line, Tumor , Cell Survival/drug effects , Cyclohexanes/isolation & purification , Dose-Response Relationship, Drug , Glucosides/isolation & purification , Insulin/metabolism , Insulin Secretion , Insulin-Secreting Cells/metabolism , Insulin-Secreting Cells/pathology , Magnoliopsida/chemistry , NADPH Oxidases/metabolism , NF-E2-Related Factor 2/metabolism , Phytotherapy , Plant Extracts/isolation & purification , Plants, Medicinal , Rats , Reactive Oxygen Species/metabolism , Seeds/chemistry , Signal Transduction/drug effects
17.
Phytochemistry ; 68(11): 1579-86, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17493646

ABSTRACT

Methanol extracts of Kaempferia rotunda L. rhizomes yielded seven compounds including six polyoxygenated cyclohexane derivatives identified as (-)-6-acetylzeylenol (1), four acylated derivatives of 1-benzoyloxymethyl-1,6-epoxycyclohexan-2,3,4,5-tetrol (3-6), a Diels-Alder adduct of 3-benzoyl-1-benzoyloxymethylcyclohexa-4,6-dien-2,3-diol (7), and a triacylated derivative of salicin (9). The cyclohexane diepoxide, crotepoxide (8), was also obtained. Spectroscopic methods were used for structure determination. The methanol extract of the rhizomes of K. rotunda and (-)-2-acetyl-4-benzoyl-1-benzoyloxymethyl-1,6-epoxycyclohexan-2,3,4,5-tetrol (2-acetylrotepoxide B; 6), had antifeedant activity against larvae of Spodoptera littoralis. (-)-Zeylenol (2) also showed antifeedant activity, whereas (-)-6-acetylzeylenol (1) was inactive.


Subject(s)
Cyclohexanes/chemistry , Zingiberaceae/chemistry , Animals , Benzyl Alcohols/chemistry , Benzyl Alcohols/isolation & purification , Benzyl Alcohols/pharmacology , Cyclohexanes/isolation & purification , Cyclohexanes/pharmacology , Feeding Behavior/drug effects , Glucosides , Larva/physiology , Plant Extracts/chemistry , Rhizome/chemistry , Spodoptera/physiology
18.
Water Res ; 41(6): 1343-9, 2007 Mar.
Article in English | MEDLINE | ID: mdl-17267009

ABSTRACT

Mixtures of anionic and cationic surfactants exhibit synergistic behavior as evidenced by low critical micelle concentrations (CMC) of the mixed system, increased surface activity, and improved detergency performance. The adsorption of a single-head anionic surfactant, sodium dodecyl sulfate (SDS), in mixture with a twin-head cationic surfactant, pentamethyl-octadecyl-1,3-propane diammonium dichloride (PODD), showed synergism of adsorption onto silica when present at a mixing ratio of 1:3 (cationic-rich), and also demonstrated lower surfactant desorption with water flushing of columns packed with the surfactant-modified media. In addition, the proportion of the mixed surfactants in the admicelles moved from the initial ratio of 1:3 towards equimolar after rinsing the surfactant-modified silica absorbent. The retardation of organic solutes passing through columns packed with modified-silica adsorbent increased nominally three fold for silica modified with mixed surfactants versus single surfactants (retardation factors increase from 4.0 to 12.8 for styrene and from 32.1 to 90.2 for ethylcyclohexane for single and mixed surfactants, respectively). Thus, this study demonstrates that mixed surfactant systems more effectively modified the silica surface than single surfactant systems both in terms of enhanced retardation of organic solutes and in terms of reduced surfactant desorption.


Subject(s)
Micelles , Surface-Active Agents/chemistry , Adsorption , Alkanes/chemistry , Chromatography/methods , Cyclohexanes/isolation & purification , Silicon Dioxide/chemistry , Sodium Dodecyl Sulfate/chemistry , Solubility , Styrene/isolation & purification , Water Pollution, Chemical/prevention & control
19.
Chemosphere ; 176: 97-107, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28260660

ABSTRACT

The removal of cyclohexane from gaseous emissions was studied using a biotrickling filter packed with polyurethane foam. Acivodorax sp. CHX100 was chosen as inoculum due to its ability to use cyclohexane as carbon source. Performance was evaluated by means of different resident times from 18 s to 37 s and concentration levels of 60, 90, 120, 160, 320, 480 and 720 mg C m-3, respectively. Removal efficiencies of 80%-99% and elimination capacities in the range of 5.4 g C m-3 h-1-38 g C m-3 h-1 were achieved for concentrations among 60 mg C m-3-480 mg C m-3. The removal efficiency decreased to 40% at concentrations of cyclohexane of 720 mg C m-3. The dynamics of the microbial population showed the strain CHX100 as predominant during the different operational process of biotrickling filter. The results of this study propose a novel approach for cleaning waste air containing cyclohexane by means of a biotrickling filter.


Subject(s)
Biodegradation, Environmental , Cyclohexanes/isolation & purification , Filtration/methods , Air Pollutants/chemistry , Air Pollutants/isolation & purification , Bioreactors , Gases/chemistry , Polyurethanes , Proteobacteria/metabolism
20.
J Plant Physiol ; 163(5): 557-61, 2006 Mar.
Article in English | MEDLINE | ID: mdl-16473660

ABSTRACT

In the current study, we investigated the influences of theobroxide on stem elongation in spinach (Spinacia oleracea). Our results showed that stem elongation and flower formation were inhibited by spraying spinach plants with theobroxide under inductive, long day conditions (16 h light/8 h dark), while application of exogenous applied GA3 prevented the effect of theobroxide. Quantitative analysis showed that theobroxide suppressed GA1 biosynthesis, whereas the endogenous content of jasmonic acid was unchanged. However, under short day conditions (10 h light/14 h dark), there were no differences in stem length between treated and untreated plants. These results suggest that the inhibition of stem elongation by theobroxide is probably due to the suppression of gibberellin biosynthesis.


Subject(s)
Cyclohexanes/pharmacology , Epoxy Compounds/pharmacology , Spinacia oleracea/drug effects , Spinacia oleracea/growth & development , Acetates/chemistry , Ascomycota/metabolism , Cyclohexanes/chemistry , Cyclohexanes/isolation & purification , Cyclopentanes/chemistry , Cyclopentanes/metabolism , Epoxy Compounds/chemistry , Epoxy Compounds/isolation & purification , Flowers/anatomy & histology , Flowers/drug effects , Flowers/growth & development , Gibberellins/biosynthesis , Gibberellins/pharmacology , Glucosides/chemistry , Light , Oxylipins , Plant Stems/anatomy & histology , Plant Stems/drug effects , Plant Stems/growth & development , Spinacia oleracea/anatomy & histology
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