Search results for "GAL"

showing 10 items of 9260 documents

Bioactive saponins with cancer related and immunomodulatory activity: Recent developments

2005

Abstract Saponins are natural glycosides of steroid or triterpene which exhibited many different biological and pharmacological actions: e.g. immunomodulatory, antitumor, antiinflammatory, molluscicidal, antiviral, antifungal, hypoglycemic, hypocholesterolemic, to mention just a few. The aim of this summarize recent advances on the bioactivity of saponins related to cancer and immune system, which has attracted a great attention during the last five years

chemistry.chemical_classificationAntifungalmedicine.drug_classmedicine.medical_treatmentGlycosideCancerPharmacologyBiologymedicine.diseaseSteroidImmune systemTriterpenechemistrymedicine
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Water-soluble polysaccharides from Opuntia stricta Haw. fruit peels: Recovery, identification and evaluation of their antioxidant activities

2015

Abstract Opuntia stricta Haw. is considered as one of the most common cactus plant growing in Tunisia. Extracting valuable compounds from its fruit peel, considered as by-product, is drawing more and more attention, making it on the verge of commercialization. Water-soluble polysaccharides were extracted from Opuntia stricta Haw. peels, and their chemical composition assessed using thin layer chromatography. The antioxidant activities of the extracted polysaccharides were assessed using 2,2-diphenyl-1-picrylhydrazyl free radical scavenging activity, total antioxidant activity and reducing power capacity. The extraction yield of water-soluble polysaccharides was 7.53±0.86%. The chemical comp…

chemistry.chemical_classificationArabinoseAntioxidant[SDV.BIO]Life Sciences [q-bio]/BiotechnologyRhamnoseOpuntia stricta Haw. peelsmedicine.medical_treatment[SDV]Life Sciences [q-bio]Extraction (chemistry)antioxidant activityPolysaccharideAscorbic acidThin-layer chromatographychemistry.chemical_compoundchemistrywater-soluble polysaccharidesGalactoseBotanymedicinepolysaccharide extraction[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process EngineeringFood science[SDV.AEN]Life Sciences [q-bio]/Food and Nutrition
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ERA-experiment “space biochemistry”

1995

Abstract The general goal of the experiment was to study the response of anhydrobiotic (metabolically dormant) microorganisms (spores of Bacillus subtilis, cells of Deinococcus radiodurans, conidia of Aspergillus species) and cellular constituents (plasmid DNA, proteins, purple membranes, amino acids, urea) to the extremely dehydrating conditions of open space, in some cases in combination with irradiation by solar UV-light. Methods of investigation included viability tests, analysis of DNA damages (strand breaks, DNA-protein cross-links) and analysis of chemical effects by spectroscopic, electrophoretic and chromatographic methods. The decrease in viability of the microorganisms was as exp…

chemistry.chemical_classificationAtmospheric SciencebiologyDNA damageChemistryMicroorganismFungal geneticsAerospace EngineeringAstronomy and AstrophysicsDeinococcus radioduransBacillus subtilisbiology.organism_classificationAmino acidchemistry.chemical_compoundGeophysicsBiochemistrySpace and Planetary ScienceUreaGeneral Earth and Planetary SciencesDNAAdvances in Space Research
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Synthesis of cyanoacetic acid by carbon dioxide and electrogenerated acetonitrile anion in undivided cells equipped with sacrificial anodes

2008

The electrochemical synthesis of cyanoacetic acid was performed by cathodic reduction of tetraalkylammonium salts (R4NX) in acetonitrile in undivided cells equipped with sacrificial anodes with concomitant or subsequent addition of carbon dioxide. These syntheses avoid the use of dangerous reagents, yield cyanoacetic acid in moderate faradic yields and confirm that the cathodic reduction of tetraalkylammonium salts in the presence of acetonitrile leads to the formation of the anion CNCH2-.

chemistry.chemical_classificationCHLOROACETONITRILE electrocarboxylationNitrileSupporting electrolyteGalvanic anodecathodic reduction of alkyl ammonium saltsGeneral Chemical EngineeringCarboxylic acidInorganic chemistrycarbon dioxideSettore ING-IND/27 - Chimica Industriale E TecnologicaElectrochemistryAnalytical Chemistrychemistry.chemical_compoundsupporting electrolyteSettore ING-IND/22 - Scienza E Tecnologia Dei Materialialkyl ammonium saltCyanoacetic acidchemistryReagentElectrochemistrycyanoacetic acidAcetonitrilesacrificial anodeJournal of Electroanalytical Chemistry
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Carbamate Linker Strategy in Solid-Phase Synthesis of Amino-Functionalized Glycoconjugates for Attachment to Solid Surfaces and Investigation of Prot…

2009

Amino-functionalized serine-based galactose and glucose neoglycolipids were prepared by solid-phase synthesis using a carbamate strategy for anchoring amino functionalities to a (2-fluoro-4-hydroxy ...

chemistry.chemical_classificationCarbamateGlycoconjugateSolid surfacemedicine.medical_treatmentOrganic ChemistrySerinechemistry.chemical_compoundSolid-phase synthesischemistryGalactosemedicineProtein–carbohydrate interactionsOrganic chemistryPhysical and Theoretical ChemistryLinkerEuropean Journal of Organic Chemistry
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A strategy for chromatographic and structural analysis of monosaccharide species from glycoproteins.

1996

A general strategy for the chromatographic and structural analysis of the monosaccharide species fucose (Fuc), N-acetylgalactosamine (GalNAc), N-acetylglucosamine (GlcNAc), galactose (Gal), glucose (Glc), mannose (Man), N-acetylneuraminic acid (NANA) present in glycoproteins is described. Qualitative and quantitative aspects for the separation of these glycoprotein monosaccharides (monosaccharide species) using ligand-exchange chromatography (LEC) and high pH anion-exchange chromatography (HPAEC) in combination with pulsed-amperometric detection (PAD), refractive index (RI) and ultraviolet (UV) monitoring are discussed in detail. The conditions for the acidic hydrolysis of glycoproteins and…

chemistry.chemical_classificationChemical ionizationGlycosylationChromatographyMolecular massChemistryMass spectrometryBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundBiochemistryLiquid chromatography–mass spectrometryGalactoseMonosaccharideAnalytical and bioanalytical chemistry
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Inhibition of cyclodextrins on α-galactosidase.

2017

This work successfully investigated the effects of different influential factors and hydrophobic cavities of cyclodextrins (CDs) on α-galactosidase (α-Gal) by detecting α-Gal activity. The highest inhibitory concentration of three kinds of CDs (α-, β-, and γ-CD) on α-Gal was 10mM. Moreover, the highest inhibition of α-Gal was obtained under the following conditions: reaction time of 90min, temperature of 30°C, and pH 6.0. Compared with other CDs, β-CD showed more ability to interact with α-Gal due to its appropriate cavity geometric dimensions. From circular dichroism and nuclear magnetic resonance it was observed that β-CD changed the secondary structure of α-Gal and formed a hydrogen bond…

chemistry.chemical_classificationCircular dichroismCyclodextrinsMagnetic Resonance Spectroscopy010405 organic chemistryChemistryHydrogen bondStereochemistryCircular DichroismTemperatureHydrogen BondingGeneral Medicine010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical ChemistryCrystallographyα galactosidaseEnzymealpha-GalactosidaseProtein secondary structureFood ScienceFood chemistry
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Role of hexagonal structure-forming lipids in diadinoxanthin and violaxanthin solubilization and de-epoxidation

2005

In this study, we have examined the influence of different lipids on the solubility of the xanthophyll cycle pigments diadinoxanthin (Ddx) and violaxanthin (Vx) and on the efficiency of Ddx and Vx de-epoxidation by the enzymes Vx de-epoxidase (VDE) from wheat and Ddx de-epoxidase (DDE) from the diatom Cyclotella meneghiniana, respectively. Our results show that the lipids MGDG and PE are able to solubilize both xanthophyll cycle pigments in an aqueous medium. Substrate solubilization is essential for de-epoxidase activity, because in the absence of MGDG or PE Ddx and Vx are present in an aggregated form, with limited accessibility for DDE and VDE. Our results also show that the hexagonal st…

chemistry.chemical_classificationDiatomsBilayerGalactolipidsPhosphatidylethanolaminesLipid BilayersHexagonal phaseDiadinoxanthinSubstrate (chemistry)BiologyXanthophyllsbeta CaroteneBiochemistrySubstrate Specificitychemistry.chemical_compoundEnzymeBiochemistrychemistrySolubilityXanthophyllThylakoidPhosphatidylcholinesOxidoreductasesViolaxanthin
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Synthesis of Trisaccharides by Hetero-Diels–Alder Welding of Two Monosaccharide Units

2012

A new strategy for the synthesis of di- and trisaccharides based on the de novo synthesis of the linking saccharide unit is presented. In this strategy, functionalized monosaccharide building blocks already incorporating the glycosidic linkages are welded together using a metal-catalyzed hetero-Diels–Alder (HDA) reaction to generate a new monosaccharide unit between them. The highest yields and selectivities in the HDA reaction were obtained by using chiral Schiff base chromium complexes. Disaccharide products were accessible by reaction of Danishefsky's diene with acetyl- and benzyl-protected galactoside aldehydes. For the synthesis of trisaccharide products, acetyl-protected glucose or ga…

chemistry.chemical_classificationDieneOrganic ChemistryDisaccharideGlycosidic bondGalactosideCycloadditionchemistry.chemical_compoundchemistryMonosaccharideOrganic chemistryStereoselectivityTrisaccharidePhysical and Theoretical Chemistryta116European Journal of Organic Chemistry
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Total Synthesis of a Partial Structure from Arabinogalactan and Its Application for Allergy Prevention

2020

Abstract Arabinogalactan, a microheterogeneous polysaccharide occurring in plants, is known for its allergy‐protective activity, which could potentially be used for preventive allergy treatment. New treatment options are highly desirable, especially in a preventive manner, due to the constant rise of atopic diseases worldwide. The structural origin of the allergy‐protective activity of arabinogalactan is, however, still unclear and isolation of the polysaccharide is not feasible for pharmaceutical applications due to a variation of the activity of the natural product and contaminations with endotoxins. Therefore, a pentasaccharide partial structure was selected for total synthesis and subse…

chemistry.chemical_classificationDrug Discovery | Hot PaperNatural productallergy protectionAllergy preventionCommunicationOrganic ChemistrycarbohydratesAirway inflammationTreatment optionsTotal synthesisGeneral Chemistryairway inflammationPolysaccharideCommunicationsCatalysisarabinogalactanchemistry.chemical_compoundchemistryBiochemistryArabinogalactanCarrier proteintotal synthesisChemistry – A European Journal
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