Search results for "RATES"

showing 10 items of 1636 documents

Crystallization kinetics in relation to polymer processing

1993

Phase distribution of quenched samples has been determined by a deconvolution procedure of WAXS spectra in a wide range of cooling rates. The informations collected together with isothermal and DSC results provide a very wide set of data on the crystallization kinetics of polymers relevant which covers conditions encountered in most polymer processing operations. They have been compared with predictions of a non-isothermal crystallization model assuming two independent and parallel crystallization processes competing during solidification.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryThermodynamicsCooling ratesPolymerCondensed Matter PhysicsIsothermal processSpectral linelaw.inventionCrystallization kineticsCrystallographychemistrylawPhase (matter)Materials ChemistryDeconvolutionCrystallizationMakromolekulare Chemie. Macromolecular Symposia
researchProduct

Chitin: A Structural Biopolysaccharide

2009

Chitin is a naturally occurring fibre-forming polymer that plays a protective role in many lower eukaryotes similar to that of cellulose in plants. Chemically it is a long-chain unbranched polysaccharide made of N-acetylglucosamine residues; it is the second most abundant organic compound in nature, after cellulose. Taking into account the structural role played by chitin, its metabolism (synthesis and degradation) is essential for different morphogenetic events. Absent in vertebrates and plants, chitin represents a parasite-specific target for chemotherapeutic attack and also plays a role in host immune responses. Because of its abundance in nature and its properties, biotechnological appl…

chemistry.chemical_classificationMaterials sciencebiologyCuticlefungimacromolecular substancesChitin synthasePolysaccharidecarbohydrates (lipids)ChitosanCell wallchemistry.chemical_compoundchemistryBiochemistryChitinChitinasebiology.proteinChitin nanofibrileLS
researchProduct

Molecular aggregation in selected crystalline 1:1 complexes of hydrophobicD- andL-amino acids. IV. TheL-phenylalanine series

2009

The amino acid L-phenylalanine has been cocrystallized with D-2-aminobutyric acid, C(9)H(11)NO(2).C(4)H(9)NO(2), D-norvaline, C(9)H(11)NO(2).C(5)H(11)NO(2), and D-methionine, C(9)H(11)NO(2).C(5)H(11)NO(2)S, with linear side chains, as well as with D-leucine, C(9)H(11)NO(2).C(6)H(13)NO(2), D-isoleucine, C(9)H(11)NO(2).C(6)H(13)NO(2), and D-allo-isoleucine, C(9)H(11)NO(2).C(6)H(13)NO(2), with branched side chains. The structures of these 1:1 complexes fall into two classes based on the observed hydrogen-bonding pattern. From a comparison with other L:D complexes involving hydrophobic amino acids and regular racemates, it is shown that the structure-directing properties of phenylalanine closel…

chemistry.chemical_classificationMolecular StructureChemistryStereochemistryAminobutyratesPhenylalanineHydrogen BondingStereoisomerismStereoisomerismPhenylalanineGeneral MedicineCrystallography X-RayGeneral Biochemistry Genetics and Molecular BiologyAmino acidValineSide chainIsoleucineLeucineAminobutyratesHydrophobic and Hydrophilic InteractionsActa Crystallographica Section C Crystal Structure Communications
researchProduct

Synthetic Tumor-Associated Glycopeptide Antigens from the Tandem Repeat Sequence of the Epithelial Mucin MUC4

2004

In cancer research, the development of vaccines against tumor-associated antigens is of particular interest. Epithelial cells express mucin type glycoproteins, which are extensively O-glycosylated. In case of cancer, the expression of these mucins is increased, and their carbohydrate side chains show an aberrant glycosylation pattern. A set of single and double glycosylated hexadecapeptides representing the tandem repeat sequence of the epithelial mucin MUC4 carrying different tumor-associated carbohydrate antigens was prepared by sequential solid-phase glycopeptide synthesis. The crucial glycosyl amino acid building blocks containing the T N , T, sialyl-T N and (2,6)-sialyl-T antigens were…

chemistry.chemical_classificationOrganic ChemistryMucinGeneral MedicineMolecular biologyCatalysisGlycopeptideAmino acidcarbohydrates (lipids)chemistry.chemical_compoundSolid-phase synthesisAntigenchemistryBiochemistryGalactosamineGlycosylThreonineGlycoproteinSynthesis
researchProduct

Does catalase play a role in Adriamycin induced cardiotoxicity?

1980

Summary Adriamycin causes an increase of lipid peroxidation in mouse cardiac homogenates that is dependent on the concentration of the antiblastic. The same phenomenon is not observed in the hearts of mice treated with an elevated dose of Adriamycin in which, conversely, an increase of the antioxidizing enzyme catalase was noticed. The significance of these findings is discussed with relationship to the hypothesis of an enhanced free radicals formation at the basis of Adriamycin induced cardiotoxicity.

chemistry.chemical_classificationPharmacologyCardiotoxicityLipid PeroxidesbiologyFree RadicalsHeart DiseasesMyocardiumPharmacologyNADCatalaseMalonatescarbohydrates (lipids)Lipid peroxidationchemistry.chemical_compoundMiceEnzymechemistryCatalaseDoxorubicinMalondialdehydepolycyclic compoundsbiology.proteinAnimalsFemalePharmacological Research Communications
researchProduct

Behavior of carbohydrate-based material in black liquor during heating

2004

One industrial softwood Kraft black liquor was heat-treated (at 175 ?C and 190 ?C for 15-60 min) together with laboratory-made soda-AQ (wheat straw and reed canary grass) and Kraft (reed canary grass) black liquors (at 190 ?C for 30 min). The feedstock black liquors were characterized with respect to their polysaccharide (mainly xylem) and aliphatic carboxylic acid contents before and after the heat treatments. It was noted that, due to the higher amount of polysaccharides in the non-wood black liquors (8.2-16.6% of d.s) compared to that in the softwood black liquor (1.4% of d.s), the heat treatment in the former case resulted in a 5-30% increase in the amount of aliphatic acids formed by v…

chemistry.chemical_classificationSoftwoodbiologyheat treatmentRenewable Energy Sustainability and the EnvironmentChemistrylcsh:Mechanical engineering and machineryCarboxylic acidaliphatic carboxylic acidspolysaccharidescarbohydratesfood and beveragesblack liquorRaw materialStrawequipment and suppliesbiology.organism_classificationPolysaccharidePulp and paper industrylcsh:TJ1-1570non-woodCanary grassBlack liquorKraft paperwoodThermal Science
researchProduct

Differential function of the phosphoglucomutase isozymes PGM1 and PGM2

1979

A total of 13 metabolites thought to be possibly inhibitory were tested for their influence on PGM isozyme activities, each at several different concentrations. The analysis of statistical significance was based on enzyme activities obtained by densitometric measurements of starch gels. Five of the substances were found to inhibit PGM activity, three of which definitely and a further one probably led to a significantly stronger inhibition of the isozymes of the PGM2 locus than of PGM1 isozymes. They are (1) fructose-1,6-diphosphate, (2) adenosine triphosphate, (3) citrate, and (4) possibly 2,3-diphosphoglycerate. Thus, PGM1 isozymes proved to function better in hard or perhaps marginal meta…

chemistry.chemical_classificationStarchChromosome MappingLocus (genetics)BiologyDiphosphoglyceric AcidsMolecular biologyIsozymeIsoenzymeschemistry.chemical_compoundAdenosine TriphosphateEnzymeGenesPhosphoglucomutasechemistryBiochemistryPGM1FructosediphosphatesGeneticsHumansPhosphoglucomutaseCitratesAdenosine triphosphateGeneGenetics (clinical)Human Genetics
researchProduct

Capillary column gas chromatographic identification of sugars in honey as trimethylsilyl derivatives.

1987

A method for identifying carbohydrates (mono-, di- and trisaccharides) in honey is presented. It is based on the separate preparation of both trimethylsilyl ethers and oxime trimethylsilyl ethers of the sugars followed by their gas chromatographic separation on a fused-silica capillary column coated with OV-101 using temperature programming. From the two chromatograms, the number of peaks given by each derivatized sugar, their relative retention times and peak-area ratios are used for identification. The identities of two unidentified trisaccharide peaks are considered. Quantitative applications to honey sugar analysis are discussed.

chemistry.chemical_classificationTrimethylsilyl CompoundsChromatographyChromatography GasTrimethylsilylOrganic ChemistryCarbohydratesTemperatureGeneral MedicineHoneyCarbohydrateOximeBiochemistryAnalytical Chemistrychemistry.chemical_compoundChromatographic separationchemistryCapillary columnOximesOrganic chemistryIndicators and ReagentsTrisaccharideGas chromatographySugarJournal of chromatography
researchProduct

Synthetic Glycopeptides of the Tandem Repeat Sequence of the Epithelial Mucin MUC4 with Tumour-associated Carbohydrate Antigens

2004

Glycohexadecapeptides representing the tandem repeat sequence of the epithelial mucin MUC4 were prepared by applying a solid-phase methodology. The required glycosyl amino acid building blocks containing the tumour-associated saccharide antigens T N -, T,- sialyl-T N , (2,6)- and (2,3)-sialyl-T were synthesized according to a straightforward biomimetic strategy by stepwise extension of the saccharide side chain of a Fmoc-protected galactosamine threonine tert-butyl ester.

chemistry.chemical_classificationTumor-Associated Carbohydrate AntigensChemistryOrganic ChemistryMucinGeneral MedicineMolecular biologyGlycopeptideAmino acidcarbohydrates (lipids)chemistry.chemical_compoundAntigenBiochemistryGalactosamineTandem Repeat SequenceSide chainGlycosylThreonineSynlett
researchProduct

ChemInform Abstract: Oligosaccharide Synthesis via Electrophile-Induced Activation of Glycosyl-N-allylcarbamates.

2010

Abstract Glycosyl-N-allyl carbamates, obtained by reaction of anomerically unprotected saccharides with allyl isocyanate, can be activated by an electrophile-induced cyclisation and reacted with glycosyl acceptors to form the corresponding oligosaccharides By this method the mucin core 2 trisaccharide2 has successfully been synthesized. Due to the mild glycosylation conditions even 1-O-acetyl protected glycosyl acceptors can be used. This was demonstrated in the synthesis of a 1,6-linked glucosyl trisaccharide whereby a reptitious glycosylation strategy could be applied. 1. Dedicated to the memory of Professor Akira Hasegawa.

chemistry.chemical_classificationanimal structuresGlycosylationStereochemistryMucinfood and beveragesmacromolecular substancesGeneral Medicinecarbohydrates (lipids)chemistry.chemical_compoundchemistryElectrophilelipids (amino acids peptides and proteins)GlycosylTrisaccharideAllyl isocyanateOligosaccharide synthesisChemInform
researchProduct