Search results for "Mechanism"

showing 10 items of 1835 documents

Editorial: Pathophysiologic Insights From Biomarker Studies in Neurological Disorders

2020

business.industryneurodegenerationneuroimmunologyBioinformaticslcsh:RC346-429PathophysiologyEditorialNeuroimmunologyNeurologybiomarkerBiomarker (medicine)MedicineNeurology (clinical)pathomechanismbusinesslcsh:Neurology. Diseases of the nervous systempathophysiologyFrontiers in Neurology
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Adipose stromal cells promote the transition of colorectal cancer cells toward a mesenchymal-like phenotype

2021

ABSTRACT Colon cancer progression is among the risks that increase with obesity. We have recently unveiled the molecular mechanism by which adipose tissue-released molecules, HGF and IL-6, make colorectal cancer (CRC) cells acquiring mesenchymal traits. Targeting of adipose-derived factors abrogate the metastatic potential of CRC stem cells (CR-CSCs) in obese patients.

cancer stem cellCancer ResearchStromal cellTransition (genetics)Colorectal cancerbusiness.industryadipose stromal cellMesenchymal stem cellAdipose tissuecolorectal cancermedicine.diseasePhenotypedigestive system diseaseshybrid EMTCommentaryMolecular mechanismCancer researchmedicineMolecular MedicineSettore MED/46 - Scienze Tecniche Di Medicina Di LaboratorioStem cellbusinessobesity.Article CommentaryMolecular & Cellular Oncology
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Quadruply-bonded dimolybdenum compounds: Reactivity towards TCNE. Structural evidences for the 1-D polymer [Mo2(O2 CCF3)4(TCNE)]∞

2005

cited By 3; International audience; Reaction of [Mo2(O2CR)4] (R = CF 3, 1) with TCNE in toluene affords the new compound [Mo2(O2CCF3)4 (TCNE)·6H5CH3 (2). The structure of 2 is built on [Mo2(O2 CCF3)4] fragments having the usual paddlewheel structure of 1 (Mo-Mo 2.1117(8) Å) and TCNE units. Each polynitrile moiety acts as a bridging ligand between two Mo2 fragments (Mo-N 2.875(4) Å) affording 1-D polymeric chains crossing in the crystal; the toluene molecules occupy the cavities between the chains. 13C NMR, IR and electrochemical data clearly show that formation of 2 does not involve electron density transfer from dimolybdenum fragment to the TCNE unit, which remains in 2 in its neutral stat…

chemical reactionReaction mechanismStereochemistryCoordination polymerGeneral Chemical EngineeringpolymerCrystal structureTetracyanoethylene010402 general chemistryligand01 natural scienceschemistry.chemical_compoundmolybdenumelectrochemical analysisMoietyMoleculetoluene[CHIM]Chemical SciencesReactivity (chemistry)electron transportchemical bondinfrared spectroscopychemical binding010405 organic chemistryChemistryarticleBridging ligandGeneral Chemistrycarbon nuclear magnetic resonance0104 chemical sciencesCrystallographychemical analysispolymerizationchemical structureorganometallic compound
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The mechanism of formation of 3H,9H-Pyrano[3,4-b]indol-3-ones from 3-indolalkanoic acids

1991

The mechanism of the formation of 1-methyl-3H,9H-pyrano[3,4-b]indol-3-one (4) from the corresponding 3-indolacetic acid 1 is discussed. The suggested mechanism is substantiated by the isolation of a stable intermediate 2 and its transformations in the presence of acetic anhydride and/or Lewis acids.

chemistry.chemical_classificationAcetic anhydridechemistry.chemical_compoundReaction mechanismchemistryStereochemistryCarboxylic acidOrganic ChemistryLewis acids and basesPhysical and Theoretical ChemistryLactoneMechanism (sociology)Liebigs Annalen der Chemie
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A synthetic hexapeptide (Argireline) with antiwrinkle activity

2008

Botulinum neurotoxins (BoNTs) represent a revolution in cosmetic science because of their remarkable and long-lasting antiwrinkle activity. However, their high neurotoxicity seriously limits their use. Thus, there is a need to design and validate non-toxic molecules that mimic the action of BoNTs. The hexapeptide Ac-EEMQRR-NH2 (coined Argireline) was identified as a result of a rational design programme. Noteworthy, skin topography analysis of an oil/water (O/W) emulsion containing 10% of the hexapeptide on healthy women volunteers reduced wrinkle depth up to 30% upon 30 days treatment. Analysis of the mechanism of action showed that Argireline significantly inhibited neurotransmitter relea…

chemistry.chemical_classificationAgingRational designNeurotoxicityPharmaceutical SciencePeptideDermatologymedicine.diseaseExocytosisColloid and Surface ChemistryMechanism of actionchemistryBiochemistryChemistry (miscellaneous)In vivoDrug DiscoveryToxicitymedicineNeurotoxinmedicine.symptomInternational Journal of Cosmetic Science
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Reactions of α-diimino ligands with the chloro-bridged dimer [RhCl(COD)]2(COD=1,5-cyclooctadiene)

1988

Abstract The reactions of α-diimino ligands N - N ′ [ N - N ′= 2,2′-bipyridine (bipy), C 5 H 4 N2CHNR (R= C 6 H 4 OMe- p , PyCa), RNCHCHNR (R=C 6 H 4 - OMe- p , DAB)] with [RhCl(COD)] 2 give rise to stoichiometry, solvent, ligand, and temperature dependent equilibria. In general, the 1/1 ligand/dimer reaction yields the ionic product [Rh(COD)( N - N ′)] [RhCl 2 (COD)], at room temperature. For N - N ′=DAB, the ionic form is in equilibrium with the binuclear compound [{RhCl(COD)} (μ-DAB){RhCl(COD)}] (containing a σ σ,'- N , N ′ bridging α-diimine), which becomes the predominant species at low temperatures. In [Rh(COD)( N - N ′)] [RhCl 2 (COD)], a fast exchange of the Rh(COD) unit betwe…

chemistry.chemical_classificationAldimineReaction mechanismDenticityStereochemistryLigandDimer15-CyclooctadieneCationic polymerizationMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundchemistryMaterials ChemistryPhysical and Theoretical ChemistryIsomerizationInorganica Chimica Acta
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Selective access to either a doubly boron-doped tetrabenzopentacene or an oxadiborepin from the same precursor

2019

Depending on the solvent, a brominated arylborane gave the multiple helicene B2-TBPA (pyridine) or the oxadiborepin ODBE (THF) after intramolecular Yamamoto coupling.

chemistry.chemical_classificationAnthraceneReaction mechanism010405 organic chemistrychemistry.chemical_elementGeneral ChemistryElectron acceptor010402 general chemistry01 natural sciences0104 chemical sciencesChemistrychemistry.chemical_compoundCrystallographychemistryIntramolecular forceYield (chemistry)PyridineMoietyBoronChemical Science
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The enzymatic mechanism of epoxide hydrolysis

1995

chemistry.chemical_classificationCancer Researchchemistry.chemical_compoundHydrolysisEnzymeOncologyBiochemistryMechanism (biology)ChemistryEnzymatic hydrolysisEpoxideGeneral MedicineJournal of Cancer Research and Clinical Oncology
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Sequiterpene-related compounds as endocrine disrupters in Oncopeltus fasciatus, and potential reduced glutathione synthesis modifiers

1999

Sesquiterpene lactones have been found to exhibit effects on insect growth and development. In this study, the bioactivity of natural lactones extracted from Centaurea mariolensis and some structurally related synthetic derivatives has been investigated. Assays have also been carried out in order to determine the potential of these lactones as modifiers of reduced glutathione (GSH) synthesis.

chemistry.chemical_classificationEnvironmental EngineeringChemical compoundStereochemistryChemical structureBiological activityGlutathioneBiologySesquiterpenePollutionchemistry.chemical_compoundMechanism of actionchemistryBiochemistryEndocrine disruptormedicineEnvironmental Chemistrymedicine.symptomWaste Management and DisposalLactoneScience of The Total Environment
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The Catalytic Mechanism of Carboxylesterases: A Computational Study

2014

The catalytic mechanism of carboxylesterases (CEs, EC 3.1.1.1) is explored by computational means. CEs hydrolyze ester, amide, and carbamate bonds found in xenobiotics and endobiotics. They can also perform transesterification, a reaction important, for instance, in cholesterol homeostasis. The catalytic mechanisms with three different substrates (ester, thioester, and amide) have been established at the M06-2X/6-311++G**//B3LYP/6-31G* level of theory. It was found that the reactions proceed through a mechanism involving four steps instead of two as is generally proposed: (i) nucleophilic attack of serine to the substrate, forming the first tetrahedral intermediate, (ii) formation of the ac…

chemistry.chemical_classificationEsterificationStereochemistrycomputational studiesHydrolysisSubstrate (chemistry)AlcoholTransesterificationcatalytic mechanismCrystallography X-RayThioesterBiochemistryCatalysischemistry.chemical_compoundcarboxylesterasesNucleophilechemistryhydrolysisTetrahedral carbonyl addition compoundAmideBiocatalysisCarboxylic Ester Hydrolases
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