Search results for " Synthesis"

showing 10 items of 1625 documents

Heterometallic Titanium–Organic Frameworks by Metal-Induced Dynamic Topological Transformations

2020

Reticular chemistry has boosted the design of thousands of metal and covalent organic frameworks for unlimited chemical compositions, structures, and sizable porosities. The ability to generate porous materials at will on the basis of geometrical design concepts is responsible for the rapid growth of the field and the increasing number of applications derived. Despite their promising features, the synthesis of targeted homo- and heterometallic titanium–organic frameworks amenable to these principles is relentlessly limited by the high reactivity of this metal in solution that impedes the controlled assembly of titanium molecular clusters. We describe an unprecedented methodology for the syn…

Solvothermal synthesischemistry.chemical_elementGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical sciencesMetalCrystalColloid and Surface ChemistrychemistryTransition metalChemical engineeringvisual_artvisual_art.visual_art_mediumSBusIsostructuralMesoporous materialTitaniumJournal of the American Chemical Society
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FINDUS: An Open-Source 3D Printable Liquid-Handling Workstation for Laboratory Automation in Life Sciences

2020

3D-printed laboratory devices can enable ambitious research purposes even at a low-budget level. To follow this trend, here we describe the construction, calibration, and usage of the FINDUS (Fully Integrable Noncommercial Dispensing Utility System). We report the successful 3D printing and assembly of a liquid-handling workstation for less than $400. Using this setup, we achieve reliable and flexible liquid-dispensing automation with relative pipetting errors of less than 0.3%. We show our system is well suited for several showcase applications from both the biology and chemistry fields. In support of the open-source spirit, we make all 3D models, assembly instructions, and source code ava…

Source codeWorkstationComputer sciencemedia_common.quotation_subject3D printingcomputer.software_genre01 natural sciencesBiological Science DisciplinesCathepsin Blaw.invention03 medical and health scienceslawArduinoHumansSolid-Phase Synthesis Techniques030304 developmental biologymedia_commoncomputer.programming_languageAutomation Laboratory0303 health sciences010405 organic chemistrybusiness.industryPython (programming language)Automation0104 chemical sciencesComputer Science ApplicationsMedical Laboratory TechnologyOpen sourceCalibrationPrinting Three-DimensionalLaboratory automationOperating systemPeptidesbusinesscomputerSoftwareSLAS Technology
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Guanaconetins, new antitumoral acetogenins, mitochondrial complex I and tumor cell growth inhibitors

2005

The antitumoral activity of a series of acetylated bis-tetrahydrofuranic acetogenins with a threo/trans/threo/trans/erythro relative configuration was characterized by four new natural and two semisynthetic, 15,24,30-trioxygenated acetogenins that were found to inhibit mitochondrial complex I enzyme as well as growth of several tumor cell lines. Placement of acetyl groups along the alkyl chain modulated the potency of the bis-tetrahydrofuranic acetogenins and could be important for future utilization of these compounds as chemotherapeutic agents.

Spectrometry Mass Electrospray IonizationMagnetic Resonance SpectroscopyAcetogeninsStereochemistryClinical BiochemistryPharmaceutical ScienceAntineoplastic AgentsBiochemistryChemical synthesisLactonesStructure-Activity Relationshipchemistry.chemical_compoundCell Line TumorNeoplasmsDrug DiscoveryHumansStructure–activity relationshipMolecular BiologyCell Proliferationchemistry.chemical_classificationElectron Transport Complex IMolecular StructureChemistryCell growthOrganic ChemistryBiological activityGrowth InhibitorsEnzymeBiochemistryAcetylationCell cultureAcetogeninMolecular MedicineFatty AlcoholsBioorganic & Medicinal Chemistry
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Silicateins - A Novel Paradigm in Bioinorganic Chemistry: Enzymatic Synthesis of Inorganic Polymeric Silica

2013

The inorganic matrix of the siliceous skeletal elements of sponges, that is, spicules, is formed of amorphous biosilica. Until a decade ago, it remained unclear how the hard biosilica monoliths of the spicules are formed in sponges that live in a silica-poor (<50 mu m) aquatic environment. The following two discoveries caused a paradigm shift and allowed an elucidation of the processes underlying spicule formation; first the discovery that in the spicules only one major protein, silicatein, exists and second, that this protein displays a bio-catalytical, enzymatic function. These findings caused a paradigm shift, since silicatein is the first enzyme that catalyzes the formation of an inorga…

SpiculeNew horizonsPolymersNanotechnology02 engineering and technologyCatalysisCalcium Carbonate03 medical and health sciencesSponge spiculeAnimals030304 developmental biology0303 health sciencesInorganic polymerChemistrySilicatesOrganic ChemistrySubstrate (chemistry)Bioinorganic chemistryGeneral ChemistryEnzymatic synthesisSilicon Dioxide021001 nanoscience & nanotechnologyCathepsinsPoriferaChemistry BioinorganicChemical engineeringBiocatalysisInorganic matrixSuberites0210 nano-technology
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Enantioselective Guest Effect on the Spin State of a Chiral Coordination Framework

2015

The diversity of spin crossover (SCO) complexes that, on the one hand, display variable temperature, abruptness and hysteresis of the spin transition, and on the other hand, are spin-sensitive to the various guest molecules, makes these materials unique for the detection of different organic and inorganic compounds. We have developed a homochiral SCO coordination polymer with a spin transition sensitive to the inclusion of the guest 2-butanol, and these solvates with (R)- and (S)-alcohols demonstrate different SCO behaviours depending on the chirality of the organic analyte. A stereoselective response to the guest inclusion is detected as a shift in the temperature of the transition both fr…

Spin statesChemistryStereochemistryCoordination polymerOrganic ChemistryEnantioselective synthesisSpin transitionGeneral ChemistryCatalysisCrystallographychemistry.chemical_compoundSpin crossoverDiamagnetismMoleculeChirality (chemistry)Chemistry - A European Journal
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Pyrrolomycins as antimicrobial agents. Microwave-assisted organic synthesis and insights into their antimicrobial mechanism of action

2019

Abstract New compounds able to counteract staphylococcal biofilm formation are needed. In this study we investigate the mechanism of action of pyrrolomycins, whose potential as antimicrobial agents has been demonstrated. We performed a new efficient and easy method to use microwave organic synthesis suitable for obtaining pyrrolomycins in good yields and in suitable amount for their in vitro in-depth investigation. We evaluate the inhibitory activity towards Sortase A (SrtA), a transpeptidase responsible for covalent anchoring in Gram-positive peptidoglycan of many surface proteins involved in adhesion and in biofilm formation. All compounds show a good inhibitory activity toward SrtA, havi…

Staphylococcus aureusClinical BiochemistryPharmaceutical ScienceMicrobial Sensitivity Testsmedicine.disease_causeSettore BIO/19 - Microbiologia Generale01 natural sciencesBiochemistrychemistry.chemical_compoundBacterial ProteinsDrug DiscoverymedicinePyrrolesEnzyme InhibitorsMicrowavesMolecular BiologyEnzyme Assays010405 organic chemistryChemistryOrganic ChemistryBiofilmN-Acetylmuramoyl-L-alanine AmidaseAntimicrobialAminoacyltransferasesAntimicrobial resistance Pyrrolomycins Sortase A Staphylococcus aureus In-silico docking studies MAOS Pharmacokinetics studies Murein hydrolase activitySettore CHIM/08 - Chimica Farmaceutica0104 chemical sciencesAnti-Bacterial AgentsMolecular Docking Simulation010404 medicinal & biomolecular chemistryCysteine EndopeptidasesBiochemistryMechanism of actionDocking (molecular)Staphylococcus aureusSettore CHIM/03 - Chimica Generale E InorganicaSortase ABiofilmsPseudomonas aeruginosaMolecular MedicineOrganic synthesisPeptidoglycanmedicine.symptom
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Bioactive polyketides and alkaloids from Penicillium citrinum , a fungal endophyte isolated from Ocimum tenuiflorum

2013

Chemical investigation of the endophytic fungus Penicillium citrinum cultured on white beans or on rice led to the isolation of two new alkaloids (1 and 2), along with fourteen known polyketides (6-12, 14-20) and four known alkaloids (3-5, and 13). The structures of the isolated compounds were determined by extensive analysis of the 1D, 2D NMR, and MS data, and by comparison with the literature. Compound 13, which had been previously obtained only by chemical synthesis, was isolated as a natural product for the first time, while compound 6 was firstly reported as a fungal metabolite. A re-isolation of sclerotinin A (14) revealed it to be a diastereoisomeric mixture (14a and 14b), whose ster…

Staphylococcus aureusLymphomaStereochemistryAntineoplastic Agentsmedicine.disease_causeChemical synthesisEndophyteInhibitory Concentration 50Micechemistry.chemical_compoundAlkaloidsCell Line TumorDrug DiscoveryEndophytesmedicineAnimalsPenicillium citrinumCytotoxicityPharmacologyBiological ProductsNatural productMolecular StructurebiologyPenicilliumGeneral Medicinebiology.organism_classificationOcimumAnti-Bacterial AgentsOcimumchemistryStaphylococcus aureusPolyketidesAntibacterial activityFitoterapia
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Hydroxypropylcellulose as a novel green reservoir for the synthesis, stabilization, and storage of silver nanoparticles

2015

Muhammad Ajaz Hussain,1 Abdullah Shah,1 Ibrahim Jantan,2 Muhammad Raza Shah,3 Muhammad Nawaz Tahir,4 Riaz Ahmad,5 Syed Nasir Abbas Bukhari2 1Department of Chemistry, University of Sargodha, Sargodha, Pakistan; 2Drug and Herbal Research Centre, Faculty of Pharmacy, Universiti Kebangsaan Malaysia, Jalan Raja Muda Abdul Aziz, Kuala Lumpur, Malaysia; 3International Center for Chemical and Biological Sciences, University of Karachi, Karachi, Pakistan; 4Institute of Inorganic and Analytical Chemistry, Johannes Guttenberg University, Duesbergweg, Mainz, Germany; 5Centre for Advanced Studies in Physics (CASP), GC University, Lahore, Pakistan Abstract: Polysaccharides are attracting the vigil eye of…

Staphylococcus aureusSilverMaterials scienceScanning electron microscopeDrug StorageBiophysicsMetal NanoparticlesPharmaceutical ScienceBioengineeringNanotechnologyNanoreactorMicroscopy Atomic Forcenanobiotechnologyantimicrobial assaySilver nanoparticlestorageBiomaterialsAnti-Infective AgentsMicroscopy Electron TransmissionX-Ray DiffractionInternational Journal of NanomedicinePhase (matter)Spectroscopy Fourier Transform InfraredDrug DiscoveryEscherichia coliStaphylococcus epidermidisThin filmCelluloseOriginal ResearchAqueous solutiongreen synthesisOrganic Chemistrytechnology industry and agricultureGreen Chemistry TechnologyGeneral MedicinestabilityTransmission electron microscopyPseudomonas aeruginosaMicroscopy Electron ScanningSunlightAspergillus nigernanoreactorAbsorption (chemistry)Bacillus subtilisNuclear chemistryInternational Journal of Nanomedicine
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Multi-epoch VLTI-PIONIER imaging of the supergiant V766 Cen

2017

Context. The star V766 Cen (=HR 5171A) was originally classified as a yellow hypergiant but lately found to more likely be a 27-36 M red supergiant (RSG). Recent observations indicated a close eclipsing companion in the contact or common-envelope phase. Aims. Here, we aim at imaging observations of V766 Cen to confirm the presence of the close companion. Methods. We used near-infrared H-band aperture synthesis imaging at three epochs in 2014, 2016, and 2017, employing the PIONIER instrument at the Very Large Telescope Interferometer (VLTI). Results. The visibility data indicate a mean Rosseland angular diameter of 4.1 ± 0.8 mas, corresponding to a radius of 1575 ± 400 R. The data show an ex…

Stars: imagingAperture synthesisBinaries: eclipsingFOS: Physical sciencesAstrophysics01 natural sciences010309 opticsCommon envelopeBinaries: closeAngular diameter0103 physical sciencesmassive [Stars]Red supergiantStars: massiveYellow hypergiant010303 astronomy & astrophysicsSolar and Stellar Astrophysics (astro-ph.SR)PhysicsVery Large Telescopeeclipsing [Binaries]Astronomy and AstrophysicsRadiusAstrophysics - Solar and Stellar AstrophysicsSupergiantsSpace and Planetary Scienceimaging [Stars]Techniques: interferometricinterferometric [Techniques]Supergiantclose [Binaries]Astronomy &amp; Astrophysics
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Synthesis of Pyrrolidin-2-ones and of Staurosporine Aglycon (K-252c) by Intermolecular Michael Reaction

1999

Indolo[2,3-a]pyrrolo[3,4-c]carbazoles were isolated from nature, e.g., from low plants, especially fungi, as structurally rare natural substances. Responsible for naming and also the most important representative of this type is staurosporine (1), isolated from Streptomyces staurosporeus, and its aglycon (2), also known as staurosporinone or K-252c. 3,4-Disubstituted pyrrolidin-2-ones, a group of compounds with many interesting biological properties are related to staurosporinone. The most important property is the inhibition of protein kinase C (PKC), so that this antiproliferative agent can interfere with the cell cycle. The synthetic strategy, developed by us, allows the synthesis of pyr…

StaurosporinoneStereochemistryOrganic ChemistryIntermolecular forceEnantioselective synthesisCombinatorial chemistrychemistry.chemical_compoundchemistryNitroLactammedicineMichael reactionStaurosporineProtein kinase Cmedicine.drugThe Journal of Organic Chemistry
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