Search results for "taxanes"

showing 10 items of 23 documents

Synthesis of [5]Rotaxanes Containing Bi- and Tridentate Coordination Sites in the Axis

2010

A new example of a linear [5]rotaxane has been synthesized by using the traditional "gathering-and-threading" approach but based on an unusual axle incorporating a symmetrical bis(bidentate) chelating fragment built on a 4,7-phenanthroline core. The stoppering reaction is particularly noteworthy since, instead of using a trivial bulky stopper as precursor to the blocking group, two semistoppered copper-complexed [2]pseudorotaxanes (namely [2]semirotaxanes) are used, which leads to the desired [5]rotaxane in good yield. The efficiency of the method relies on the use of "click" chemistry, with its very mild conditions, and on the protection by a transition-metal (copper(I)) of the various coo…

chemistry.chemical_classificationRotaxaneDenticityLigandStereochemistryclick chemistry; copper; lithium; rotaxanes; zincOrganic Chemistrychemistry.chemical_elementGeneral ChemistryZincCatalysischemistry.chemical_compoundCrystallographychemistryClick chemistryChelationTerpyridineCounterionChemistry - A European Journal
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Photocontrolled On-Surface Pseudorotaxane Formation with Well-Ordered Macrocycle Multilayers.

2016

The photoinduced pseudorotaxane formation between a photoresponsive axle and a tetralactam macrocycle was investigated in solution and on glass surfaces with immobilized multilayers of macrocycles. In the course of this reaction, a novel photoswitchable binding station with azobenzene as the photoswitchable unit and diketopiperazine as the binding station was synthesized and studied by NMR and UV/Vis spectroscopy. Glass surfaces have been functionalized with pyridine-terminated SAMs and subsequently with multilayers of macrocycles through layer-by-layer self assembly. A preferred orientation of the macrocycles could be confirmed by NEXAFS spectroscopy. The photocontrolled deposition of the …

Supramolecular chemistryTetralactam macrocyclesurface chemistry02 engineering and technology010402 general chemistryLinear dichroismPhotochemistry01 natural sciencessupramolecular chemistryCatalysischemistry.chemical_compoundSpectroscopyta116pseudorotaxanesphotochemistryOrganic ChemistryGeneral Chemistry021001 nanoscience & nanotechnologyXANES0104 chemical sciencesazobenzeneAzobenzenechemistryNexafs spectroscopySelf-assembly0210 nano-technologyChemistry (Weinheim an der Bergstrasse, Germany)
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A modular "toolbox" approach to flexible branched multimacrocyclic hosts as precursors for multiply interlocked architectures.

2008

Tetralactam macrocycles can be functionalized by a variety of cross-coupling reactions. A modular “toolbox” strategy is presented that allows 1) several tetralactam macrocycles to be covalently connected with each other or with a central spacer, 2) the macrocycles to be substituted with or connected to different chromophores, and 3) metal-coordination sites to be attached to the macrocycles. With this approach a series of different oligo-macrocyclic hosts was obtained with great structural diversity and enormous potential for further functionalization. Rotaxanes made on the basis of these macrocycles have been synthesized to demonstrate their utility in building more complex supramolecular …

Macrocyclic CompoundsLactamsMolecular StructureRotaxanesbusiness.industryChemistryOrganic ChemistryCatenaneSupramolecular chemistryMolecular ConformationStructural diversityNanotechnologyGeneral ChemistryModular designCrystallography X-RayCombinatorial chemistryCatalysisToolboxCyclizationLuminescent MeasurementsSpectroscopy Fourier Transform InfraredbusinessChemistry (Weinheim an der Bergstrasse, Germany)
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Photoinduced Electron Transfer in Multiporphyrinic Interlocked Structures: The Effect of Copper(I) Coordination in the Central Site

2004

Photoinduced processes have been determined in a [2]catenane containing a zinc(II) porphyrin, a gold(III) porphyrin, and two free phenanthroline binding sites, Zn-Au(+), and in the corresponding copper(I) phenanthroline complex, Zn-Cu(+)-Au(+). In acetonitrile solution Zn-Au(+) is present in two different conformations: an extended one, L, which accounts for 40 % of the total, and a compact one, S. In the L conformation, the electron transfer from the excited state of the Zn porphyrin to the gold-porphyrin unit (k = 1.3x10(9) s(-1)) is followed by a slow recombination (k = 8.3x10(7) s(-1)) to the ground state. The processes in the S conformation cannot be clearly resolved but a charge-separ…

RotaxanesMetalloporphyrinsPhotochemistryPhenanthrolineCatenaneMolecular Conformationchemistry.chemical_elementElectronsPhotochemistryCatalysisPhotoinduced electron transferElectron Transportchemistry.chemical_compoundElectron transferChemistryOrganic ChemistryGeneral ChemistryPorphyrinCopperZincCrystallographyEnergy TransferSpectrophotometryExcited stateGoldGround stateCopperChemistry - A European Journal
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Selectivity of cyclodextrins as a parameter to tune the formation of pseudorotaxanes and micelles supramolecular assemblies. A systematic SANS study

2011

Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG geförderten) Allianz- bzw. Nationallizenz frei zugänglich. This publication is with permission of the rights owner freely accessible due to an Alliance licence and a national licence (funded by the DFG, German Research Foundation) respectively. We studied the formation of polypseudorotaxanes formed with cyclodextrins (CDs) threading a copolymer chain that forms self-assembled structures in water. The size of the CD cavity was chosen such that it is block selective with respect to the formation of inclusion complexes and therefore in terms of altering the structure of the copolymer self-assemblies in a systematic fashio…

Neutron scattering supramolecular chemistry cyclodextrin pseudorotaxaneschemistry.chemical_classificationMaterials scienceCyclodextrinSupramolecular chemistry02 engineering and technologyGeneral ChemistryNeutron scattering010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesSmall-angle neutron scatteringMicelle0104 chemical sciencesCrystallographychemistryCopolymerddc:5300210 nano-technologySelectivityDissolutionSettore CHIM/02 - Chimica Fisica
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Cyclic [2]Pseudorotaxane Tetramers Consisting of Two Rigid Rods Threaded through Two Bis-Macrocycles: Copper(I)-Templated Synthesis and X-ray Structu…

2008

Variously substituted coordinating rigid rods have been synthesized which incorporate a central 4,7-phenanthroline nucleus attached to two 2-pyridyl groups via its 3 and 8 positions, so as to yield bis-bidentate chelates, the two-coordinating axes of the chelates being parallel to one another. Regardless of the nature of the substituents borne by the rods, the copper(I)-induced threading reaction of two such rods through the rings of two bis-macrocycles affords in a quantitative yield the 4-copper(I) threaded assembly. The [2]pseudorotaxane tetramers thus obtained have been fully characterized in solution and, for one of them, an X-ray structure could be obtained, confirming the threaded na…

Models MolecularMacrocyclic CompoundsMolecular StructureRotaxanesChemistryX-raychemistry.chemical_elementStereoisomerismStereoisomerismGeneral ChemistryCrystallography X-RayBiochemistryCopperCatalysisRodCrystallographyColloid and Surface ChemistryYield (chemistry)Organometallic CompoundsThreading (manufacturing)MoleculeCopperPhenanthrolinesGroup 2 organometallic chemistryJournal of the American Chemical Society
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Relationship between Thymidylate synthase and p53 and response versus taxane adjuvant chemotherapy for breast carcinoma

2011

Many drugs can be used for adjuvant therapy of breast cancer, including anthracyclines, cyclophosphamide, 5-fluorouracil (5-fU) and, recently, taxanes (TXT) have shown promising results. 5-FU blocks thymidylate synthase (TS) which cross-links p53 mRNA, inhibiting its synthesis. TS overexpression is one of the main mechanisms involved in 5-FU drug resistance. Enough p53 mutations can confer resistance to chemotherapy using anthracyclines and 5-FU, while are associated with improved responses to TXT. The aim of this study was to examine the TS and p53 levels in tumor samples and to compare the efficacy of FEC (5-FU, epirubicin, cyclophosphamide) and TXT chemotherapy in a group of patients wit…

Settore BIO/14 - Farmacologiathymidylate synthase p53 breast cancer fluorouracil taxanesSettore MED/08 - Anatomia Patologica
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Ion-Pairing Effects in the Self-Assembly of a Fluorescent Pseudorotaxane

2006

Herein we report on the self-assembly, in a low polarity solvent, of a pseudorotaxane species comprising binaphthyl-26-crown-8 (BN26C8) as the macrocyclic host and anthracenyl-benzylammonium as the threadlike positively charged guest (ABH+). Absorption and luminescence data reveal a very efficient energy transfer process occurring from the binaphthyl to the anthracene singlet excited states. The self-assembly is highly dependent on the nature of the counteranion confirming the crucial role played by it in the competition between the self-assembly process and the formation of ion pairs (ABH+X-). This behavior can be readily evidenced in dilute solutions from the analysis of the luminescence …

AnthraceneIon pairsRotaxanesPhotochemistryStereochemistryOrganic ChemistrySupramolecular chemistrySelf-assemblychemistry.chemical_compoundCrystallographyTRISPHATMolecular recognitionchemistryHexafluorophosphateddc:540Proton NMRSinglet stateMolecular recognitionPhysical and Theoretical ChemistryLuminescenceEuropean Journal of Organic Chemistry
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Autonomous artificial nanomotor powered by sunlight

2006

Light excitation powers the reversible shuttling movement of the ring component of a rotaxane between two stations located at a 1.3-nm distance on its dumbbell-shaped component. The photoinduced shuttling movement, which occurs in solution, is based on a “four-stroke” synchronized sequence of electronic and nuclear processes. At room temperature the deactivation time of the high-energy charge-transfer state obtained by light excitation is ≈10 μs, and the time period required for the ring-displacement process is on the order of 100 μs. The rotaxane behaves as an autonomous linear motor and operates with a quantum efficiency up to ≈12%. The investigated system is a unique example of an artif…

Models MolecularLuminescenceMagnetic Resonance SpectroscopyTime FactorsRotaxaneLightRotaxanesUltraviolet RaysPhotochemistryMovementMolecular ConformationElectronsPhotochemistryAbsorptionQUIMICA ORGANICAPhenothiazinesRotaxaneElectrochemistryNanotechnologyNanomotorAbsorption (electromagnetic radiation)Molecular machinePhotolysisMultidisciplinaryChemistrybusiness.industryMolecular Motor ProteinsPhotodissociationTemperatureLinear motorKineticsNanoscienceFluid solutionSpectrophotometryPhysical SciencesSunlightOptoelectronicsQuantum efficiencyElectronicsLuminescencebusinessSupramolecular chemistry
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An overview on anti-tubulin agents for the treatment of lymphoma patients

2020

Anti-tubulin agents constitute a large class of compounds with broad activity both in solid tumors and hematologic malignancies, due to the interference with microtubule dynamics. Since microtubules play crucial roles in the regulation of the mitotic spindles, the interference with their function usually leads to a block in cell division with arrest at the metaphase/anaphase junction of mitosis, followed to apoptosis. This explains the reason why tubulin-binding agents (TBAs) proved to be extremely active in patients with cancer. Several anti-tubulin agents are indicated in the treatment of patients with lymphomas both alone and in combination chemotherapy regimens. The article reviews the …

0301 basic medicineVinca alkaloidsLymphomaMitosisAntineoplastic AgentsApoptosismacromolecular substancesMicrotubulesAntibody drug conjugatesTaxanes03 medical and health sciences0302 clinical medicineTubulinMicrotubulemedicineAnimalsHumansMaytansinePharmacology (medical)MetaphaseMitosisAnaphasePharmacologybiologybusiness.industryCancerCombination chemotherapymedicine.diseaseTubulin ModulatorsLymphoma030104 developmental biologyTubulinEpothilones030220 oncology & carcinogenesisbiology.proteinCancer researchDolastatinsbusinessPharmacology & Therapeutics
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