Search results for "Small Molecule"

showing 10 items of 197 documents

The Synthesis, Condensation, and Luminescence of Stilbenoid Oligomers with Alkoxysilane End Groups

2001

ABSTRACTA synthetic route to highly luminescent organic semiconductors with curable alkoxysilyl groups is described. Monodisperse oligo(phenylenevinylene)s are rigidly connected to di- and triethoxysilanes via Heck reactions or via cross-metathesis. Hydrolysis of the silicic esters yields silanols condensing to linear and cyclic oligo-OPV-siloxanes or to three-dimensional networks, thus allowing the transformation of small molecules to fluorescent materials with well-defined chromophores. Transparent films are obtained by casting of soluble cyclosiloxanes and from OPV-silanetriols, the latter can be cured to insoluble networks.

Organic semiconductorHydrolysisChemistryDispersityCondensationPolymer chemistryChromophoreLuminescencePhotochemistryCastingSmall moleculeMRS Proceedings
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Does Ligand Symmetry Play a Role in the Stabilization of DNA G-Quadruplex Host-Guest Complexes?

2014

In efforts to find agents with improved biological activity against cancer cells, recent years have seen an increased interest in the study of small molecules able to bind the deoxyribonucleic acid (DNA) when it assumes secondary structures known as G-quadruplexes (G4s) preferring them over the B form. Currently, several compounds reported in literature have already shown to be good candidates as G4s DNA stabilizers. Even though some specific features for the G4s affinity are known, such as a π-delocalized system able to stack at the top/end of a G-tetrad and positively charged substituents able to interact with the grooves, it is not clear yet what kind of structural features affect more t…

PharmacologyGene isoformLigandStereochemistryOrganic ChemistryAntineoplastic AgentsDNATelomereLigandsG-quadruplexSettore CHIM/08 - Chimica FarmaceuticaBiochemistrySmall moleculeG-Quadruplexeschemistry.chemical_compoundOrder (biology)chemistrySettore CHIM/03 - Chimica Generale E InorganicaAnticancer drugs DNA G-quadruplex host-guest complexes ligand symmetry point group symmetryDrug DiscoveryMolecular symmetryHumansMolecular MedicineDNAStabilizer (chemistry)Current Medicinal Chemistry
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Multi or Single-Kinase Inhibitors to Counteract Drug Resistance in Cancer: What is New?

2023

The concept of protein kinase inhibition starts from the groundbreaking research on the role of these proteins in the regulation of fundamental processes, including proliferation, cell cycle, apoptosis, metabolism, and inflammation. Kinase genetic mutations, as well as overexpression and dysregulation, can contribute to the development of several diseases, including neoplasms, leading to relapses and resistance to standard drug chemotherapy [1-3].

PharmacologySmall molecules kinase inhibitorspolypharmacologycovalent kinase inhibitorsallosteric inhibitorsDrug DiscoveryOrganic ChemistryMolecular Medicineanticancer drug combinationsBiochemistrykinase genetic aberrationSettore CHIM/08 - Chimica Farmaceutica
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Fragment- and negative image-based screening of phosphodiesterase 10A inhibitors.

2019

A novel virtual screening methodology called fragment- and negative image-based (F-NiB) screening is introduced and tested experimentally using phosphodiesterase 10A (PDE10A) as a case study. Potent PDE10A-specific small-molecule inhibitors are actively sought after for their antipsychotic and neuroprotective effects. The F-NiB combines features from both fragment-based drug discovery and negative image-based (NIB) screening methodologies to facilitate rational drug discovery. The selected structural parts of protein-bound ligand(s) are seamlessly combined with the negative image of the target's ligand-binding cavity. This cavity- and fragment-based hybrid model, namely its shape and electr…

PharmacologyVirtual screening010405 organic chemistryDrug discoveryChemistryPhosphodiesterase InhibitorsPhosphoric Diester HydrolasesOrganic ChemistryFragment-based lead discoveryAb initioDrug Evaluation PreclinicalPhosphodiesteraseComputational biology01 natural sciencesBiochemistrySmall molecule0104 chemical sciencesMolecular Docking Simulation010404 medicinal & biomolecular chemistryDocking (molecular)Drug DiscoveryMolecular MedicineHumansPharmacophoreChemical biologydrug designREFERENCES
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Selective Modulation of Aβ42 Production in Alzheimers Disease: Non-Steroidal Anti-Inflammatory Drugs and Beyond

2006

The amyloid-β (Aβ) peptides and in particular the longer, highly amyloidogenic isoform Aβ42 are believed by many to be the central disease-causing agents in Alzheimers disease (AD). Consequently, academic and pharmaceutical laboratories have focused on elucidating the mechanisms of Aβ production and developing strategies to diminish Aβ formation for treatment or prevention of AD. The most substantial advances have been made with respect to inhibitors of the γ-secretase enzyme, which catalyzes the final step in the generation of Aβ from the amyloid precursor protein (APP). Highly potent γ-secretase inhibitors which suppress production of all Aβ peptides are available today. However, due to t…

Pharmacologychemistry.chemical_classificationGene isoformbiologybusiness.industryNotch signaling pathwayPharmacologymedicine.diseaseSmall moleculePathogenesisEnzymechemistryMechanism of actionDrug DiscoveryImmunologymedicineAmyloid precursor proteinbiology.proteinAlzheimer's diseasemedicine.symptombusinessCurrent Pharmaceutical Design
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Tetradihydrobenzoquinonate and Tetrachloranilate Zr(IV) Complexes: Single-Crystal-to-Single-Crystal Phase Transition and Open-Framework Behavior for …

2013

The molecular complexes K4[Zr(DBQ)4] and K 4[Zr(CA)4], where DBQ2- and CA2- stand respectively for deprotonated dihydroxybenzoquinone and chloranilic acid, are reported. The anionic metal complexes consist of Zr(IV) surrounded by four O,O-chelating ligands. Besides the preparation and crystal structures for the two complexes, we show that in the solid state the DBQ complex forms a 3-D open framework (with 22% accessible volume) that undergoes a crystal-to-crystal phase transition to a compact structure upon guest molecule release. This process is reversible. In the presence of H2O, CO2, and other small molecules, the framework opens and accommodates guest molecules. CO2 adsorption isotherms…

Phase transition010405 organic chemistryChemistryCrystal structure[CHIM.MATE]Chemical Sciences/Material chemistryCrystal structure010402 general chemistry01 natural sciencesSmall molecule3. Good health0104 chemical sciencesMolecular complexesInorganic ChemistryMetalCrystallographychemistry.chemical_compoundDeprotonationChloranilic acidvisual_art[ CHIM.MATE ] Chemical Sciences/Material chemistryvisual_art.visual_art_mediumMoleculePhysical and Theoretical ChemistrySingle crystalMolecular science
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Optimization of anti-proliferative activity using a screening approach with a series of bis-heterocyclic G-quadruplex ligands

2013

Abstract Using a phenotypic screening and SAR optimization approach, a phenyl-bis-oxazole derivative has been identified with anti-proliferative activity, optimized with the use of a panel of cancer cell lines. The lead compound was synthesized by means of a short and effective two-step synthesis using Pd-catalyzed direct arylation. The compound stabilizes several quadruplex DNA sequences including a human telomeric DNA and one from the promoter of the HSP90 gene, although the structure–activity relationships of the series are not obviously related to the quadruplex binding.

Phenotypic screeningClinical BiochemistryPharmaceutical ScienceG-quadruplexLigandsBiochemistrychemistry.chemical_compoundInhibitory Concentration 50Structure-Activity RelationshipHeterocyclic CompoundsCell Line TumorDrug DiscoveryHumansMolecular BiologyGeneCell ProliferationOrganic ChemistryCombinatorial chemistrySmall moleculeSettore CHIM/08 - Chimica FarmaceuticaG-QuadruplexeschemistryMolecular MedicineHuman genomeQuadruplex Anti-proliferative Phenotypic screening Telomerase OxazolesDrug Screening Assays AntitumorLead compoundDerivative (chemistry)DNA
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Convergence of Nuclear Magnetic Shieldings in the Kohn-Sham Limit for Several Small Molecules.

2015

Convergence patterns and limiting values of isotropic nuclear magnetic shieldings were studied for several small molecules (N2, CO, CO2, NH3, CH4, C2H2, C2H4, C2H6, and C6H6) in the Kohn-Sham limit. Individual results of calculations using dedicated families of Jensen's basis sets (pcS-n and pcJ-n) were fitted toward the complete basis set limit (CBS) using a simple two-parameter formula. Several density functionals were used; calculated vibrational corrections (ZPV) applied; and, for comparison purposes, similar calculations performed using RHF, MP2, SOPPA, SOPPA(CCSD), and CCSD(T) methods and additionally, the aug-cc-pVTZ-J basis set. Finally, the CBS estimated results were critically com…

PhysicsBasis (linear algebra)AtomIsotropyConvergence (routing)Kohn–Sham equationsLimit (mathematics)Physical and Theoretical ChemistryAtomic physicsSmall moleculeBasis setComputer Science ApplicationsJournal of chemical theory and computation
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Photoelectron spectra from first principles: from the many-body to the single-particle picture

2008

We derive a many-body method to evaluate photoelectron spectra of atoms, molecules and clusters from first principles. The excitation energies and the spectroscopic factors are calculated from the linear-response time-dependent density functional theory. The method is applied to noble metal anions, anionic clusters and to neutral small molecules. Our approach shows significant improvement over a simple single-particle treatment and gives an insight into the necessary conditions under which the single-particle picture holds. The consideration of the spectroscopic factor is shown to be crucial for the correct description of inner valence photoelectron peaks.

PhysicsValence (chemistry)General Physics and Astronomyengineering.materialSmall moleculeMany bodySpectral linePhysics::Atomic and Molecular ClustersengineeringMoleculeDensity functional theoryNoble metalAtomic physicsExcitationNew Journal of Physics
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Click modification of multifunctional liposomes bearing hyperbranched polyether chains.

2014

Aiming at controlled modification of liposomal surface structures, we describe a postpreparational approach for surface derivatization of a new type of multifunctional, sterically stabilized liposomes. Application of dual centrifugation (DC) resulted in high encapsulation efficiencies above 50% at very small batch sizes with a total volume of 150 μL, which were conductive to fast and efficient optimization of variegated surface modification reactions. Cholesterol-polymer amphiphiles, including complex hyperbranched polyether structures bearing 1-4 terminal alkynes, were used in DC formulations to provide steric stabilization. The alkyne moieties were explored as anchors for the conjugation …

Polymers and PlasticsPolymersAlkyneBioengineeringCell LinePolyethylene GlycolsBiomaterialsPolymer chemistryAmphiphileMaterials ChemistryFluorescence Resonance Energy TransferMoleculeAnimalschemistry.chemical_classificationLiposomeMicroscopy ConfocalBrainEndothelial CellsSmall moleculeCombinatorial chemistryRatsFörster resonance energy transferchemistryDoxorubicinAlkynesLiposomesClick chemistrySurface modificationClick ChemistryBiomacromolecules
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