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High content screening as high quality assay for biological evaluation of photosensitizers in vitroImpact of substituents and nonplanarity on nickel and copper porphyrin electrochemistry: first observation of a Cu(II)/Cu(III) reaction in nonaqueous media.Synthesis and biological evaluation of a library of glycoporphyrin compounds.Transferrin conjugation does not increase the efficiency of liposomal Foscan during in vitro photodynamic therapy of oesophageal cancer.Lead Structures for Applications in Photodynamic Therapy. 6. Temoporfin Anti-Inflammatory Conjugates to Target the Tumor Microenvironment for In Vitro PDT.Specific Drug Formulation Additives: Revealing the Impact of Architecture and Block Length Ratio.The characterization of an intestine-like genomic signature maintained during Barrett's-associated adenocarcinogenesis reveals an NR5A2-mediated promotion of cancer cell survival.Temoporfin (Foscan®, 5,10,15,20-tetra(m-hydroxyphenyl)chlorin)--a second-generation photosensitizer.mTHPC--a drug on its way from second to third generation photosensitizer?The translocator protein as a potential molecular target for improved treatment efficacy in photodynamic therapy.Crystal structure of 5-tert-but-yl-10,15,20-tri-phenyl-porphyrin.Drug Discovery Approaches Utilizing Three-Dimensional Cell Culture.Effects of preparation conditions of poly(lactide-co-glycolide) nanoparticles loaded with amphiphilic porphyrins and their photoactivities.A two-pronged attack on DNA: targeting guanine quadruplexes with nonplanar porphyrins and DNA-binding small molecules.Lead structures for applications in photodynamic therapy. 5. Synthesis and biological evaluation of water soluble phosphorus(V) 5,10,15,20-tetraalkylporphyrins for PDT.Pdots, a new type of nanoparticle, bind to mTHPC via their lipid modified surface and exhibit very high FRET efficiency between the core and the sensitizer.Synthesis and biological evaluation of Foscan® bile acid conjugates to target esophageal cancer cells.Simple but powerful: phenanthroline-based small molecules for cellular imaging and cancer screening.Contribution of bacteriochlorophyll conformation to the distribution of site-energies in the FMO protein.(5,15-Dianthracen-9-yl-10,20-dihexyl-porphyrinato)nickel(II): a planar nickel(II) porphyrin.Structural investigation of 5,10-A2B2-type porphyrins: palladium(II) and zinc(II) complexes of 5,10-dibromo-15,20-bis(4-methylphenyl)porphyrin.Comparative Analysis of the Conformations of Symmetrically and Asymmetrically Deca- and Undecasubstituted Porphyrins Bearing Meso-Alkyl or -Aryl Groups.Oxasmaragdyrin-ferrocene and oxacorrole-ferrocene conjugates: synthesis, structure, and nonlinear optical properties.Self-assembled rows of Ni porphyrin dimers on the Ag(111) surface.The dithianyl group as a synthon in porphyrin chemistry: condensation reactions and preparation of formylporphyrins under basic conditions.Computational quantification of the physicochemical effects of heme distortion: redox control in the reaction center cytochrome subunit of Blastochloris viridis.Aggregation of 2,3-dihydroxy-etiochlorin I. An amphiphilic model compound for photodynamic therapy and green heme d.Synthesis, transformations, and comparative studies of porphyryl acrylic acids and their homologues.Metal-Catalyzed Oxidative Cyclizations of a,c-Biladiene Salts Bearing 1- and/or 19-Arylmethyl Substituents: Macrocyclic Products and Their Chemistry.Generation of Triplet Excited States via Photoinduced Electron Transfer in meso-anthra-BODIPY: Fluorogenic Response toward Singlet Oxygen in Solution and in Vitro.Hydrogen-bonding patterns in six derivatives of 2,4-dimethylpyrrole.Nucleophilic substitution as a tool for the synthesis of unsymmetrical porphyrins.Influence of the core conformation on the NH-tautomerism in porphyrins: a study of meso-(1,3-dithian-2-yl)porphyrins.How green is green chemistry? Chlorophylls as a bioresource from biorefineries and their commercial potential in medicine and photovoltaics.On the correlation between hydrophobicity, liposome binding and cellular uptake of porphyrin sensitizers.Enhancing the photoluminescence of surface anchored metal-organic frameworks: mixed linkers and efficient acceptors.Water-soluble, neutral 3,5-diformyl-BODIPY with extended fluorescence lifetime in a self-healable chitosan hydrogel.Delayed release singlet oxygen sensitizers based on pyridone-appended porphyrins.Cubane Cross-Coupling and Cubane-Porphyrin Arrays.The Janus-faced chromophore: a donor-acceptor dyad with dual performance in photon up-conversion.
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Mathias O Senge
@ast
Mathias O Senge
@en
Mathias O Senge
@es
Mathias O Senge
@nl
Mathias O Senge
@sl
type
label
Mathias O Senge
@ast
Mathias O Senge
@en
Mathias O Senge
@es
Mathias O Senge
@nl
Mathias O Senge
@sl
altLabel
Mathias O. Senge
@en
prefLabel
Mathias O Senge
@ast
Mathias O Senge
@en
Mathias O Senge
@es
Mathias O Senge
@nl
Mathias O Senge
@sl
P1053
F-1504-2011
P106
P21
P31
P3829
P496
0000-0002-7467-1654