Porphyrin, chlorin, and bacteriochlorin isothiocyanates: useful reagents for the synthesis of photoactive bioconjugates.
about
Unique diagnostic and therapeutic roles of porphyrins and phthalocyanines in photodynamic therapy, imaging and theranosticsBioconjugatable porphyrins bearing a compact swallowtail motif for water solubility.Development and characterization of novel photosensitizer : scFv conjugates for use in photodynamic therapy of cancer.Identification of methicillin-resistant Staphylococcus aureus-specific peptides for targeted photoantimicrobial chemotherapy.Synthesis of BODIPY-Peptide Conjugates for Fluorescence Labeling of EGFR Overexpressing Cells.Synthesis and biological investigations of a ZnPc-antiCEA bioconjugate for imaging of colorectal cancerA chemically modified antibody mediates complete eradication of tumours by selective disruption of tumour blood vessels.Porphyrin conjugated with serum albumins and monoclonal antibodies boosts efficiency in targeted destruction of human bladder cancer cells.High-level production of porphyrins in metabolically engineered Escherichia coli: systematic extension of a pathway assembled from overexpressed genes involved in heme biosynthesis.meso-arylporpholactones and their reduction productsMechanisms of growth inhibition of primary prostate epithelial cells following gamma irradiation or photodynamic therapy include senescence, necrosis, and autophagy, but not apoptosisDesign and synthesis of water-soluble bioconjugatable trans-AB-porphyrinsActivatable organic near-infrared fluorescent probes based on a bacteriochlorin platform: synthesis and multicolor in vivo imaging with a single excitation.Photosensitiser-antibody conjugates for photodynamic therapy.Synthetic approaches for the conjugation of porphyrins and related macrocycles to peptides and proteins.Antibodies armed with photosensitizers: from chemical synthesis to photobiological applications.Modifications of Porphyrins and Hydroporphyrins for Their Solubilization in Aqueous Media.Mono- and tri-cationic porphyrin-monoclonal antibody conjugates: photodynamic activity and mechanism of action.Isothiocyanato boron dipyrromethenes--the first BODIPY analogues of fluorescein isothiocyanate.Shiga-like toxin subunit B (SLTB)-enhanced delivery of chlorin e6 (Ce6) improves cell killing.The development and characterisation of porphyrin isothiocyanate-monoclonal antibody conjugates for photoimmunotherapy.Sparsely substituted chlorins as core constructs in chlorophyll analogue chemistry. I. Synthesis.Hydrophilic tetracarboxy bacteriochlorins for photonics applications.Synthesis and Spectral Properties of meso-Arylbacteriochlorins, Including Insights into Essential Motifs of their Hydrodipyrrin Precursors.Amphiphilic, hydrophilic, or hydrophobic synthetic bacteriochlorins in biohybrid light-harvesting architectures: consideration of molecular designs.Cellular uptake of octaarginine-conjugated tetraarylporphyrin included by per-O-methylated β-cyclodextrin.A novel fluoro-chromogenic click reaction for the labelling of proteins and nanoparticles with near-IR theranostic agents.Chlorophyll-Inspired Red-Region Fluorophores: Building Block Synthesis and Studies in Aqueous Media.β-Alkyloxazolochlorins: Revisiting the Ozonation of Octaalkylporphyrins, and Beyond.A convenient method for multicolour labelling of proteins with BODIPY fluorophores via tyrosine residues.Production of uroporphyrinogen III, which is the common precursor of all tetrapyrrole cofactors, from 5-aminolevulinic acid by Escherichia coli expressing thermostable enzymes.Bovine serum albumin coated nanoparticles for in vitro activated fluorescence.Palette of lipophilic bioconjugatable bacteriochlorins for construction of biohybrid light-harvesting architecturesSynthetic bacteriochlorins with integral spiro-piperidine motifsElaboration of an unexplored substitution site in synthetic bacteriochlorinsDe novo synthesis and photophysical characterization of annulated bacteriochlorins. Mimicking and extending the properties of bacteriochlorophyllsNear-infrared tunable bacteriochlorins equipped for bioorthogonal labelingPolarity-tunable and wavelength-tunable bacteriochlorins bearing a single carboxylic acid or NHS ester. Use in a protein bioconjugation model system
P2860
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P2860
Porphyrin, chlorin, and bacteriochlorin isothiocyanates: useful reagents for the synthesis of photoactive bioconjugates.
description
2002 nî lūn-bûn
@nan
2002 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի մարտին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Porphyrin, chlorin, and bacter ...... of photoactive bioconjugates.
@ast
Porphyrin, chlorin, and bacter ...... of photoactive bioconjugates.
@en
type
label
Porphyrin, chlorin, and bacter ...... of photoactive bioconjugates.
@ast
Porphyrin, chlorin, and bacter ...... of photoactive bioconjugates.
@en
prefLabel
Porphyrin, chlorin, and bacter ...... of photoactive bioconjugates.
@ast
Porphyrin, chlorin, and bacter ...... of photoactive bioconjugates.
@en
P2093
P356
P1476
Porphyrin, chlorin, and bacter ...... of photoactive bioconjugates.
@en
P2093
P304
P356
10.1021/BC015547X
P577
2002-03-01T00:00:00Z