Synthetic approaches for the conjugation of porphyrins and related macrocycles to peptides and proteins.
about
Unique diagnostic and therapeutic roles of porphyrins and phthalocyanines in photodynamic therapy, imaging and theranosticsThe PDT activity of free and pegylated pheophorbide a against an amelanotic melanoma transplanted in C57/BL6 mice.Receptor selective ruthenium-somatostatin photosensitizer for cancer targeted photodynamic applications.Syntheses and cellular investigations of di-aspartate and aspartate-lysine chlorin e(6) conjugates.Mechanisms of growth inhibition of primary prostate epithelial cells following gamma irradiation or photodynamic therapy include senescence, necrosis, and autophagy, but not apoptosisBioconjugatable, PEGylated Hydroporphyrins for Photochemistry and Photomedicine. Narrow-Band, Red-Emitting Chlorins.Efficient access to β-vinylporphyrin derivatives via palladium cross coupling of β-bromoporphyrins with N-tosylhydrazones.Biological detection by optical oxygen sensing.Synthesis and biological evaluation of peptide-conjugated phthalocyanine photosensitizers with highly hydrophilic modifications.Synthesis and in vitro photodynamic activities of an integrin-targeting cRGD-conjugated zinc(II) phthalocyanine.Porphyrin-based cationic amphiphilic photosensitisers as potential anticancer, antimicrobial and immunosuppressive agentsFlexible synthesis of cationic peptide-porphyrin derivatives for light-triggered drug delivery and photodynamic therapy.A phthalocyanine-peptide conjugate with high in vitro photodynamic activity and enhanced in vivo tumor-retention property.Endolysosomal targeting of a clinical chlorin photosensitiser for light-triggered delivery of nano-sized medicines.Tetraphenylporphyrin as a protein label for triple detection analytical systems.Hydrophilic tetracarboxy bacteriochlorins for photonics applications.Huisgen-based conjugation of water-soluble porphyrins to deprotected sugars: towards mild strategies for the labelling of glycans.Anticancer nanoparticulate polymer-drug conjugate.Hydrophilic bioconjugatable trans-AB-porphyrins and peptide conjugatesNear-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 systemSynthesis and Development of Lipoprotein-Based Nanocarriers for Light-Activated Theranostics
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P2860
Synthetic approaches for the conjugation of porphyrins and related macrocycles to peptides and proteins.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on April 2011
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Synthetic approaches for the c ...... cles to peptides and proteins.
@en
Synthetic approaches for the c ...... cles to peptides and proteins.
@nl
type
label
Synthetic approaches for the c ...... cles to peptides and proteins.
@en
Synthetic approaches for the c ...... cles to peptides and proteins.
@nl
prefLabel
Synthetic approaches for the c ...... cles to peptides and proteins.
@en
Synthetic approaches for the c ...... cles to peptides and proteins.
@nl
P2860
P356
P1476
Synthetic approaches for the c ...... cles to peptides and proteins.
@en
P2093
Cristina M A Alonso
Ross W Boyle
P2860
P304
P356
10.1039/C0PP00366B
P577
2011-04-01T00:00:00Z