184 results on '"Eggleston, Ian M."'
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2. Tripodal BODIPY‐Tagged and Functional Molecular Probes: Synthesis, Computational Investigations and Explorations by Multiphoton Fluorescence Lifetime Imaging Microscopy.
3. Biofilm-specific uptake of a 4-pyridone-based iron chelator by Pseudomonas aeruginosa
4. An intestinal paracellular pathway biased toward positively-charged macromolecules
5. Peptide-Targeted Photosensitisers: Synthesis and Applications in Photobiology
6. Mechanistic studies of a cell-permeant peptide designed to enhance myosin light chain phosphorylation in polarized intestinal epithelia
7. Chemical approaches for the enhancement of 5-aminolevulinic acid-based photodynamic therapy and photodiagnosis
8. Enhanced paracellular transport of insulin can be achieved via transient induction of myosin light chain phosphorylation
9. (Digital Presentation) Peptide Targeting of Photosensitisers for Photodynamic Therapy and Drug Delivery Applications
10. Daylight-PDT: everything under the sun
11. Photochemical internalisation of a macromolecular protein toxin using a cell penetrating peptide-photosensitiser conjugate
12. Codelivery of a cytotoxin and photosensitiser via a liposomal nanocarrier: a novel strategy for light-triggered cytosolic release† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c8nr04048f
13. Effective photoinactivation of Gram-positive and Gram-negative bacterial strains using an HIV-1 Tat peptide—porphyrin conjugate
14. SPPS of the Natural Product Chitinase Inhibitor Argifin: Library Generation and Biological Evaluation
15. Synthesis and Structure-based Dissection of Cyclic Peptide Chitinase Inhibitors: New Leads for Antifungal and Anti-Inflammatory Drugs
16. The cancer chemopreventive actions of phytochemicals derived from glucosinolates
17. Structural Investigations, Cellular Imaging, and Radiolabeling of Neutral, Polycationic, and Polyanionic Functional Metalloporphyrin Conjugates
18. Efficient synthesis of 1,3,7-substituted xanthines by a safety-catch protection strategy
19. Time-dependent inhibitors of trypanothione reductase: Analogues of the spermidine alkaloid lunarine and related natural products
20. Peptide Targeting of Photosensitisers for Photodynamic Therapy and Drug Delivery
21. 1-Cyano-2,3-epithiopropane is a novel plant-derived chemopreventive agent which induces cytoprotective genes that afford resistance against the genotoxic α,β-unsaturated aldehyde acrolein
22. Transcription factor Nrf2 mediates an adaptive response to sulforaphane that protects fibroblasts in vitro against the cytotoxic effects of electrophiles, peroxides and redox-cycling agents
23. An efficient synthesis of 5-aminolaevulinic acid (ALA)-containing peptides for use in photodynamic therapy
24. Specificity of the trypanothione-dependent Leishmania major glyoxalase I: structure and biochemical comparison with the human enzyme
25. Benzofuranyl 3,5-bis-Polyamine derivatives as time-Dependent inhibitors of trypanothione reductase
26. Development of a peptide-based fluorescent probe for biological heme monitoring
27. Cyclo-(L-histidylglycyl-L-prolylglycyl-L-prolylglycine)
28. Solid-phase synthesis of cyclic peptide chitinase inhibitors: SAR of the argifin scaffold† †Electronic supplementary information (ESI) available: ES-MS data for compounds 10a and 10b. See DOI: 10.1039/b815077j Click here for additional data file
29. Endolysosomal targeting of a clinical chlorin photosensitiser for light-triggered delivery of nano-sized medicines
30. Abstract B38: Photochemical internalisation for the local delivery of chemotherapy in prostate cancer
31. The Use of Dipeptide Derivatives of 5-Aminolaevulinic Acid Promotes Their Entry to Tumor Cells and Improves Tumor Selectivity of Photodynamic Therapy
32. A fluorescent Arg–Gly–Asp (RGD) peptide–naphthalenediimide (NDI) conjugate for imaging integrin αvβ3in vitro
33. Bioactive components in foods
34. Fluorescence Lifetime Imaging and FRET‐Induced Intracellular Redistribution of Tat‐Conjugated Quantum Dot Nanoparticles through Interaction with a Phthalocyanine Photosensitiser
35. Quantitative determination of 5-aminolaevulinic acid and its esters in cell lysates by HPLC-fluorescence
36. Human YKL-39 is a pseudo-chitinase with retained chitooligosaccharide-binding properties
37. Analyzing Airway Inflammation with Chemical Biology: Dissection of Acidic Mammalian Chitinase Function with a Selective Drug-like Inhibitor
38. Bisdionin C—A Rationally Designed, Submicromolar Inhibitor of Family 18 Chitinases
39. Natural Product–Guided Discovery of a Fungal Chitinase Inhibitor
40. ChemInform Abstract: Regiocontrolled Synthesis of the Macrocyclic Polyamine Alkaloid (.+-.)-Lunarine, a Time-Dependent Inhibitor of Trypanothione Reductase.
41. Novel prodrug approach to photodynamic therapy: Fmoc solid-phase synthesis of a cell permeable peptide incorporating 5-aminolaevulinic acid
42. Improved Peptide Prodrugs of 5-ALA for PDT: Rationalization of Cellular Accumulation and Protoporphyrin IX Production by Direct Determination of Cellular Prodrug Uptake and Prodrug Metabolization
43. Solid-phase synthesis of cyclic peptide chitinase inhibitors: SAR of the argifin scaffold
44. ChemInform Abstract: Convenient Preparation of N-Maleoyl Amino Acid Succinimido Esters Using N-Trifluoroacetoxysuccinimide.
45. 5-Aminolaevulinic acid peptide prodrugs enhance photosensitization for photodynamic therapy
46. ChemInform Abstract: Efficient Synthesis of 1,3,7‐Substituted Xanthines by a Safety‐Catch Protection Strategy.
47. Structure-Based Dissection of the Natural Product Cyclopentapeptide Chitinase Inhibitor Argifin
48. Convenient Preparation ofN‐Maleoyl Amino Acid Succinimido Esters usingN‐Trifluoroacetoxysuccinimide
49. First Synthesis of Argadin: A Nanomolar Inhibitor of Family-18 Chitinases
50. A fluorescent Arg–Gly–Asp (RGD) peptide–naphthalenediimide (NDI) conjugate for imaging integrin αvβ3in vitro.
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