Synthesis, structure, and evaluation of a β-cyclodextrin-artificial carbohydrate conjugate for use as a doxorubicin-carrying molecule
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry
Reference20 articles.
1. A review of glycosylated carriers for drug delivery
2. Multivalent Cyclooligosaccharides: Versatile Carbohydrate Clusters with Dual Role as Molecular Receptors and Lectin Ligands
3. Synthesis of mono-glucose-branched cyclodextrins with a high inclusion ability for doxorubicin and their efficient glycosylation using Mucor hiemalis endo-β-N-acetylglucosaminidase
4. Preparation of a Cyclodextrin Conjugated With Two Arbutin Moieties as a Drug-Carrier Model, and its High Ability for the Inclusion of Doxorubicin
5. β-Cyclodextrin Conjugates with Glucose Moieties Designed as Drug Carriers: Their Syntheses, Evaluations Using Concanavalin A and Doxorubicin, and Structural Analyses by NMR Spectroscopy
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1. A Synthetic Approach for Hepta-Branched β-Cyclodextrins Bearing Heterogeneous Carbohydrate Residues at Their Primary Side via a One-Pot Process with a Simultaneous Click Chemistry Reaction;Synlett;2023-11-01
2. Carbohydrate–macrocycle conjugates for biomedical applications;Materials Chemistry Frontiers;2023
3. β and γ-Cyclodextrin dimers: design, characterization and in silico studies to explore the cooperative effect of the cavities;New Journal of Chemistry;2023
4. Synthesis of Hepta-arbutin-branched β-Cyclodextrins at Their Primary Sides via Click Reaction;HETEROCYCLES;2023
5. Multifunctional P450 Monooxygenase CftA Diversifies the Clifednamide Pool through Tandem C–H Bond Activations;Journal of Natural Products;2022-01-04
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