Synthesis of mono-glucose-branched cyclodextrins with a high inclusion ability for doxorubicin and their efficient glycosylation using Mucor hiemalis endo-β-N-acetylglucosaminidase-Reference-Cited by-同舟云学术

Synthesis of mono-glucose-branched cyclodextrins with a high inclusion ability for doxorubicin and their efficient glycosylation using Mucor hiemalis endo-β-N-acetylglucosaminidase

Published:2005-02 Issue:4 Volume:15 Page:1009-1013
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Yamanoi Takashi,Yoshida Naomichi,Oda Yoshiki,Akaike Eri,Tsutsumida Maki,Kobayashi Natsumi,Osumi Kenji,Yamamoto Kenji,Fujita Kiyotaka,Takahashi Keiko,Hattori Kenjiro

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference26 articles.

1. Preparation and Characterization of 61,6n-DI-O-(α-D-Galactopyranosyl)Cyclomaltooctaoses

2. A Highly Practical Synthesis of Cyclodextrin-Based Glycoclusters Having Enhanced Affinity with Lectins

3. Synthesis of Cyclodextrin Derivatives Carrying Bio-Recognisable Saccharide Antennae

4. Synthesis and comparative lectin-binding affinity of mannosyl-coated β-cyclodextrin-dendrimer constructs

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