Synthesis of sulfated octadecyl ribo-oligosaccharides with potent anti-AIDS virus activity by ring-opening polymerization of a 1,4-anhydroribose derivative-Reference-Cited by-同舟云学术

Synthesis of sulfated octadecyl ribo-oligosaccharides with potent anti-AIDS virus activity by ring-opening polymerization of a 1,4-anhydroribose derivative

Published:1996-02 Issue:1 Volume:282 Page:113-123
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Choi YoonSoung,Yoshida Takashi,Mimura Toru,Kaneko Yutaro,Nakashima Hideki,Yamamoto Naoki,Uryu Toshiyuki

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference17 articles.

1. Artificial polysaccharides and their biological activities

2. Synthesis of branched ribofuranans and their sulfates with strong anti-AIDS virus activity by selective ring-opening copolymerization of 1,4-anhydro-α-D-ribopyranose derivatives.

3. Synthesis of Cellulose-Type Polyriboses and Their Branched Sulfates with Anti-AIDS Virus Activity by Selective Ring-Opening Copolymerization of 1,4-Anhydro-.alpha.-D-ribopyranose Derivatives

4. Synthesis and structural analysis of curdlan sulfate with a potent inhibitory effect in vitro of AIDS virus infection

5. Inhibition of HIV-1 infectivity with curdlan sulfate in vitro

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