Synthetic sialic-acid-containing polyvalent antiviral inhibitors

被引:21
作者
Carlescu, Irina [1 ]
Scutaru, Dan [1 ]
Popa, Marcel [1 ]
Uglea, Constantin V. [2 ]
机构
[1] Gh Asachi Tech Univ, Fac Chem Engn & Environm Protect, Dept Nat & Synthet Polymers, Iasi 700050, Romania
[2] Gr T Popa Univ Med & Pharm Iasi, Fac Biomed Engn, Iasi, Romania
关键词
Polyvalent synthetic inhibitors; Glycoconjugates; Influenza virus; Sialic acid; Antiviral properties; INFLUENZA-A VIRUS; HEMAGGLUTININ MEMBRANE GLYCOPROTEIN; CONJUGATED DENDRITIC POLYMERS; RECEPTOR-BINDING ACTIVITY; CHEMICAL-MODIFICATION; RNA INTERFERENCE; SIALOSIDE GROUPS; CHEMOENZYMATIC SYNTHESIS; AVIAN INFLUENZA; MULTIVALENT SIALYLOLIGOSACCHARIDES;
D O I
10.1007/s00044-008-9139-7
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
This review gives a brief survey of synthetic inhibitors of influenza virus which have been synthesized to date. It starts with a short introduction which describes the structure and mechanism of action of influenza virus and continues with the main research directions that have been used in order to inhibit the virus. This is followed by discussion of various synthetic materials, including synthesis and antiviral properties, which that have been tested against influenza virus. The most potent inhibitory compounds proved to be polyvalent, because of their high binding affinity and steric stabilization. Finally we conclude with a brief discussion on structural characteristics, a summary, and outlook overview.
引用
收藏
页码:477 / 494
页数:18
相关论文
共 94 条
[1]  
Al-Majhdi F. N., 2007, Journal of Biological Sciences, V7, P113
[2]   Probing the receptor interactions ofan H5 avian influenza virus using a baculovirus expression system and functionalised poly(acrylic acid) ligands [J].
Barclay, Wendy S. ;
Jones, Ian M. ;
Osborn, Helen M. I. ;
Phillipson, Louisa ;
Ren, Junyuan ;
Talevera, Guadalupe A. ;
Thompson, Catherine I. .
BIOORGANIC & MEDICINAL CHEMISTRY, 2007, 15 (12) :4038-4047
[3]   Current and future antiviral therapy of severe seasonal and avian influenza [J].
Beigel, John ;
Bray, Mike .
ANTIVIRAL RESEARCH, 2008, 78 (01) :91-102
[4]   RESISTANCE OF INFLUENZA-A VIRUS TO AMANTADINE AND RIMANTADINE - RESULTS OF ONE DECADE OF SURVEILLANCE [J].
BELSHE, RB ;
BURK, B ;
NEWMAN, F ;
CERRUTI, RL ;
SIM, IS .
JOURNAL OF INFECTIOUS DISEASES, 1989, 159 (03) :430-435
[5]   Multimeric glycotherapeutics: New paradigm [J].
Bovin, NV ;
Tuzikov, AB ;
Chinarev, AA ;
Gambaryan, AS .
GLYCOCONJUGATE JOURNAL, 2004, 21 (8-9) :471-478
[6]   Polyacrylamide-based glycoconjugates as tools in glycobiology [J].
Bovin, NV .
GLYCOCONJUGATE JOURNAL, 1998, 15 (05) :431-446
[7]   SYNTHESIS OF POLYMERIC NEOGLYCOCONJUGATES BASED ON N-SUBSTITUTED POLYACRYLAMIDES [J].
BOVIN, NV ;
KORCHAGINA, EY ;
ZEMLYANUKHINA, TV ;
BYRAMOVA, NE ;
GALANINA, OE ;
ZEMLYAKOV, AE ;
IVANOV, AE ;
ZUBOV, VP ;
MOCHALOVA, LV .
GLYCOCONJUGATE JOURNAL, 1993, 10 (02) :142-151
[8]   A 'litmus test' for molecular recognition using artificial membranes [J].
Charych, D ;
Cheng, Q ;
Reichert, A ;
Kuziemko, G ;
Stroh, M ;
Nagy, JO ;
Spevak, W ;
Stevens, RC .
CHEMISTRY & BIOLOGY, 1996, 3 (02) :113-120
[9]  
CHIN A, 1999, S VLSI, P135, DOI DOI 10.1109/VLSIT.1999.799380
[10]   Monomeric inhibitors of influenza neuraminidase enhance the hemagglutination inhibition activities of polyacrylamides presenting multiple C-sialoside groups [J].
Choi, SK ;
Mammen, M ;
Whitesides, GM .
CHEMISTRY & BIOLOGY, 1996, 3 (02) :97-104