Neuraminidase inhibitors as antivirals

被引:18
作者
Colman, PM [1 ]
机构
[1] PO Royal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Melbourne, Vic 3050, Australia
关键词
neuraminidase; antivirals; influenza virus;
D O I
10.1016/S0264-410X(02)00132-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The description of the three-dimensional structure of the influenza virus neuraminidase in 1983 opened a new phase in the search for inhibitors of the enzyme. Two compounds in late development (February 1999) have similar levels of potency against influenza A viruses, different routes of administration and, surprisingly, different resistance profiles both in vitro and in vivo. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:S55 / S58
页数:4
相关论文
共 25 条
[11]   Mutations in a conserved residue in the influenza virus neuraminidase active site decreases sensitivity to Neu5Ac2en-derived inhibitors [J].
McKimm-Breschkin, JL ;
Sahasrabudhe, A ;
Blick, TJ ;
McDonald, M ;
Colman, PM ;
Hart, GJ ;
Bethell, RC ;
Varghese, JN .
JOURNAL OF VIROLOGY, 1998, 72 (03) :2456-2462
[12]   Generation and characterization of variants of NWS/G70C influenza virus after in vitro passage in 4-amino-Neu5Ac2en and 4-guanidino-Neu5Ac2en [J].
McKimmBreschkin, JL ;
Blick, TJ ;
Sahasrabudhe, A ;
Tiong, T ;
Marshall, D ;
Hart, GJ ;
Bethell, RC ;
Penn, CR .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (01) :40-46
[13]   INHIBITION OF NEURAMINIDASE ACTIVITY BY DERIVATIVES OF 2-DEOXY-2,3-DEHYDRO-N-ACETYLNEURAMINIC ACID [J].
MEINDL, P ;
BODO, G ;
PALESE, P ;
SCHULMAN, J ;
TUPPY, H .
VIROLOGY, 1974, 58 (02) :457-463
[14]   2-DEOXY-2.3-DEHYDRO-SIALIC ACIDS .I. SYNTHESIS AND PROPERTIES OF 2-DEOXY-2.3-DEHYDRO-N-ACYL-NEURAMINIC ACIDS AND THEIR METHYL ESTERS [J].
MEINDL, P ;
TUPPY, H .
MONATSHEFTE FUR CHEMIE, 1969, 100 (04) :1295-&
[15]   INHIBITION OF INFLUENZA-VIRUS REPLICATION IN TISSUE-CULTURE BY 2-DEOXY-2,3-DEHYDRO-N-TRIFLUOROACETYLNEURAMINIC ACID (FANA) - MECHANISM OF ACTION [J].
PALESE, P ;
COMPANS, RW .
JOURNAL OF GENERAL VIROLOGY, 1976, 33 (OCT) :159-163
[16]  
PALESE P, 1977, CHEMOPROPHYLAXIS VIR, V1, P189
[17]  
SILAGY CA, 1988, LANCET, V352, P1877
[18]   Novel inhibitors of influenza sialidases related to GG167 - Structure-activity, crystallographic and molecular dynamic studies with 4H-pyran-2-carboxylic acid 6-carboxamides [J].
Smith, PW ;
Sollis, SL ;
Howes, PD ;
Cherry, PC ;
Cobley, KN ;
Taylor, H ;
Whittington, AR ;
Scicinski, J ;
Bethell, RC ;
Taylor, N ;
Skarzynski, T ;
Cleasby, A ;
Singh, O ;
Wonacott, A ;
Varghese, J ;
Colman, P .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1996, 6 (24) :2931-2936
[19]   Novel inhibitors of influenza sialidase related to GG167 - Synthesis of 4-amino and guanidino-4H-pyran-2-carboxylic acid-6-propylamides; Selective inhibitors of influenza A virus sialidase [J].
Sollis, SL ;
Smith, PW ;
Howes, PD ;
Cherry, PC ;
Bethell, RC .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1996, 6 (15) :1805-1808
[20]   Dihydropyrancarboxamides related to zanamivir:: A new series of inhibitors of influenza virus sialidases.: 2.: Crystallographic and molecular modeling study of complexes of 4-amino-4H-pyran-6-carboxamides and sialidase from influenza virus types A and B [J].
Taylor, NR ;
Cleasby, A ;
Singh, O ;
Skarzynski, T ;
Wonacott, AJ ;
Smith, PW ;
Sollis, SL ;
Howes, PD ;
Cherry, PC ;
Bethell, R ;
Colman, P ;
Varghese, J .
JOURNAL OF MEDICINAL CHEMISTRY, 1998, 41 (06) :798-807