scholarly article | Q13442814 |
P2093 | author name string | W Li | |
L Zhang | |||
M Williams | |||
C U Kim | |||
D B Mendel | |||
E J Eisenberg | |||
M S Chen | |||
N Bischofberger | |||
P A Escarpe | |||
C Sweet | |||
K C Cundy | |||
W Lew | |||
K J Jakeman | |||
J Merson | |||
P2860 | cites work | Influenza type A virus neuraminidase does not play a role in viral entry, replication, assembly, or budding | Q24676721 |
Characterization of temperature sensitive influenza virus mutants defective in neuraminidase | Q27865285 | ||
Inhibition of influenza virus replication in tissue culture by 2-deoxy-2,3-dehydro-N-trifluoroacetylneuraminic acid (FANA): mechanism of action | Q27867721 | ||
Inhibition of influenza virus replication in mice by GG167 (4-guanidino-2,4-dideoxy-2,3-dehydro-N-acetylneuraminic acid) is consistent with extracellular activity of viral neuraminidase (sialidase) | Q28368367 | ||
4-Guanidino-2,4-dideoxy-2,3-dehydro-N-acetylneuraminic acid is a highly effective inhibitor both of the sialidase (neuraminidase) and of growth of a wide range of influenza A and B viruses in vitro | Q28378588 | ||
Oral administration of a prodrug of the influenza virus neuraminidase inhibitor GS 4071 protects mice and ferrets against influenza infection | Q28379409 | ||
Rational design of potent sialidase-based inhibitors of influenza virus replication | Q29616647 | ||
Emergence and transmission of influenza A viruses resistant to amantadine and rimantadine | Q30437341 | ||
Safety and efficacy of the neuraminidase inhibitor GG167 in experimental human influenza | Q30467966 | ||
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Prodrugs. Do they have advantages in clinical practice? | Q34193849 | ||
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Influenza neuraminidase inhibitors possessing a novel hydrophobic interaction in the enzyme active site: design, synthesis, and structural analysis of carbocyclic sialic acid analogues with potent anti-influenza activity | Q34565520 | ||
GG167 (4-guanidino-2,4-dideoxy-2,3-dehydro-N-acetylneuraminic acid) is a potent inhibitor of influenza virus in ferrets | Q35120465 | ||
Penetration of GS4071, a novel influenza neuraminidase inhibitor, into rat bronchoalveolar lining fluid following oral administration of the prodrug GS4104. | Q35138108 | ||
The molecular biology of influenza virus pathogenicity | Q39520174 | ||
Resistance of influenza A virus to amantadine and rimantadine: results of one decade of surveillance | Q40777039 | ||
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Influenza virus neuraminidase with hemagglutinin activity | Q41420817 | ||
Fluorometric assay of neuraminidase with a sodium (4-methylumbelliferyl-alpha-D-N-acetylneuraminate) substrate | Q41720424 | ||
First-pass uptake of verapamil, diazepam, and thiopental in the human lung | Q45387856 | ||
Mucins and mucoids in relation to influenza virus action; inhibition by purified mucoid of infection and haemagglutination with the virus strain WSE. | Q45390019 | ||
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Species differences in the stereoselective hydrolysis of esmolol by blood esterases | Q69922841 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P1104 | number of pages | 7 | |
P304 | page(s) | 647-653 | |
P577 | publication date | 1998-03-01 | |
P1433 | published in | Antimicrobial Agents and Chemotherapy | Q578004 |
P1476 | title | Identification of GS 4104 as an orally bioavailable prodrug of the influenza virus neuraminidase inhibitor GS 4071. | |
P478 | volume | 42 |
Q34714853 | Animal Models for Influenza Virus Pathogenesis and Transmission |
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