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1 bitor previously under clinical development (pleconaril).
2 This density could be displaced by pleconaril.
3 , ribavirin, and the anti-picornaviral agent pleconaril.
5 al structures of EV-D68 and its complex with pleconaril, a capsid-binding compound that had been deve
6 nd study assessed the efficacy and safety of pleconaril, a novel antiviral drug with broad-spectrum a
7 studies showing that the antiviral effect of pleconaril against HRV16 is greater on the infectivity o
9 h small-molecule antiviral compounds such as pleconaril bind and inhibit functions associated with th
10 irus 16 (HRV16) and HRV14 are incubated with pleconaril, drug occupancy in the binding pocket is lowe
11 Other potentially useful treatments, such as pleconaril for enteroviral meningoencephalitis are under
12 hese data support the safety and efficacy of pleconaril in decreasing the signs and symptoms and vira
15 e development of capsid-function inhibitors (pleconaril), inhibitors of 3C protease (AG7088), and rec
18 ncy in the binding pocket is lower than when pleconaril is introduced during assembly prior to crysta
19 s after receiving the initial dose of either pleconaril or placebo, subjects were inoculated intranas
20 he virus developed reduced susceptibility to pleconaril, precluding the in-vivo use of this drug.
24 spiratory illness symptom scores (P=.013) in pleconaril-treated as compared with placebo-treated subj
26 om patients enrolled in clinical trials with pleconaril were distinct from those that confer natural
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