Synthesis and in vitro study of novel borneol derivatives as potent inhibitors of the influenza A virus
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Herein, we present the design and synthesis of a series of novel heterocyclic derivatives of (−)-borneol and (−)-isoborneol as potent inhibitors of the influenza A virus.
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1988 ◽
pp. 186-189
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2006 ◽
Vol 38
(8)
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pp. 1382-1392
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2005 ◽
Vol 15
(17)
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pp. 3953-3956
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2019 ◽
Vol 9
(3)
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pp. 2886-2893
1998 ◽
Vol 5
(1)
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pp. 86A-86A