Design, synthesis, anti-schistosomal activity and molecular docking of novel 8-hydroxyquinoline-5-sufonyl 1,4-diazepine derivatives.
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A novel ent-kaurane diterpenoid executes antitumor function in colorectal cancer cells by inhibiting Wnt/β-catenin signaling.Current drug targets for helminthic diseases.In vivo schistosomicidal activity of three novels 8-hydroxyquinoline derivatives against adult and immature worms of Schistosoma mansoni.
P2860
Design, synthesis, anti-schistosomal activity and molecular docking of novel 8-hydroxyquinoline-5-sufonyl 1,4-diazepine derivatives.
description
2012 nî lūn-bûn
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2012年の論文
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年学术文章
@zh-sg
2012年學術文章
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2012年學術文章
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2012年學術文章
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name
Design, synthesis, anti-schist ...... nyl 1,4-diazepine derivatives.
@en
Design, synthesis, anti-schist ...... nyl 1,4-diazepine derivatives.
@nl
type
label
Design, synthesis, anti-schist ...... nyl 1,4-diazepine derivatives.
@en
Design, synthesis, anti-schist ...... nyl 1,4-diazepine derivatives.
@nl
prefLabel
Design, synthesis, anti-schist ...... nyl 1,4-diazepine derivatives.
@en
Design, synthesis, anti-schist ...... nyl 1,4-diazepine derivatives.
@nl
P50
P1433
P1476
Design, synthesis, anti-schist ...... onyl 1,4-diazepine derivatives
@en
P2093
Abdul Hamid ALGhamdi
Ibrahim A Maghrabi
P356
10.1016/J.BIOORG.2012.10.003
P577
2012-11-08T00:00:00Z