Open saccharin-based secondary sulfonamides as potent and selective inhibitors of cancer-related carbonic anhydrase IX and XII isoforms.
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N-Acylbenzenesulfonamide Dihydro-1,3,4-oxadiazole Hybrids: Seeking Selectivity toward Carbonic Anhydrase Isoforms.Potent and Selective Carboxylic Acid Inhibitors of Tumor-Associated Carbonic Anhydrases IX and XII.Design, Synthesis, Molecular Docking Analysis, and Carbonic Anhydrase IX Inhibitory Evaluations of Novel N-Substituted-β-d-Glucosamine Derivatives that Incorporate Benzenesulfonamides.Novel thiazolidinone-containing compounds, without the well-known sulphonamide zinc-binding group acting as human carbonic anhydrase IX inhibitors
P2860
Open saccharin-based secondary sulfonamides as potent and selective inhibitors of cancer-related carbonic anhydrase IX and XII isoforms.
description
2016 nî lūn-bûn
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2016年の論文
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2016年学术文章
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2016年学术文章
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2016年学术文章
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2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
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2016年學術文章
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2016年學術文章
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name
Open saccharin-based secondary ...... anhydrase IX and XII isoforms.
@en
Open saccharin-based secondary ...... anhydrase IX and XII isoforms.
@nl
type
label
Open saccharin-based secondary ...... anhydrase IX and XII isoforms.
@en
Open saccharin-based secondary ...... anhydrase IX and XII isoforms.
@nl
prefLabel
Open saccharin-based secondary ...... anhydrase IX and XII isoforms.
@en
Open saccharin-based secondary ...... anhydrase IX and XII isoforms.
@nl
P2093
P2860
P50
P1476
Open saccharin-based secondary ...... anhydrase IX and XII isoforms
@en
P2093
Anatoly P Sobolev
Claudiu T Supuran
Daniela Secci
Mariangela Ceruso
Melissa D'Ascenzio
Rosalba Florio
P2860
P356
10.1080/14756366.2016.1235040
P577
2016-10-26T00:00:00Z