Development of rhodesain inhibitors with a 3-bromoisoxazoline warhead.
about
Identification of non-peptidic cysteine reactive fragments as inhibitors of cysteine protease rhodesainSynthesis and biological evaluation of papain-family cathepsin L-like cysteine protease inhibitors containing a 1,4-benzodiazepine scaffold as antiprotozoal agents.Development of novel selective peptidomimetics containing a boronic acid moiety, targeting the 20S proteasome as anticancer agents.Inspired by Nature: The 3-Halo-4,5-dihydroisoxazole Moiety as a Novel Molecular Warhead for the Design of Covalent Inhibitors.Effects of 3-Bromo-4,5-dihydroisoxazole Derivatives on Nrf2 Activation and Heme Oxygenase-1 ExpressionSynthesis of unusual isoxazoline containing β and γ-dipeptides as potential glutamate receptor ligandsNMR conformational analysis in solution of a potent class of cysteine proteases inhibitors
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P2860
Development of rhodesain inhibitors with a 3-bromoisoxazoline warhead.
description
2013 nî lūn-bûn
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2013年の論文
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年學術文章
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name
Development of rhodesain inhibitors with a 3-bromoisoxazoline warhead.
@en
Development of rhodesain inhibitors with a 3-bromoisoxazoline warhead.
@nl
type
label
Development of rhodesain inhibitors with a 3-bromoisoxazoline warhead.
@en
Development of rhodesain inhibitors with a 3-bromoisoxazoline warhead.
@nl
prefLabel
Development of rhodesain inhibitors with a 3-bromoisoxazoline warhead.
@en
Development of rhodesain inhibitors with a 3-bromoisoxazoline warhead.
@nl
P2860
P50
P356
P1433
P1476
Development of rhodesain inhibitors with a 3-bromoisoxazoline warhead.
@en
P2093
Ilenia C Angelo
P2860
P304
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10.1002/CMDC.201300390
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P577
2013-11-15T00:00:00Z