about
Identification of C-2 hydroxyethyl imidazopyrrolopyridines as potent JAK1 inhibitors with favorable physicochemical properties and high selectivity over JAK2Discovery and optimization of C-2 methyl imidazopyrrolopyridines as potent and orally bioavailable JAK1 inhibitors with selectivity over JAK2Structure-based discovery of C-2 substituted imidazo-pyrrolopyridine JAK1 inhibitors with improved selectivity over JAK2Identification of substituted 2-thio-6-oxo-1,6-dihydropyrimidines as inhibitors of human lactate dehydrogenaseIdentification of 2-amino-5-aryl-pyrazines as inhibitors of human lactate dehydrogenaseDesign and evaluation of novel 8-oxo-pyridopyrimidine Jak1/2 inhibitorsIdentification of substituted 3-hydroxy-2-mercaptocyclohex-2-enones as potent inhibitors of human lactate dehydrogenaseOptimization of 5-(2,6-dichlorophenyl)-3-hydroxy-2-mercaptocyclohex-2-enones as potent inhibitors of human lactate dehydrogenaseIdentification of 3,6-disubstituted dihydropyrones as inhibitors of human lactate dehydrogenaseMetabolic plasticity underpins innate and acquired resistance to LDHA inhibition
P50
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P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Sharada Labadie
@ast
Sharada Labadie
@en
Sharada Labadie
@es
Sharada Labadie
@sl
type
label
Sharada Labadie
@ast
Sharada Labadie
@en
Sharada Labadie
@es
Sharada Labadie
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prefLabel
Sharada Labadie
@ast
Sharada Labadie
@en
Sharada Labadie
@es
Sharada Labadie
@sl