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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 JAK2Identification of imidazo-pyrrolopyridines as novel and potent JAK1 inhibitorsStructure-based discovery of C-2 substituted imidazo-pyrrolopyridine JAK1 inhibitors with improved selectivity over JAK2Novel triazolo-pyrrolopyridines as inhibitors of Janus kinase 1Design and evaluation of novel 8-oxo-pyridopyrimidine Jak1/2 inhibitorsScaffold-Hopping and Structure-Based Discovery of Potent, Selective, And Brain Penetrant N-(1H-Pyrazol-3-yl)pyridin-2-amine Inhibitors of Dual Leucine Zipper Kinase (DLK, MAP3K12)Discovery of GluN2A-Selective NMDA Receptor Positive Allosteric Modulators (PAMs): Tuning Deactivation Kinetics via Structure-Based DesignDesign and evaluation of 1,7-naphthyridones as novel KDM5 inhibitors
P50
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P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Gauri Deshmukh
@ast
Gauri Deshmukh
@en
Gauri Deshmukh
@es
Gauri Deshmukh
@nl
Gauri Deshmukh
@sl
type
label
Gauri Deshmukh
@ast
Gauri Deshmukh
@en
Gauri Deshmukh
@es
Gauri Deshmukh
@nl
Gauri Deshmukh
@sl
prefLabel
Gauri Deshmukh
@ast
Gauri Deshmukh
@en
Gauri Deshmukh
@es
Gauri Deshmukh
@nl
Gauri Deshmukh
@sl