Discovery of highly potent, selective, and brain-penetrable leucine-rich repeat kinase 2 (LRRK2) small molecule inhibitors.
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LRRK2 kinase activity and biology are not uniformly predicted by its autophosphorylation and cellular phosphorylation site statusHeterogeneity of leucine-rich repeat kinase 2 mutations: genetics, mechanisms and therapeutic implicationsStructure-Based Design of Orally Bioavailable 1 H -Pyrrolo[3,2- c ]pyridine Inhibitors of Mitotic Kinase Monopolar Spindle 1 (MPS1)LRRK2 inhibitors and their potential in the treatment of Parkinson's disease: current perspectivesGenetic and pharmacological evidence that G2019S LRRK2 confers a hyperkinetic phenotype, resistant to motor decline associated with aging.Kinase drug discovery--what's next in the field?A small molecule bidentate-binding dual inhibitor probe of the LRRK2 and JNK kinases.Discovery of a Pyrrolopyrimidine (JH-II-127), a Highly Potent, Selective, and Brain Penetrant LRRK2 Inhibitor.Altered Development of Synapse Structure and Function in Striatum Caused by Parkinson's Disease-Linked LRRK2-G2019S MutationEffects of LRRK2 Inhibitors on Nigrostriatal Dopaminergic NeurotransmissionDual leucine zipper kinase as a therapeutic target for neurodegenerative conditions.LRRK2, a puzzling protein: insights into Parkinson's disease pathogenesisLeucine-rich repeat kinase 2 inhibitors: a review of recent patents (2011 - 2013).LRRK2 Kinase Inhibition as a Therapeutic Strategy for Parkinson's Disease, Where Do We Stand?Fluorine-18 patents (2009-2015). Part 1: novel radiotracers.GTP binding regulates cellular localization of Parkinson's disease-associated LRRK2.Novel 2,4-dianilino-5-fluoropyrimidine derivatives possessing ALK inhibitory activities.Targeting LRRK2 in Parkinson's disease: an update on recent developments.Discovery of a Highly Selective, Brain-Penetrant Aminopyrazole LRRK2 Inhibitor.Phosphoproteomic evaluation of pharmacological inhibition of leucine-rich repeat kinase 2 reveals significant off-target effects of LRRK-2-IN-1.Effect of selective LRRK2 kinase inhibition on nonhuman primate lung.A homologue of the Parkinson's disease-associated protein LRRK2 undergoes a monomer-dimer transition during GTP turnover.Synthesis and In Vitro and In Vivo Evaluation of [3H]LRRK2-IN-1 as a Novel Radioligand for LRRK2.Small-Molecule Inhibitors of LRRK2.The dual enzyme LRRK2 hydrolyzes GTP in both its GTPase and kinase domains in vitro.An integrated suite of modeling tools that empower scientists in structure- and property-based drug design.
P2860
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P2860
Discovery of highly potent, selective, and brain-penetrable leucine-rich repeat kinase 2 (LRRK2) small molecule inhibitors.
description
2012 nî lūn-bûn
@nan
2012 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Discovery of highly potent, se ...... K2) small molecule inhibitors.
@ast
Discovery of highly potent, se ...... K2) small molecule inhibitors.
@en
Discovery of highly potent, se ...... K2) small molecule inhibitors.
@nl
type
label
Discovery of highly potent, se ...... K2) small molecule inhibitors.
@ast
Discovery of highly potent, se ...... K2) small molecule inhibitors.
@en
Discovery of highly potent, se ...... K2) small molecule inhibitors.
@nl
prefLabel
Discovery of highly potent, se ...... K2) small molecule inhibitors.
@ast
Discovery of highly potent, se ...... K2) small molecule inhibitors.
@en
Discovery of highly potent, se ...... K2) small molecule inhibitors.
@nl
P2093
P356
P1476
Discovery of highly potent, se ...... K2) small molecule inhibitors.
@en
P2093
Alan Beresford
Andrew D Medhurst
Andrew Gill
Anthony A Estrada
Antonio G DiPasquale
Bryan K Chan
Charles Baker-Glenn
Claire E Le Pichon
Daniel G Shore
Daniel J Burdick
P304
P356
10.1021/JM301020Q
P407
P577
2012-10-15T00:00:00Z