1362692-50-9Relevant academic research and scientific papers
Fluorine-18 and carbon-11 labeled radioligands for positron emission tomography (PET) imaging for LRRK2
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Page/Page column 75, (2015/11/16)
A method for positron emission tomography (PET) imaging of LRRK2 in tissue of a subject, the method comprising: administering a compound of formula I, formula II or formula III, or a pharmaceutically acceptable salt thereof to the subject, wherein the com
FLUORINE-18 AND CARBON-11 LABELED RADIOLIGANDS FOR POSITRON EMISSION TOMOGRAPHY (PET) IMAGING FOR LRRK2
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Page/Page column 120-121, (2013/06/27)
A method for positron emission tomography (PET) imaging of LRRK2 in the tissue of a subject, the method comprising: administering a compound of formula (I), formula (II) or formula (III), or a pharmaceutically acceptable salt thereof to the subject, where
Discovery of highly potent, selective, and brain-penetrable leucine-rich repeat kinase 2 (LRRK2) small molecule inhibitors
Estrada, Anthony A.,Liu, Xingrong,Baker-Glenn, Charles,Beresford, Alan,Burdick, Daniel J.,Chambers, Mark,Chan, Bryan K.,Chen, Huifen,Ding, Xiao,Dipasquale, Antonio G.,Dominguez, Sara L.,Dotson, Jennafer,Drummond, Jason,Flagella, Michael,Flynn, Sean,Fuji, Reina,Gill, Andrew,Gunzner-Toste, Janet,Harris, Seth F.,Heffron, Timothy P.,Kleinheinz, Tracy,Lee, Donna W.,Le Pichon, Claire E.,Lyssikatos, Joseph P.,Medhurst, Andrew D.,Moffat, John G.,Mukund, Susmith,Nash, Kevin,Scearce-Levie, Kimberly,Sheng, Zejuan,Shore, Daniel G.,Tran, Thuy,Trivedi, Naimisha,Wang, Shumei,Zhang, Shuo,Zhang, Xiaolin,Zhao, Guiling,Zhu, Haitao,Sweeney, Zachary K.
, p. 9416 - 9433 (2013/01/16)
There is a high demand for potent, selective, and brain-penetrant small molecule inhibitors of leucine-rich repeat kinase 2 (LRRK2) to test whether inhibition of LRRK2 kinase activity is a potentially viable treatment option for Parkinson's disease patients. Herein we disclose the use of property and structure-based drug design for the optimization of highly ligand efficient aminopyrimidine lead compounds. High throughput in vivo rodent cassette pharmacokinetic studies enabled rapid validation of in vitro-in vivo correlations. Guided by this data, optimal design parameters were established. Effective incorporation of these guidelines into our molecular design process resulted in the discovery of small molecule inhibitors such as GNE-7915 (18) and 19, which possess an ideal balance of LRRK2 cellular potency, broad kinase selectivity, metabolic stability, and brain penetration across multiple species. Advancement of GNE-7915 into rodent and higher species toxicity studies enabled risk assessment for early development.
