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Journal of the American Chemical Society|September 28, 2022
Targeted Protein Degradation by Electrophilic PROTACs that Stereoselectively and Site-Specifically Engage DCAF1Yongfeng Tao, David Remillard, Ekaterina V Vinogradova, et al.
SLAS Technology|June 15, 2019
Quantification of In Vivo Target Engagement Using Microfluidic Activity-Based Protein ProfilingHolly T Reardon, Rachel A Herbst, Cassandra L Henry, et al.
ACS Chemical Biology|May 7, 2015
Activity-Based Protein Profiling of Oncogene-Driven Changes in Metabolism Reveals Broad Dysregulation of PAFAH1B2 and 1B3 in CancerRebecca A Kohnz, Melinda M Mulvihill, Jae Won Chang, et al.
Neuropharmacology|June 2, 2020
Inhibition of monoacylglycerol lipase reduces nicotine reward in the conditioned place preference test in male micePretal P Muldoon, Lois S Akinola, Joel E Schlosburg, et al.
Cannabis and Cannabinoid Research|June 18, 2021
Diacylglycerol Lipase-β Knockout Mice Display a Sex-Dependent Attenuation of Traumatic Brain Injury-Induced Mortality with No Impact on Memory or Other Functional ConsequencesLesley D O'Brien, Terry L Smith, Giulia Donvito, et al.
Addiction Biology|June 30, 2017
Fatty acid amide hydrolase (FAAH) inactivation confers enhanced sensitivity to nicotine-induced dopamine release in the mouse nucleus accumbensFrancisco J Pavon, Antonia Serrano, Nimish Sidhpura, et al.
Neuropharmacology|November 29, 2016
The endocannabinoid hydrolysis inhibitor SA-57: Intrinsic antinociceptive effects, augmented morphine-induced antinociception, and attenuated heroin seeking behavior in miceJenny L Wilkerson, Sudeshna Ghosh, Mohammed Mustafa, et al.
Chemical Communications (Cambridge, England)|August 27, 2010
A fluopol-ABPP HTS assay to identify PAD inhibitorsBryan Knuckley, Justin E Jones, Daniel A Bachovchin, et al.
Bioorganic & Medicinal Chemistry Letters|October 19, 2021
Chemical proteomic analysis of palmostatin beta-lactone analogs that affect N-Ras palmitoylationRadu M Suciu, Irungu K Luvaga, Akram Hazeen, et al.
Journal of the American Chemical Society|April 16, 2013
Rational design of fatty acid amide hydrolase inhibitors that act by covalently bonding to two active site residuesKaterina Otrubova, Monica Brown, Michael S McCormick, et al.
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