23 articles for thisTarget

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The following articles (labelled with PubMed ID or TBD) are for your review

PMID	Data	Article Title	Organization
28112927	34	Selective Inhibitors of Human Liver Carboxylesterase Based on aß-Lapachone Scaffold: Novel Reagents for Reaction Profiling.	St. Jude Children'S Research Hospital
26900660	35	Design, synthesis, and structure-activity relationship study of glycyrrhetinic acid derivatives as potent and selective inhibitors against human carboxylesterase 2.	Dalian Institute of Chemical Physics
23386702	10	Reversible inhibition of human carboxylesterases by acyl glucuronides.	Eisai
23286284	50	Modulation of esterified drug metabolism by tanshinones from Salvia miltiorrhiza ("Danshen").	St. Jude Children'S Research Hospital
19062296	63	Comparison of benzil and trifluoromethyl ketone (TFK)-mediated carboxylesterase inhibition using classical and 3D-quantitative structure-activity relationship analysis.	Kyoto University
19534556	57	Improved, selective, human intestinal carboxylesterase inhibitors designed to modulate 7-ethyl-10-[4-(1-piperidino)-1-piperidino]carbonyloxycamptothecin (Irinotecan; CPT-11) toxicity.	St. Jude Children'S Research Hospital
18630870	236	Optimization of the central heterocycle of alpha-ketoheterocycle inhibitors of fatty acid amide hydrolase.	Institute For Chemical Biology
18247553	174	Optimization of alpha-ketooxazole inhibitors of fatty acid amide hydrolase.	The Scripps Research Institute
18023188	86	Influence of sulfur oxidation state and steric bulk upon trifluoromethyl ketone (TFK) binding kinetics to carboxylesterases and fatty acid amide hydrolase (FAAH).	University of California
17279740	191	Potent and selective alpha-ketoheterocycle-based inhibitors of the anandamide and oleamide catabolizing enzyme, fatty acid amide hydrolase.	The Scripps Research Institute
21733699	121	Requirements for mammalian carboxylesterase inhibition by substituted ethane-1,2-diones.	St. Jude Children'S Research Hospital
21105730	30	Structure-activity relationships of substituted 1-pyridyl-2-phenyl-1,2-ethanediones: potent, selective carboxylesterase inhibitors.	St. Jude Children'S Research Hospital
18639454	55	Exploration of a fundamental substituent effect of alpha-ketoheterocycle enzyme inhibitors: Potent and selective inhibitors of fatty acid amide hydrolase.	The Scripps Research Institute
17399985	136	Analysis of the inhibition of mammalian carboxylesterases by novel fluorobenzoins and fluorobenzils.	St. Jude Children'S Research Hospital
16107154	41	Inhibition of carboxylesterases by benzil (diphenylethane-1,2-dione) and heterocyclic analogues is dependent upon the aromaticity of the ring and the flexibility of the dione moiety.	St. Jude Children'S Research Hospital
15771430	129	Discovery of a potent, selective, and efficacious class of reversible alpha-ketoheterocycle inhibitors of fatty acid amide hydrolase effective as analgesics.	The Scripps Research Institute
15713400	99	Discovery of an exceptionally potent and selective class of fatty acid amide hydrolase inhibitors enlisting proteome-wide selectivity screening: concurrent optimization of enzyme inhibitor potency and selectivity.	The Scripps Research Institute
21168763	9	Natural product-guided discovery of a fungal chitinase inhibitor.	University of Dundee