Amanote Research
Register
Sign In
Optimization of a Benzoylpiperidine Class Identifies a Highly Potent and Selective Reversible Monoacylglycerol Lipase (MAGL) Inhibitor
doi 10.1021/acs.jmedchem.8b01483.s001
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
Discovery of 1,5-Diphenylpyrazole-3-Carboxamide Derivatives as Potent, Reversible, and Selective Monoacylglycerol Lipase (MAGL) Inhibitors
Journal of Medicinal Chemistry
Drug Discovery
Molecular Medicine
Discovery of 1,5-Diphenylpyrazole-3-Carboxamide Derivatives as Potent, Reversible, and Selective Monoacylglycerol Lipase (MAGL) Inhibitors
Identification of a Potent, Highly Selective, and Brain Penetrant Phosphodiesterase 2A Inhibitor Clinical Candidate
Preclinical Characterization of Anlotinib, a Highly Potent and Selective Vascular Endothelial Growth Factor Receptor-2 Inhibitor
Cancer Science
Cancer Research
Medicine
Oncology
A Novel, Highly Potent and Selective Phosphodiesterase-9 Inhibitor for the Treatment of Sickle Cell Disease
Haematologica
Hematology
Optimization of a Novel Potent and Selective Bacterial DNA Helicase Inhibitor Scaffold From a High Throughput Screening Hit
Bioorganic and Medicinal Chemistry Letters
Organic Chemistry
Molecular Medicine
Molecular Biology
Biochemistry
Clinical Biochemistry
Pharmaceutical Science
Drug Discovery
Conformational Transition Pathway in the Inhibitor Binding Process of Human Monoacylglycerol Lipase
Protein Journal
Biochemistry
Bioengineering
Analytical Chemistry
Organic Chemistry
4-Aryliden-2-Methyloxazol-5(4h)-One as a New Scaffold for Selective Reversible MAGL Inhibitors
Journal of Enzyme Inhibition and Medicinal Chemistry
Medicine
Drug Discovery
Pharmacology
A Comparison of Novel, Selective Fatty Acid Amide Hydrolase (FAAH), Monoacyglycerol Lipase (MAGL) or Dual FAAH/MAGL Inhibitors to Suppress Acute and Anticipatory Nausea in Rat Models
Psychopharmacology
Pharmacology
