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European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|September 23, 2015
Antidepressant-like activity and cardioprotective effects of fatty acid amide hydrolase inhibitor URB694 in socially stressed Wistar Kyoto ratsLuca Carnevali, Federica Vacondio, Stefano Rossi, et al.Chemistry & Biology|May 23, 2015
Peroxide-Dependent MGL Sulfenylation Regulates 2-AG-Mediated Endocannabinoid Signaling in Brain NeuronsEmmanuel Y Dotsey, Kwang-Mook Jung, Abdul Basit, et al.Pharmaceuticals (Basel, Switzerland)|January 21, 2022
Metabolic Soft Spot and Pharmacokinetics: Functionalization of C-3 Position of an Eph-Ephrin Antagonist Featuring a Bile Acid Core as an Effective Strategy to Obtain Oral Bioavailability in MiceFrancesca Ferlenghi, Carmine Giorgio, Matteo Incerti, et al.Journal of Medicinal Chemistry|May 4, 2016
Synthesis, Structural Elucidation, and Biological Evaluation of NSC12, an Orally Available Fibroblast Growth Factor (FGF) Ligand Trap for the Treatment of FGF-Dependent Lung TumorsRiccardo Castelli, Arianna Giacomini, Mattia Anselmi, et al.Chemmedchem|May 16, 2014
3-Aminoazetidin-2-one derivatives as N-acylethanolamine acid amidase (NAAA) inhibitors suitable for systemic administrationAnnalisa Fiasella, Andrea Nuzzi, Maria Summa, et al.Bioorganic & Medicinal Chemistry Letters|January 9, 2009
Synthesis and characterization of a peripherally restricted CB1 cannabinoid antagonist, URB447, that reduces feeding and body-weight gain in miceJesse LoVerme, Andrea Duranti, Andrea Tontini, et al.Journal of Medicinal Chemistry|April 26, 2013
Discovery of a new class of highly potent inhibitors of acid ceramidase: synthesis and structure-activity relationship (SAR)Daniela Pizzirani, Chiara Pagliuca, Natalia Realini, et al.Angiogenesis|October 15, 2017
N-tert-butyloxycarbonyl-Phe-Leu-Phe-Leu-Phe (BOC2) inhibits the angiogenic activity of heparin-binding growth factorsImtiaz M Nawaz, Paola Chiodelli, Sara Rezzola, et al.Bioorganic & Medicinal Chemistry|July 22, 2011
Bivalent ligand approach on N-{2-[(3-methoxyphenyl)methylamino]ethyl}acetamide: synthesis, binding affinity and intrinsic activity for MT(1) and MT(2) melatonin receptorsGilberto Spadoni, Annalida Bedini, Pierfrancesco Orlando, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|March 5, 2015
Pushing the boundaries of vinylogous reactivity: catalytic enantioselective mukaiyama aldol reactions of highly unsaturated 2-silyloxyindolesClaudio Curti, Andrea Sartori, Lucia Battistini, et al.Pageof 20