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Advances in Experimental Medicine and Biology|June 23, 2004
Strategies leading to MT2 selective melatonin receptor antagonistsGilberto Spadoni, Annalida Bedini, Giovanni Piersanti, et al.
Journal of Chemical Information and Modeling|April 2, 2013
Structure-based virtual screening of MT2 melatonin receptor: influence of template choice and structural refinementDaniele Pala, Thijs Beuming, Woody Sherman, et al.
Organic & Biomolecular Chemistry|October 11, 2012
Divergent synthesis of novel 9-deazaxanthine derivatives via late-stage cross-coupling reactionsFrancesca Bartoccini, Giovanni Piersanti, Marco Mor, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|July 14, 2021
Different roles for the acyl chain and the amine leaving group in the substrate selectivity of <i>N</i>-Acylethanolamine acid amidaseAndrea Ghidini, Laura Scalvini, Francesca Palese, et al.
Pharmacological Research|August 29, 2006
The fatty-acid amide hydrolase inhibitor URB597 does not affect triacylglycerol hydrolysis in rat tissuesJason R Clapper, Andrea Duranti, Andrea Tontini, et al.
Journal of Molecular Modeling|March 3, 2011
Application of a SCC-DFTB QM/MM approach to the investigation of the catalytic mechanism of fatty acid amide hydrolaseLuigi Capoferri, Marco Mor, Jitnapa Sirirak, et al.
Journal of Mass Spectrometry : JMS|December 4, 2004
Tandem mass spectrometric data-FAAH inhibitory activity relationships of some carbamic acid O-aryl estersElisa Basso, Andrea Duranti, Marco Mor, et al.
International Journal of Pharmaceutics|May 1, 2013
Complex product composition generates risks for generic substitution also with dosage forms for intravenous administrationAlessandra Rossi, Francesca Buttini, Paolo Colombo, et al.
Journal of Chemical Information and Modeling|April 13, 2023
Unbinding Kinetics of Muscarinic M3 Receptor Antagonists Explained by Metadynamics SimulationsFrancesca Galvani, Daniele Pala, Alberto Cuzzolin, et al.
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