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American Journal of Respiratory and Critical Care Medicine|August 20, 2005
Acquired rifamycin resistance with twice-weekly treatment of HIV-related tuberculosisWilliam Burman, Debra Benator, Andrew Vernon, et al.ACS Central Science|August 13, 2019
Targeting the Chondroitin Sulfate Proteoglycans: Evaluating Fluorinated Glucosamines and Xylosides in Screens Pertinent to Multiple SclerosisErin L Stephenson, Ping Zhang, Samira Ghorbani, et al.Farmaco (Societa Chimica Italiana : 1989)|September 19, 2003
The role of HB-donor groups in the heterocyclic polar fragment of H3-antagonists. I. Synthesis and biological assaysValentina Zuliani, Fabrizio Bordi, Mirko Rivara, et al.Advances in Experimental Medicine and Biology|June 23, 2004
Antioxidant and cytoprotective activity of indole derivatives related to melatoninMarco Mor, Gilberto Spadoni, Giuseppe Diamantini, et al.Chemmedchem|June 26, 2009
Structure-property relationships of a class of carbamate-based fatty acid amide hydrolase (FAAH) inhibitors: chemical and biological stabilityFederica Vacondio, Claudia Silva, Alessio Lodola, et al.Journal of Medicinal Chemistry|April 4, 2003
Three-dimensional quantitative structure-activity relationship studies on selected MT1 and MT2 melatonin receptor ligands: requirements for subtype selectivity and intrinsic activity modulationSilvia Rivara, Marco Mor, Claudia Silva, et al.European Journal of Medicinal Chemistry|August 9, 2011
Biphenyl-3-yl alkylcarbamates as fatty acid amide hydrolase (FAAH) inhibitors: steric effects of N-alkyl chain on rat plasma and liver stabilityFederica Vacondio, Claudia Silva, Alessio Lodola, et al.Journal of Pineal Research|February 14, 2004
Indole-based analogs of melatonin: in vitro antioxidant and cytoprotective activitiesMarco Mor, Claudia Silva, Federica Vacondio, et al.Journal of Pineal Research|February 28, 2006
Synthesis, antioxidant activity and structure-activity relationships for a new series of 2-(N-acylaminoethyl)indoles with melatonin-like cytoprotective activityGilberto Spadoni, Giuseppe Diamantini, Annalida Bedini, et al.Chemistry & Biodiversity|January 22, 2008
Synthesis and stability in biological media of 1H-imidazole-1-carboxylates of ROS203, an antagonist of the histamine H3 receptorMirko Rivara, Federica Vacondio, Claudia Silva, et al.Pageof 19