Sharad S. Magar
Ono Pharmaceutical (United States)(US)
Publications by Year
Research Areas
Neuroscience and Neuropharmacology Research, Ion channel regulation and function, Chemical Synthesis and Analysis, Receptor Mechanisms and Signaling, Synthetic Organic Chemistry Methods
Most-Cited Works
- → Synthesis and Pharmacological Evaluation of N-(2,5-Disubstituted phenyl)-N‘-(3-substituted phenyl)-N‘-methylguanidines As N-Methyl-d-aspartate Receptor Ion-Channel Blockers(1997)83 cited
- → Synthesis and binding characteristics of N-(1-naphthyl)-N′-(3-[125I]-iodophenyl)-N′-methylguanidine ([125I]-CNS 1261): a potential SPECT agent for imaging NMDA receptor activation(2000)53 cited
- → Identification, synthesis, and biological evaluation of novel pyrazoles as low molecular weight luteinizing hormone receptor agonists(2006)40 cited
- → Synthesis of phorbol C-ring analogs: a biomimetic model study on the phorbol to 12-hydroxydaphnetoxin conversion.(1992)31 cited
- → Neuroprotective Use‐Dependent Blockers of Na+ and Ca2+ Channels Controlling Presynaptic Release of Glutamatea(1995)29 cited
- → Synthesis and Pharmacological Evaluation of N,N‘-Diarylguanidines as Potent Sodium Channel Blockers and Anticonvulsant Agents(1998)21 cited
- → N-(3-Azidophenyl)-N-methyl-N'-([4-1H]- and [4-3H]-1-naphthyl)guanidine. A potent and selective ligand designed as a photoaffinity label for the phencyclidine site of the N-methyl-D-aspartate receptor(1993)4 cited
- Novel N-substituted Imidazole based non-ATP competitive MEK inhibitors as potential anticancer agents(2007)
- The synthesis of phorbol C-ring analogs, a model study on the phorbol to 12-hydroxydaphnetoxin conversion, and other synthetic studies(1991)