Uresh Shah
Publications by Year
Research Areas
Synthesis and Biological Evaluation, Synthesis and Reactions of Organic Compounds, Synthesis and Reactivity of Heterocycles, Organic Chemistry Cycloaddition Reactions, Pharmacological Receptor Mechanisms and Effects
Most-Cited Works
- → Studies toward the discovery of the next generation of antidepressants. Part 5: 3,4-Dihydro-2H-benzo[1,4]oxazine derivatives with dual 5-HT1A receptor and serotonin transporter affinity(2005)49 cited
- → Pyrido[3',2':4,5]thieno[3,2-d]-N-triazines: a new series of orally active antiallergic agents(1984)40 cited
- → Structure-activity relationships among analogues of pemedolac, cis-1-ethyl-1,3,4,9-tetrahydro-4-(phenylmethyl)pyrano[3,4-b]indole-1-acetic acid, a potent analgesic agent(1988)29 cited
- → Advances toward New Antidepressants with Dual Serotonin Transporter and 5-HT1AReceptor Affinity within a Class of 3-Aminochroman Derivatives. Part 2(2008)27 cited
- → Azole Phenoxy Hydroxyureas as Selective and Orally Active Inhibitors of 5-Lipoxygenase(1996)22 cited
- → New generation dopaminergic agents. 7. Heterocyclic bioisosteres that exploit the 3-OH-phenoxyethylamine D2 template(1999)10 cited
- → Synthesis of 2-Dialkylaminomethyl-1,4-benzoxathians(1972)7 cited
- → Structure-activity relationships leading to WAY-121,520, a tris aryl-type, indomethacin-based, phospholipase A2 (PLA2)/leukotriene biosynthesis inhibitor(1993)4 cited
- → ChemInform Abstract: DIE SYNTH. VON 2‐DIALKYLAMINOMETHYL‐1,4‐BENZOXATHIANEN(1972)
- → ChemInform Abstract: New Generation Dopaminergic Agents. Part 7. Heterocyclic Bioisosteres that Exploit the 3‐OH‐Phenoxyethylamine D2 Template.(1999)